bc Flashcards

1
Q

1.Which of the following amino acids supply the
atoms of positions 1,4,5 and 6 of the pyrimidine ring
in the de novo pyrimidine biosynthesis:
a) glycine
b) aspartate
2.c) glutamine
3.d) glutamate

A

aspartate

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2
Q

In which the following catabolic processes amino acids are converted to the
corresponding α keto-acids (C-skeletons).
1) oxidative deamination
2) degradation of the carbon backbone
3) transamination
4) decarboxylation
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

b. 1+3

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3
Q

Which of the following statements about the activation of the urea
cycle is
wrong:
a) urea cycle is activated during periods of fasting
b) the urea cycle is activated upon allosteric activation of the regulatory
enzyme (carbamoyl phosphate synthetase I) from N-acetyl-glutamate
c) the urea cycle is activated upon induction of the synthesis of enzymes
involved in the urea cycle
d) urea cycle is activated after meal with low protein content

A

d) urea cycle is activated after meal with low protein content

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4
Q

Which of the following cofactors serve as prosthetic groups of the
enzymes aminoacidooxidases which catalyze the oxidative deamination
of amino acids:
1) NAD+
2) FMN
3) NADP+
4) FAD
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

b) 1 + 3

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5
Q

For the synthesis of which of these molecules (neurotransmitters and
hormones) the amino acid tyrosine is not a precursor (substrate):
a) dopamine
b) serotonin
c) catecholamines (norepinephrine and epinephrine)
d) thyroid hormones

A

b) serotonin

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6
Q

Which of the following statements about the synthesis of heme in
mammalian cells is true?
a)succinyl CoA and alanine are direct substrates for the formation of 5-
aminolevulinic acid (5-Ala)
b) Ferric ions (Fe3 +) are introduced into protoporphyrin IX
c) Coproporphyrin IV is an intermediate metabolite
d) Porphobilinogen is formed due to the condensation of 2 molecules of
5- Ale

A

d) Porphobilinogen is formed due to the condensation of 2 molecules of
5- Ale

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7
Q

Patients with reduced intake of bilirubin from hepatocytes A) have an
increased level of “indirect” bilirubin in the blood B) have an increased
level of “direct” bilirubin in the blood
a) А
b) B
c) A and B
d) neither А nor B

A

d) neither А nor B

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8
Q

In enzyme defect (deficiency) 5-Ala dehydratase (porphobilinogen
synthase) the following clinical signs are observed:
a) severe abdominal pains thrusts or
b) skin photosensitivity

a) А
b) B
c) A and B
d) neither А nor B

A

b.b

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9
Q

In the synthesis of heme in mammalian cells:

1) Uroporphyrin III is the direct predecessor of coproporphyrin III
2) Ala-5 is formed by the condensation of succinyl CoA and valine
3) The ferric ion (Fe3 +) is introduced into the protoporphyrin IX before its
binding to globin molecule
4) Porphobilinogen formed due to the condensation of 2 molecules of 5-Ale
a)1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

b) 1 + 3

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10
Q

In the metabolism of iron:

1) during the passage of the ferrous ions (Fe2 +) from the enterocytes in the
blood they are oxidized to ferric ions (Fe3 +) under the action of
tserulopazmin
2) the main transport protein of iron in plasma is hemosiderin
3) in the form of a complex with the protein ferritin iron accumulates in the
cells of the intestinal mucosa, liver, bone marrow
4) almost all of the iron from the diet is absorbed and excess is excreted in
the faeces
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

b) 1 + 3

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11
Q

Increase in the blood of “direct” bilirubin is expected in:
1) hemolytic jaundice
2) low activity of Bilirubin-UDP-glucuronyl transferase as it is in infants
3) decreased hepatic intake of bilirubin (Gilbert syndrome)
4) biliary obstruction (blockage)
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

a) 1 + 2 + 3

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12
Q

Ale synthetase:

1) requires pyridoxalphosphate for its activation
2) the synthesis of the enzyme may be induced by phenobarbital and some
of the steroids
3) suppressed by catarrh
4) is inhibited by lead
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

a) 1 + 2 + 3

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13
Q

Thioredoxin is involved in:

a) the conversion of ATP into ADP
b) the conversion of dUMF into dTMF
c) the conversion of ribonucleotides into deoxyribonucleotides
d) the inhibition of xanthine oxidase

A

a) the conversion of ATP into ADP

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14
Q

Which of the following mechanisms performes control the de novo synthesis
of pyrimidine nucleotides in humans:

1) negative feedback of glutamine-PRPP-amidotransferase
2) negative feedback of aspartate transcarbamoylase
3) availability of N-acetyl glutamate
4) availability of PRPP
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

d) 4

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15
Q

Methotrexate is an inhibitor of dihydrofolate reductase. Its application
would inhibit:
1) de novo synthesis of UMP
2) conversion of dUMP into dTMP
3) conversion of IMP into GMP
4) de novo synthesis of IMP
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

c) 2 + 4

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16
Q

Aspartic acid plays a role in all of the following processes with the
exception of one. Which is it?

a) de novo synthesis of AMP
b) the conversion of ATP into CTP
c) de novo synthesis of orotic acid
d) maintaining the pool (reservoir) of adenine nucleotides through
alternative pathways

A

c) de novo synthesis of orotic acid

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17
Q

From the amino acid Trp (tryptophan) are obtained following biologically
important compounds

1) thyroxine
2) melanin
3) dopamine
4) melatonin
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

d) 4

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18
Q

End products of the N-metabolism, which are excreted from the body
are:
1) urea
2) creatine
3) uric acid
4) acetoacetate
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

a) 1 + 2 + 3

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19
Q

Metabolites of Ornithine cycle are:
1) succinyl CoA
2) citrulline
3) 5- Aminolevulinic acid
4) carbamoyl phosphate
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

c) 2 + 4

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20
Q

Pyrimidines degradation products are:
1) b-aminoisobutyrate
2) urea
3) b-alanine
4) orotic acid
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

d) 4

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21
Q

Regulatory enzymes of purines de novo synthesis are:
1) xanthine oxidase
2) PRPP amidotransferase
3) adenine phosphoribosyltransferase
4) adenilosuccinate synthetase
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

d.4

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22
Q

Which of the following enzymes is defective in patients with Lesch-Nyhan
syndrome?

a) adenosine deaminase
b) adenine phosphoribosyltransferase (АPT)
c) xanthine dehydrogenase (oxidase)
d)hypoxanthineguaninephosphoribosyltransferase (HGPRT)

A

d)hypoxanthineguaninephosphoribosyltransferase (HGPRT)

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23
Q

Which of the following groups of amino acids can be classified as “non-
essential”?

a) Ala, Glu, Ile, Pro
b) Asn, Cys, Pro, Tyr
c) Ast, Ser, Thre, Tyr
d) Ala, Gln, Gly, Trp

A

b) Asn, Cys, Pro, Tyr

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24
Q

Tetrahydrobiopterin is required to:
a) methylation of dUMP
b) degradation of Tyr
c) hydroxylation of phenylalanine
d) transfer of one-carbon groups (fragments)

A

c) hydroxylation of phenylalanine

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25
Q

Hereditary metabolic disorder known as Phenylketonuria (PKU):

a)is usually due to a hereditary defect of the enzyme phenylalanine
hydroxylase
b) is related to a high level of phenylalanine and tyrosine in blood
plasma
c) manifests in young boys
d) associated with blond hair and a light tan because phenylalanine
inhibits the production of melanin

A

a)is usually due to a hereditary defect of the enzyme phenylalanine
hydroxylase

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26
Q

Which of the following amino acids are precursors in the synthesis of
creatine phosphate?

1) Glycine
2) methionine
3) arginine
4) glutamine
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

b) 1 + 3

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27
Q

Transamination reactions require one of the following vitamins
a) riboflavin
b) pantothenate;
c) thiamine;
d) pyridoxol;

A

d) pyridoxol;

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28
Q

Which of the following vitamins is a precursor of prosthetic groups of
transaminases?

а) thiamine
b) pyridoxine
c) niacin
d) riboflavin

A

b) pyridoxine

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29
Q

In which of the following diseases is observed increased levels of
GOT(АsАТ)?.
1. obstructive jaundice
2. viral hepatitis
3. brain stroke
4. cardiac infarction
a) 1+2+3
b) 1+3
c) 3+4
d) 1+2+4

A

d) 1+2+4

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30
Q

Which of the following enzymatic defects is responsible for the Crigler-
Naijar syndrome?

а) argininosuktsinat synthetase deficiency
b) bilirubin UDP-glucuronyl-transferase deficiency
c) Pal-hydroxylase deficiency
d) biopterin synthase deficiency

A

b) bilirubin UDP-glucuronyl-transferase deficiency

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31
Q

Reactions of disposal of ammonia in peripheral tissues are
1) glutamine synthase reaction
2) urea synthesis
3) reductive amination of alpha-ketoglutarate
4) amidoacidooxidase reaction
a) 1 + 2 + 3
b) 1 + 3
c) 2 + 4
d) 4

A

b) 1 + 3

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32
Q

Which of the following compounds is obtained from tryptophan as one
of the reactions in its synthesis is a reaction of decarboxylation?
a) dopamine
b) melatonin
c) epinephrine
d) histamine

A

b) melatonin

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33
Q

Which of these amino acids is only ketogenic amino acid?
а) tryptophan
b) leucine
c) isoleucine
d) alanine

A

b) leucine

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34
Q

Which of the following enzymes catalyze reactions of disposal (fixing) of
ammonia?

  1. glutamate dehydrogenase
  2. carbamoyl phosphate synthetase
  3. glutamine synthetase
  4. glutaminase
    а) 1+2+3
    b) 2+3
    c) 2+4
    d) 1+2+4
A

c) 2+4

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35
Q

Which of the following reactions from Ornithine cycle is endergonic
and requires ATP?
а) ornithine transcarbamoylase
b) argininosuccynate synthetase
c) argininosuccynate lyase
d) arginase

A

c) argininosuccynate lyase

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36
Q

Which of the following compounds accumulate in the blood and is
excreted in the urine in argininosuccynate synthetase block?
a) arginine
b) argininosuccynate
c) citrulline
d) ornithine

A

a) arginine

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37
Q
  1. To which of the following metabolites some of glycogen amino
    acids are degraded?
  2. pyruvate
  3. acetoacetate
  4. oxaloacetate
  5. fumarate
    a) 1+2+3
    b) 2+3
    c) 2+4
    d) 1+3+4
A

d) 1+3+4

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38
Q

Which of these amino acids is only ketogenic amino acid?

а) tryptophan
b) leucine
c) isoleucine
d) alanine

A

b) leucine

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39
Q

In block of which of the following enzymes develops classical
phenylketonuria?

a) homogentisate oxidase
b) tyrosine transaminase
c) dihydrobiopterin reductase
d) phenylalanine hydroxylase

A

d) phenylalanine hydroxylase

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40
Q

Which of the following biologically important compounds are byproducts
from the metabolism of tryptophan?

  1. thyroxine
  2. melatonin
  3. melanin
  4. serotonin
    a) 1+2+3
    b) 2+3
    c) 2+4
    d) 1+3+4
A

c) 2+4

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41
Q

Which of the following enzymes involved in the synthesis of heme is the major
regulatory enzyme regulated by the type of feedback at the genetic level?

a) aminolevulinate dehydratase
b) aminolevulinate synthase
c) uroporphyrinogen III co-synthase
d) uroporphyrinogen decarboxylase

A

b) aminolevulinate synthase

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42
Q

Which of the following biologically important compounds are byproducts
from the metabolism of tyrosine?

  1. thyroxine
  2. melatonin
  3. melanin
  4. dopamine
    a) 1+2+3
    b) 2+3
    c) 2+4
    d) 1+3+4
A

d) 1+3+4

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43
Q

Which of the following one-carbon groups bind to tetrahydrofolic acid
(FAH4) is the most reduced (C atom has the lowest oxidation state)?

a) formyl (N10- formyl -FAН4)
b) methyl (N5- methyl -FAН4)
c) methylene (N5 ,N10- methylene -FAН4)
d) formimine (N5- formimine -FAН4)

A

b) methyl (N5-methyl-FAH4)

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44
Q

Which of the following compounds are byproducts, not precursors in the
synthesis of heme?

  1. 5-Aminolevulinic acid
  2. coproporphyrinogen I
  3. porphobilinogen
  4. uroporphyrinogen I
    a) 1+2+3
    b) 2+4
    c) 2+3
    d) 1+3+4
A

b) 2+4

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45
Q

Which of the following substituents and sequence of these substituents at
pyrrole ring are found in the precursor of heme coproporphyrinogen?
A – acetyl
P – propionyl
M – methyl
V - vinyl
a) MB МV МP PМ
b) МP МP МP МP
c) МP МP МP PМ
d) АP АP АP PА

A

d) АP АP АP PА

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46
Q
  1. In which the following catabolic pathways of amino acids “biogenic
    amines” are produced as end products:
    a) oxidative deamination
    b) transamination
    c) cleavage of the carbon backbone
    d) decarboxylation
A

a) oxidative deamination

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47
Q

Which of the following enzymes are involved in the degradation of
heme and the production of unconjugated bilirubin?

1) UDP- glucuronyl transferase
2) hemoxigenase
3) biliverdin reductase
4) bilirubin monoglucuronide mutase
a) 1+2+3
b) 2+4
c) 2+3
d) 1+3+4

A

c) 2+3

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48
Q

Defect (complete absence of activity) of which of the following

enzymes is responsible for the development of the disease Crigler-
Najjar I?

а) UDP- glucuronyl transferase
b) hemoxigenase
c) biliverdin reductase
d) bilirubin monoglucuronide mutase

A

а) UDP- glucuronyl transferase

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49
Q

Which of the following compounds is a bile pigment found in the urine
in mechanical (obstructive) jaundice?
a) urobilinogen
b) sterkobilinogen
c) conjugated bilirubin
d) unconjugated bilirubin

A

c) conjugated bilirubin

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50
Q

Considering that the zymogen forms represent the inactive enzyme
digesting dietary proteins, which of the following zymogens is not
converted into active enzyme by the action of trypsin:
a) chymotrypsinogen
b) pepsinogen
c) proelastase
d) procarboxypeptidase

A

b) pepsinogen

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51
Q

Which of the processes listed below is not endergonic?

А. muscle contraction
B. transportation of compounds along the concentration gradient
C. transmission of a nerve impulse
D. maintaining of a concentration gradient

A

D. maintaining of a concentration gradient

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52
Q

Which of the following statements related to the Second law of the
Thermodynamics is wrong?

A. Naturally all processes proceed in the direction leading to a maximum disorder.
B. A system is in equilibrium (is most stable) when the Enthalpy has a maximum value
C. The systems in equilibrium have maximum Entropy.
D. The magnitude, characterizing the change of energy that can do work is the Free energy

A

B. A system is in equilibrium (is most stable) when the Enthalpy has a
maximum value

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53
Q

The standard redox potentials (Ео’) of the redox systems NAD+/NAD.H and
pyruvate/lactate are: Eo = -0,32 V and Eo = -0,19 V, respectively. Which of the following
statements is wrong?

A. Under standard conditions, pH 7 and equimolar concentration of 1M of all
components of the systems, the redox system NAD+/NAD.H has a greater ability to
give electrons than the redox system pyruvate/lactate.
B. Under standard conditions, pH 7 and equimolar concentrations of 1M of all the
substances, the electrons flow from NAD.H to pyruvate.
C. If at the beginning of the reaction the concentration of all substances is 1M, and the
pH=7, the reversible reaction: pyruvate + NAD.H+H+ lactate + NAD+, will run from
left to right
D. If at the beginning of the reaction the concentration of all substances is 1M, and the
pH=7, the reversible reaction: pyruvate + NAD.H+H+ lactate + NAD+, will run from
right to left

A

B. Under standard conditions, pH 7 and equimolar concentrations of 1M of all the
substances, the electrons flow from NAD.H to pyruvate.

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54
Q

When you consider the standard redox potentials (Eo’) on
these three redox systems:

1) Cytochrome.b6 (Fe3+)/ Cytochrome b6 (Fe2+) - Eo’= - 0,06V
2) Cytochrome f (Fe3+)/ Cytochrome f (Fe2+) - Eo= + 0,365V
3) Ferredoxin (oxidized)/ Ferredoxin (reduced) - Eo= - 0,432V
which of the following redox chains is correct? А. 1, 2, 3
B. 1,3,2
C. 3, 2, 1
D. 3, 1, 2

A

C. 3, 2, 1

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55
Q
  1. Which of the following bonds are rich in energy (macroergic)?
    1) thioester bonds
    2) phosphosulfate bonds
    3) pyrophosphate bonds
    4) phosphodiester bonds
    А: 1+2+3
    B: 1+3
    C: 2+4
    D: all four
A

D: all four

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56
Q
  1. Which of these magnitudes and values determine the standard free energy of an
    oxidoreductase process?

1) The number of electrons transferred during the reaction
2) The Faraday constant (F)
3) The difference between the normal redox potentials of redox systems 4) The
universal gas constant (R)
А: 1+2+4
B: 1+3+4
C: 1+2+3
D: all four

A

B: 1+3+4

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57
Q
  1. Which of the following types of oxidoreductases have most
    often Vit B2 derivatives as cofactors?

A. Peroxidases
B. Oxidase
C. Monooxygenase
D. Anaerobic dehydrogenases

A

B. Oxidase
C. Monooxygenase

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58
Q
  1. Which of the following enzymes is involved in the elimination of
    H2O2?
  • A: Glutathione peroxidase
  • B: Superoxide dismutase
  • C: Glutathione reductase
  • D: Ham oxygenase
A
  • A: Glutathione peroxidase
  • B: Superoxide dismutase
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59
Q
  1. The listed cytochromes are involved in the respiratory chain in mitochondria.
    There is only one exception. What is that exception?

А: Cytochrome с1
B: Cytochrome с
C: Cytochrome b5
D: Cytochrome а3

A

C: Cytochrome b5

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60
Q
  1. Which of the listed redox systems of biological interest is a quinine
    redox system?

A: NAD+/NAD.H
B: Glutathione
C: Vitamin С
D: Coenzyme Q

A

A: NAD+/NAD.H

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61
Q
  1. Which of the listed redox systems of biological interest is a thiol
    redox system?
    А: Glutathione
    B: FAD
    C: NAD+
    D: Vitamin С
A

D: Vitamin С

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62
Q

Which of the following oxidoreductases function only as
anaerobic dehydrogenases?

А: the enzymes cooperated with flavonic redox system (FAD or FMN)
B: the enzymes cooperated with nicotinamide redox systems (NAD+ or NADP+)
C: oxidases
D: oxygenases

A

B: the enzymes cooperated with nicotinamide redox systems (NAD+ or NADP+)

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63
Q

Which of the following oxidoreductases are monooxygenases?
1) Cytochrome oxidase
2) Phenylalanine hydroxylase
3) Tryptophan oxygenase
4) Tryptophan hydroxylase
A: 1+2+3
B: 1+3
C: 2+4
D: only 4

A

C: 2+4

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64
Q

Which of the following substances are direct hydrogen donors in the
processes catalyzed by peroxidases for elimination of H2O2 and/or
hydroperoxides?

1) Ascorbic acid (Vit С)
2) Tocopherols (Vit E)
3) Glutathione
4) NADP.H
А: 1+2+3
B: 1+3
C: 2+4
D: all four

A

B: 1+3

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65
Q

Which of the following substances is a specific inhibitor of the
electron transport performed by the complex IV of the respiratory
chain?

A. Oligomycin
B. Atractiloside
C. Malonate
D. CO

A

D. CO

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66
Q

Which of the listed process in the respiratory chain will be inhibited
in the presence of the antibiotic oligomycin?

A. Cell respiration (redox processes in the respiratory chain)
B. Transfer of phosphate ions through the inner mitochondrial
membrane
C. Transfer of ADP/ATP through the inner mitochondrial membrane
D. Synthesis of ATP

A

D. Synthesis of ATP

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67
Q

Indicate which of the following inhibitors of oxidative
phosphorylation in respiratory chain inhibite the transport across the
inner mitochondrial membrane of ATP and ADP:

А: Atractyloside
B: Rotenone
C: Oligomycin
D: Malonate

A

C: Oligomycin

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68
Q

The truncated (short) electron transport chains involved in the
process of hydroxylation with Cytochrome P450 (CYP) are located
mainly in one type of the listed subcellular structures. Which are those
structures?

А: lysosomes
B: peroxisomes
C: nuclei
D: endoplasmic reticulum

A

D: endoplasmic reticulum

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69
Q

Indicate which of the following compounds is an uncoupling agent
of oxidative phosphorylation in the respiratory chain?

А: Rotenone
B: 2,4-dinitrophenol
C: Oligomycin
D: Atractyloside

A

C: Oligomycin

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70
Q

All listed enzymes, except for only one type, are flavoproteins
(FAD/FMN-associated dehydrogenases):

A: D-amino acid oxidase
B: malate dehydrogenase
C: NAD+-dehydrogenase
D: succinate dehydrogenase

A

B: malate dehydrogenase

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71
Q

Which of the following processes are processes of “free oxidation”:

1: hydroxylation with Cytochrome Р450 (CYPs)
2: oxidation of glyceraldehyde 3-phosphate
3. oxidative deamination of amino acids
4: oxidation of lactate
A: 1+2+3
B: 1+3
C: 2+4
D: none of them

A

D: none of them

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72
Q

Which of the listed processes leads to elimination of the superoxide
anion radicals:

А: reaction catalyzed by NADPH-oxidase
B: spontaneous oxidation of hemoglobin
C: reaction catalyzed by superoxide dismutase
D: reaction catalyzed by xanthine oxidase

A

C: reaction catalyzed by superoxide dismutase

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73
Q
  1. In which of the listed subcellular structures the enzyme catalase is
    localized?

А: peroxisomes
B: lysosomes
C: mitochondria
D: nuclei

A

А: peroxisomes

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74
Q

Which of the following statements concerning ubiquinone (Q) is wrong?

A: In its reduced form, the coenzyme Q (ubiquinone) reacts with Fe-S complexes of ubiquinone- cytochrome c oxidoreductase and transfers one electron on them.
B: The quinone structure of the molecule can bind one electron forming condition
called free radical semiquinone.
C: In the respiratory chain it is reduced by the ubiquinone-cytochrome c
oxidoreductase and is oxidized by cytochrome c oxidase
D: In mammals its molecule typically has a hydrophobic “tail” made up of 10
isoprene residues

A

A: In its reduced form, the coenzyme Q (ubiquinone) reacts with Fe-S complexes of ubiquinone- cytochrome c oxidoreductase and transfers one electron on them.

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75
Q

NAD+ and Ubiquinone (Q) serve as collectors of reducing equivalents released
during the dehydrogenation of a variety of substrates. These reducing equivalents
further are transmitted from reduced ubiquinone (QH2) in the respiratory chain to
cytochromes. Indicate which of the listed metabolites are oxidized in the
mitochondria yielding NAD.H, which is a major substrate of respiratory chain.

1: isocitrate
2: glycerol-3-phosphate
3. malate
4: succinate
A: 1+2+3
B: 1+3
C: 2+4
D: all four

A

B: 1+3

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76
Q

All lised chemical bonds are macroergic except one. Which is that
bond?:

А: Pyrophosphate bond
B: Thioester bond
C: Enolphosphate bond
D: Glycosidic bond

A

D: Glycosidic bond

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77
Q

Which of the following processes are processes of free oxidation:

1: hydroxylation with Cytochrome Р450 (CYPs)
2: oxidation of hypoxanthine
3. oxidative deamination of amino acids
4: oxidation of glyceraldehyde 3-phosphate
A: 1+2+3
B: 1+3
C: 2+4
D: none of them

A

D: none of them

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78
Q

Which of the following substances carry out their antioxidant function
mainly by reduction of tocopheryl radical to tocopherol?

1: b-carotene
2: Vitamin C
3: Vitamin A
4: flavonoids
A: 1+2+3
B: 1+3
C: 2+4
D: all of them

A

B: 1+3

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79
Q

Which of the listed processes does not lead to production of
superoxide anion radical:

A: reaction catalyzed by NADPH-oxidase
B: spontaneous oxidation of hemoglobin
C: reaction catalyzed by superoxide dismutase
D: reaction catalyzed by xanthine oxidase

A

C: reaction catalyzed by superoxide dismutase

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80
Q

Choose the correct statement, referring to the eukaryotic
mitochondrial ATP synthase complex

A: ATP from ADP and inorganic phosphate (Pi) is synthesized in the F1 fragment
B: The electron microscopic observations show that the F1 fragment of the
complex binds to the transmembrane Fo fragment and it is placed on the outer side of the inner mitochondrial membrane
c: The antibiotic oligomycin binds the Fo fragment and inhibits the flow of H+
out of mitochondria
D: The synthesis of ATP is carried out in the F1 fragment of the complex, and
it is a result of oxidative phosphorylation of substrate level

A

c: The antibiotic oligomycin binds the Fo fragment and inhibits the flow of H+ out of mitochondria

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81
Q

The adding of 2,4-dinitrophenol to the active “breathing”
mitochondria causes the effects given below except one of them.
Which is that exception?

А: [NAD+] is increased
B: There is enhancement of ATP production
C: There is enhancement of О2 consumption
D: Annulling of proton (H+) gradient

A

B: There is enhancement of ATP production

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82
Q

Indicate which of these cytochromes are not involved in the
truncated (microsomal) electron- transfer chains:

1: Cytochorme b5
2: Cytochrome c
3: Cytochrome Р450
4: Cytochrome а3
А: 1+2+3
B: 1+3
C: 2+4
D: all of them

A

C: 2+4

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83
Q

Which of the following statements concerning respiratory chain is
wrong?

A: Ubiquinone is a lipid-soluble component of respiratory chain.
B: The reduction of molecular O2 is performed in Cytochrome c oxidase
complex.
C: The arrangement of the redox systems in respiratory chain enables the transmission of electrons from NAD.H+H+ and FAD.H2 to O2, which otherwise is thermodynamically impossible
D: The two enzymes: NAD.H - dehydrogenase and Succinate
dehydrogenase transfer electrons to coenzyme Q (ubiquinone).

A

C: The arrangement of the redox systems in respiratory chain enables
the transmission of electrons from NAD.H+H+ and FAD.H2 to O2, which
otherwise is thermodynamically impossible

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84
Q

Which of the following statements related to Cytochrome c is
wrong?

A: It has a standard redox potential lower than Cytochrome a3
B: Binds one electron and becomes oxidized
C: Participates in redox processes by transferring one electron
D: Connects protein complexes III and IV in respiratory chain

A

A: It has a standard redox potential lower than Cytochrome a3

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85
Q

Choose the wrong statement concerning chemioosmotic mechanism for coupling of
oxidation in respiratory chain and phosphorylation of ADP.

A: The main protein complexes of respiratory chain in mitochondria carry out pumping H+
from the matrix into intermembrane space.
B: The transmembrane pH gradient in mitochondria may be reduced and annulled by DNP
(2,4- dinitrophenol), which brings protons across the inner membrane
C. The pH within the mitochondrial matrix is lower than in the intermembrane space of mitochondria.
D: The energy of the electrochemical H+ gradient across the inner mitochondrial membrane
is the one that drives the synthesis of ATP

A

C. The pH within the mitochondrial matrix is lower than in the intermembrane space of mitochondria.

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86
Q

Which of the following statements is wrong?

A: The change of the free energy that is released as a result of the hydrolysis of 1 mol ATP to 1 mol ADP and 1 mol inorganic phosphate (Pi) is 30.5 kJ (7 kkal).
B: Thermodynamically unfavorable reactions (endergonic) may occur
due to conjugation with thermodynamically favorable (exergonic)
reactions
C: In equilibrium free energy change G is always <0
D: The total change of free energy of chemically coupled processes is equal to the sum of the changes of the free energy of each of the reactions.

A

C: In equilibrium free energy change G is always <0

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87
Q

Free oxidation is important for some of the processes listed below. Which
are they?

1) thermogenesis
2) synthesis of steroid hormones
3) metabolism of xenobiotics
4) metabolism of aromatic amino acids
А: 1+2+3
B: 1+3
C: 2+4
D: all four

A

B: 1+3

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88
Q

Which of the following characteristics and functions are not specific
for ubiquinone (coenzyme Q)?

A collector of reducing equivalents
B. uncoupling of oxidative phosphorylation in the respiratory chain
C. transfer of H+ in membranes - mitochondrial, lysosomal, plasma
membrame
D. antioxidant role

A

B. uncoupling of oxidative phosphorylation in the respiratory chain

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89
Q

The following features are characteristical of the brown adipose
tissue. The exception is one of them. Which is that?

A. The tissue is highly vascularized.
B. There is high activity of ATP-synthase
C. The adipocytes are small, polygonal and have many mitochondria
with a large amount of cytochromes
D. In inner mitochondrial membrane a protein called termogenin is
localized which has a role of proton channel.

A

B. There is high activity of ATP-synthase

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90
Q

The Fo-F1 complex in mitochondria is important for one of the
following processes. Which is that?

А: Oxidation of NAD.Н to NAD+
B: Obtaining of ATP from AMP and Pi
C: Transport of Н+ out of the mitochondria
D: Obtaining of ATP from AMD and Pi

A

D: Obtaining of ATP from AMD and Pi

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91
Q

Which of the following statements is true?

A: In respiratory chain Cytochrome c can transfer simultaneously 2
electrons
B: The compound, 2,4-dinitrophenol, uncouples the oxidative
phosphorylation by annulling the H+ gradient on both sites of the inner
mitochondrial membrane
C: CN- inhibit Cytochrome c.
D: The chemical substances, rotenol and amitalat, specifically inhibit
cytochrome oxidase

A

C: CN- inhibit Cytochrome c.

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92
Q

Which of the following statements is true for chemiosmotic hypothesis of
Mitchell?

A: There is chemical conjugation (coupling) of oxidation of NAD.H with ATP
synthesis
B: There is synthesis of ATP during the flow of H+ along their concentration
gradient across the inner mitochondrial membrane to the matrix
C: There is formation of macroergic intermediate compound during
transmission of eletrons
D: There is generation of pH gradient on both sides of the outer
mitochondrial membrane

A

B: There is synthesis of ATP during the flow of H+ along their concentration
gradient across the inner mitochondrial membrane to the matrix

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93
Q

Which of the following compounds contain macroergic bonds and are
macroergic?

1: enolphosphate
2: succinyl-CoA
3: 1,3- bisphosphoglycerate
4: AMP
a: 1+2+3
b: 1+3
c: 2+4
d: all four

A

d: all four

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94
Q

The free energy obtained in respiratory chain can be used in
mitochondria for one of the following processes.

А: generation of heath
B: transport of ions
C: ATP synthesis
D: all of the above

A

C: ATP synthesis

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95
Q

Which of the following statements concerning the synthesis of ATP
in the mitochondria is not true?

A: ATP-synthase is oligomeric protein comprising 3 domains - transmembrane, intramatrix and associated domains
B: ATP synthase has oligomycin binding site

C: ATP-synthase is inhibited directly from CN-
D: ATP synthase catalyses the phosphorylation of ADP when H+ flows

through the complex from intermembrane space to the the
mitochondria

A

C: ATP-synthase is inhibited directly from CN-

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96
Q

Which of the following statements related to Cytochrom c is
wrong?

A: It is the only electron-transport protein that can be physically
separated from the inner mitochondrial membrane
B: It has a standard redox potential lower than Cytochrom a3
C: Participates in the process of apoptosis
D: Connect protein complex II and III of respiratory chain

A

D: Connect protein complex II and III of respiratory chain

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97
Q

Which of the following processes are involved in the process of heat production in cold
weather effects?

1) There is stimulation of the synthesis and secretion of thyroid hormones and noradrenaline
2) There is stimulation of lipolysis in adipose tissue
3) There is activation of adenylate cyclase, protein kinase A and hormone-sensitive lipase
4) There is coupling of the cellular respiration and oxidative phosphorylation
А: 1+2+3
B: 1+3
C: 2+4
D: all four

A

А: 1+2+3

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98
Q

Which of the following enzymes, involved in the breakdown of carbohydrates
in the digestive tract of humans, has/have small intestine origin?

1) sucrase
2) glucoamylase 3) lactase
4) α- amylase
a)1+2+3
b)1+3
c)2+4
D) 4

A

b)1+3

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99
Q

The absorption of glucose through the mucous membrane of
enterocytes in the human is performed via one of the listed types of
transport proteins. Which is that?

a) glucose transporter type 2 (GLUT2)
b) glucose transporter type 5 (GLUT5)
c) Na-dependent glucose transporter (SGLT1)
d) glucose transporter type 1 (GLUT1)

A

c) Na-dependent glucose transporter (SGLT1)

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100
Q

Which of the following co-enzymes does not participate in the pyruvate
dehydrogenase complex:

a) pyridoxalphosphate
b) thiamine pyrophosphate
c) coenzyme-A
d) lipoic acid

A

a) pyridoxalphosphate

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101
Q

Which of the following enzymes involved in the glycolysis is the major
regulatory enzyme of this pathway:

a) Phosphofructokinase-2 (PFK-2)
b) Aldolase
c) Phosphoglycerate kinase
d) Phosphofructokinase-1 (PFK-1)

A

a) Phosphofructokinase-2 (PFK-2)

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102
Q

Which of the following metabolites is not an allosteric modulator of the
main regulatory enzyme of glycolysis:

a) ATP
b) Glucose-6-phosphate
c) AMP
d) Fructose-2,6-bisphosphate

A

b) Glucose-6-phosphate

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103
Q

In which of the following cells the anaerobic glycolysis is performed:

1) white muscle fibers (during active contraction)
2) cells of the renal medulla
3) erythrocytes
4) cells of the eye lens
a) 1+2+3
b) 1+3
c) 2+4
d) 1+2+3+4

A

b) 1+3

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104
Q

Which of the following substances is a direct product of the action of
the enzyme glycogen phosphorylase (glycogenolysis):

a) Glucose-6-phosphate
b) Glucose
c) Glucose-1-phosphate
d) None of the mentioned above

A

c) Glucose-1-phosphate

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105
Q

Which of the following enzyme catalyzes the conversion of glucose to
glucose-6-phosphate in muscle cells:

a) Glucose-6-phosphatase
b) Glucokinase
c) Phosphoglucomutase
d) Hexokinase

A

d) Hexokinase

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106
Q

Which of the following enzymes uses NAD.H as coenzyme in reduction
process in anaerobic glycolysis:

a) Pyruvate kinase
b) Enolase
c) Lactate dehydrogenase
d) Glyceraldehyde-3-phosphate dehydrogenase

A

c) Lactate dehydrogenase

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107
Q

Which of the following statements about the malate-aspartate shuttle
is not true:

a) The shuttle is bidirectional
b) Cytoplasmic and mitochondrial malate dehydrogenases participate in the
shuttle
c) The oxidation in the respiratory chain of the two pairs of reducing
equivalents transferred by the shuttle mechanism, leads to the synthesis of
4 ATP molecules
d) The pair of substrates involved in the shuttle are oxaloacetate and malate

A

c) The oxidation in the respiratory chain of the two pairs of reducing
equivalents transferred by the shuttle mechanism, leads to the synthesis of
4 ATP molecules

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108
Q

Select the correct answer of the question: In how many ATP molecules
the energy released from the anaerobic glycolysis is accumulated?

a) Two
b) Eight
c) Thirty six
d) Four

A

a) Two

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109
Q

Which of the following enzymes are involved in the first, non-oxidizing
phase of the glycolytic pathway?

1) phosphohexosoisomerase
2) phosphofructokinase 1
3) hexokinase
4) enolase
a) 1+2+3
b) 1+3
c) 2+4
d) All of the mentioned above

A

a) 1+2+3

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110
Q

Which of the following enzymes catalyzes the synthesis of
fructose-2,6-bisphosphate, appearing as the strongest
activator of the regulatory enzyme of glycolysis:

a) Hexokinase
b) Phosphofructokinase 2
c) Phosphoglycerate kinase
d) Phosphofructokinase 1

A

b) Phosphofructokinase 2

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111
Q

Which of the following metabolic pathways of glucose supplies
reducing equivalents for the synthesis of fatty acids, cholesterol and
other reductive processes.

a) Glycolysis
b) Gluconeogenesis
c) Pentose phosphate pathway
d) Oxidative decarboxylation of pyruvate

A

c) Pentose phosphate pathway

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112
Q

Which of the following hormones has an effect on the liver cells,
resulting in the formation of active dephosphorylated kinase form of
the enzyme phosphofructokinase 2:

a) Glucagon
b) Adrenaline
c) Insulin
d) None of the mentioned above

A

c) Insulin

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113
Q

Which of the following enzymes of the glycolytic pathway catalyzes the
step, which is a oxidative phosphorylation at the substrate level, ie
carries out the synthesis of ATP when a metabolite is oxidized:

a) Phosphofructokinase 1
b) Hexokinase
c) Pyruvate kinase
d) Phosphoglucomutase

A

c) Pyruvate kinase

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114
Q

Which of the listed deficiencies (of enzymes and/or vitamins) lead to
lactic acidosis?

1) thiamine
2) erythrocyte enzymes of glycolysis
3) enzymes of pyruvate dehydrogenase complex
4) muscle enzymes of glycolysis
a) 1+2+3
b) 1+3
c) 2+4
d) All of the mentioned above

A

d) All of the mentioned above

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115
Q

Which of the following statements about the pentose
phosphate pathway of glucose is wrong:

a) It is performed actively in skeletal muscle
b) Supplies NADPH for fatty acid, cholesterol
biosynthesis etc..
c) The acyl-CoA derivatives inhibit the regulatory
enzyme
d) In the first (oxidation) step of the process 2
molecules NADPH are obtained

A

c) The acyl-CoA derivatives inhibit the regulatory

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116
Q

The risk of hemolytic anemia is associated with the deficiency of one of
the following enzymes of the pentose-phosphate pathway. Which is
that enzyme?

a) Transketolase
b) Phosphogluconolaktonase
c) Glucose-6-phosphate dehydrogenase
d) Transaldolase

A

c) Glucose-6-phosphate dehydrogenase

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117
Q

Which of the following enzymes of the glycolytic pathway is regulated
by a covalent modification:

a) Pyruvate kinase
b) Phosphofructokinase 1
c) Aldolase
d) Phosphoglucomutase

A

a) Pyruvate kinase

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118
Q

The failure of which of these enzymes involved in the catabolism of
fructose results into the hereditary disease “congenital fructose
intolerance”:

a) Fructokinase
b) Aldolase B
c) Ttriosokinase
d) none of the above mentioned

A

b) Aldolase B

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119
Q

Which of the following enzymes of gluconeogenesis does not use
energy of ATP, but of GTP.

a) pyruvate carboxylase
b) phosphoglycerate kinase
c) glucose-6-phosphatase
d) phosphoenolpyruvate-carboxykinase (PEPKK)

A

d) phosphoenolpyruvate-carboxykinase (PEPKK)

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120
Q

Which of the following co-enzymes serve as such of the enzyme of the
pentose phosphate pathway, transketolase, and by measuring the
enzymatic activity of transketolase is diagnosed a possible deficiency of
this vitamin in the body:

a) pyridoxal phosphate
b) thiamine pyrophosphate
c) NADP
d) FAD

A

b) thiamine pyrophosphate

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121
Q

In which of the following types of cells the transport of glucose is
insulin-independent:

1) adipocytes
2) brain
3) skeletal muscle cells
4) erythrocytes
a) 1+2+3
b) 1+3
c) 2+4
d) None of the above mentioned

A

c) 2+4

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122
Q

Which of the following statements about the pentose phosphate
pathway in mature erythrocytes is true:

a) Provides ribose-5-phosphate for the synthesis of nucleotides
b) Provides NADPH for fatty acid synthesis
c) Provides NADPH for maintaining the level of reduced glutathione, necessary for the disposal of Н2О2
d) Provides NADPH of cholesterol synthesis

A

c) Provides NADPH for maintaining the level of reduced glutathione, necessary
for the disposal of Н2О2

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123
Q

Which of the following metabolites serve as substrates for the synthesis
of glucose in the gluconeogenesis:

1) pyruvate
2) oxaloacetate
3) glycerol
4) acetyl-CoA
a) 1+2+3
b) 1+3
c) 2+4
d) All of the above mentioned

A

a) 1+2+3

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124
Q

Which of the following statements about the transport of glucose from
the blood into the cells of skeletal muscle is wrong:

a) the transport is carried out by a glucose transporter (facilitated diffusion)
b) insulin stimulates glucose transport through the export of glucose carriers
on the cell membrane, i.e. by increasing the number of transporters on the
cell membrane
c) the glucose enters the cells of the skeletal muscle along the concentration
gradient
d) Insulin induces the biosynthesis of an enzyme which catalyzes
phosphorylation of the free glucose to glucose-6-phosphate

A

c) the glucose enters the cells of the skeletal muscle along the concentration
gradient

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125
Q

Which of the following enzymes involved in gluconeogenesis, is the
most important regulatory enzyme in the process, subjected to
allosteric regulation of variety of modulators:

a) pyruvate carboxylase
b) glucose-6-phosphatase
c) fructose-1,6-bisphosphatase
d) phosphoenolpyruvate-carboxykinase (PEPKK)

A

c) fructose-1,6-bisphosphatase

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126
Q

Which of the following hormones stimulates the gluconeogenesis by
inducing biosynthesis of phosphoenolpyruvate-carboxykinase (PEPKK)
and other specific enzymes of gluconeogenesis:

a) Cortisol
b) Insulin
c) Aldosterone
d) Adenocorticotropic hormone (ACTH)

A

a) Cortisol

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127
Q

Which of the following metabolites of the citrate cycle can be directly
converted to phosphoenolpyruvate, and thus be incorporated into the
gluconeogenesis:

a) Citrate
b) Oxaloacetate
c) α– -Ketoglutarate
d) Fumarate

A

b) Oxaloacetate

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128
Q

Which of the following enzymes involved in the catabolism of galactose

catalyze the metabolic step of the conversion of galactose to galactose-
1-phosphate

a) Galactose-1-phosphate uridyltransferase
b) UDF- galactose-4-epimerase
c) Galactokinase
d) Phosphoglucomutase

A

c) Galactokinase

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129
Q

Which of the following enzymes functioning in gluconeogenesis, is
allosterically activated by Acetyl-CoA:

a) Glucose-6-phosphatase
b) Fructose-1,6-bisphosphatase
c) Phosphoenolpyruvate-carboxykinase (PEPKK)
d) Pyruvate carboxylase

A

d) Pyruvate carboxylase

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130
Q

Which of the activated forms of glucose is used as a direct substrate for
the synthesis of glycogen:

a) Glucose-6-phosphate
b) Glucose-1-phosphate
c) UDP-glucose
d) None of the above mentioned

A

c) UDP-glucose

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131
Q

Which of these metabolites is the allosteric activator of phosphorylated
glycogen synthase b:

a) АTP
b) АМP
c) glucose-6-phosphate
d) fructose-2,6-bisphosphate

A

c) glucose-6-phosphate

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132
Q

Which of the following statements about the metabolism of liver
glycogen is true:

a) During its degradation lactate is released in the blood
b) Glucagon stimulates its synthesis
c) It is broken down during the periods of fasting
d) adrenaline stimulates its synthesis

A

c) It is broken down during the periods of fasting

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133
Q

Glycerol is a non-carbohydrate precursor for the synthesis of glucose in
gluconeogenesis. To which of the listed metabolites of gluconeogenesis
turns the glycerol to:

a) Pyruvate
b) Dihydroxyacetone phosphate
c) Phosphonenolpyruvate
d) Fructose-6-phosphate

A

b) Dihydroxyacetone phosphate

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134
Q

Which of the following metabolic steps of gluconeogenesis is common
for glycolysis and gluconeogenesis:

a) fructose-6-phosphate → Glucose-6-phosphate
b) pyruvate →oxaloacetate
c) fructose-1,6-bisphosphate → fructose-6-phosphate
d) oxaloacetate → phosphonenolpyruvate

A

b) pyruvate →oxaloacetate

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135
Q

In which of the following organs the gluconeogenesis is performed:

1) liver
2) small intestine
3) renal cortex
4) skeletal muscles
a) 1+2+3
b) 1+3
c) 2+4
d) All of the above mentioned

A

b) 1+3

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136
Q

Alcohol (ethanol) inhibits the gluconeogenesis. Which of the following
statements about the inhibitory effect of ethanol is wrong:

a) oxidation of the ethanol leads to an increased level of NAD.H in hepatocytes
b) the high levels of NAD.H direct the lactate dehydrogenase reaction to the
conversion of pyruvate to lactate, which lowers the concentration of
pyruvate as a precursor of gluconeogenesis.
c) ethanol itself serves as inhibitor of the enzymes involved in
gluconeogenesis.
d) ethanol decreases the concentration of other substrates for
gluconeogenesis, in pyruvate (e.g., oxaloacetate)

A

d) ethanol decreases the concentration of other substrates for
gluconeogenesis, in pyruvate (e.g., oxaloacetate)

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137
Q

Which of the following statements about the effects of cortisol on the
blood glucose level is correct:

a) cortisol increases blood glucose level by stimulating the glycogenolysis
b) cortisol increases blood glucose level by stimulating gluconeogenesis
c) cortisol decreases blood glucose level by increasing the uptake of glucose
into cells
d) cortisol decreases blood glucose level by stimulating the glycolysis

A

b) cortisol increases blood glucose level by stimulating gluconeogenesis

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138
Q

Which of the following enzymes involved in glycogen metabolism,
catalyzes the phosphorolytic breakdown of α-1,4-glycosidic bond:

a) glycogen synthase
b) glycogen phosphorylase
c) phosphoglucomutase
d) amylo-1,4 → 1,6-transglycosylase

A

b) glycogen phosphorylase

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139
Q

Which of the following statements about the metabolism of liver
glycogen is wrong:

a) it is synthesized after carbohydrate-rich food intake
b) insulin stimulates its synthesis
c) it is broken down in conditions with high blood glucose levels
d) by degradation it provides blood glucose

A

c) it is broken down in conditions with high blood glucose levels

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140
Q

Which of the following statements about the influence of insulin on
blood glucose level is wrong:

a) Insulin reduces the level of blood glucose by accelerating its transport from
the blood into insulin-dependent tissues
b) Insulin stimulates the synthesis of liver and muscle glycogen
c) Insulin does not stimulate glucose transport in adipose tissue
d) Insulin stimulates glycolysis in the liver

A

c) Insulin does not stimulate glucose transport in adipose tissue

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141
Q

Which of the following enzymes is not present in the
muscles that could explain the fact that skeletal muscles
do not release blood glucose after the breakdown of
glycogen:
a) kinase of phosphorylase
b) phosphoglucomutase
c) glucose-6-phosphatase
d) glycogen phosphorylase

A

c) glucose-6-phosphatase

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142
Q

The following enzymes and hormones are involved in the cascade of
events leading to degradation of muscle glycogen under stress. Indicate
which of them does not participate:

a) Adrenaline
b) Adenylyl cyclase
c) Protein kinase A
d) Glucagon

A

a) Adrenaline

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143
Q

Which of the following hormones is a major regulator of blood glucose
level after meals:

a) glucagon
b) insulin
c) adrenaline
d) cortisol

A

b) insulin

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144
Q

Which of the following symptoms is not typical for patients with
diabetes:

a) glucosuria
b) ketoacidosis
c) hypoglycemia
d) polyuria

A

d) polyuria

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145
Q

The breakdown of liver glycogen is stimulated by glucagon via one of
the listed below secondary cell messengers. Which is that messenger?

a) calcium ions
b) cAMP
c) diacylglycerol
d) inositol-triphosphate

A

b) cAMP

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146
Q

Which of the following statements about the mechanism by which insulin
affects the activity of glycogen synthase (regulatory enzyme of
glycogenogenesis) is wrong:

a) insulin decreases the level of cAMP, which leads to dropout of the activation of Protein kinase A, catalyzing the formation of the active phosphorylated form of the protein, called “inhibitor-1”
b) When the inhibitory protein-1 is inactive (dephosphorylated) it does not inhibit the
activity of proteinphosphstase – 1
c) the active protein phosphatase-1 catalyzes the dephosphorylation of glycogen
synthase (glycogen synthase a)
d) insulin signaling leads to creating of the phosphorylated form of glycogen synthase
(glycogen synthase b)

A

a) insulin decreases the level of cAMP, which leads to dropout of the activation of Protein kinase A, catalyzing the formation of the active phosphorylated form of the protein, called “inhibitor-1”

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147
Q

Which of the following amino acids contains a hydroxyl group in its side
chain:

1) methionine
2) threonine
3) valine
4) serine

a) 1+2+3
b) 1+3
c) 2+4
d) 4

A

c) 2+4

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148
Q

Which of the following amino acids contains an aromatic ring in its side
chain:

1) isoleucine
2) proline
3) serine
4) tyrosine
a) 1+2+3
b) 1+3
c) 2+4
d) 4

A

d) 4

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149
Q
  • What is the electric charge of an amino acid in its isoelectric point:
    a)positive
    *b) zero
    *c) negative
    *d) -2
A

*b) zero

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150
Q
  • Which of the following amino acid residues in the protein molecules
    may participate in the formation of
  • ionic bonds:
    1) glutamate
  • 2) histidine
    3) arginine
    4) asparagine
  • a) 1+2+3
  • b) 1+3
    c) 2+4
    d) 1+2+3+4
A

a) 1+2+3

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151
Q
  • Which of the following values of the pH corresponds to the isoelectric
    point of the amino acid alanine, keeping in mind that pKa1 of the
    COOH group is 2.35 and pKa2 of the NH2 group is 9.69:
  • a) 4.8
    b) 7.24
    c) 6.02
    d) 3.0
A

c) 6.02

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152
Q

Which of the following amino acids has branched side chain:
* a) isoleucine
* b) tyrosine
c) serine
d) proline

A

a) isoleucine

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153
Q
  • Which of the following amino acids is basic:
    a) glutamate
  • b) arginine
  • c) methionine
  • d) alanine
A

b) arginine

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154
Q

Which of the following amino acids are essential:
* 1) valine
2) lysine
3) threonine
4) phenylalanine
* a) 1+2+3 b) 1+3
* c) 2+4
* d) 1+2+3+4

A
  • d) 1+2+3+4
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155
Q

Which chemical bonds participating in the building of protein
molecules are covalent:
* a) hydrogen
b) ionic
c) hydrophobic interactions
d) disulphide bond

A

d) disulphide bond

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156
Q

Which of the following biologically active peptides is / are tissue
hormone/s of gastrointestinal tract:
* 1) vasopressin
* 2) cholecystokinin
* 3) angiotensin
4) gastrin
* a) 1+2+3
* b) 1+3
c) 2+4
* d) 4

A

c) 2+4

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157
Q

Select the biologically active peptide which acts as a protector against
the harmful effect of reactive oxygen species (ROS):
* a) endorphin
* b) glutathione
* c) enkephalin
* d) melanocyte-stimulating hormone

A

b) glutathione

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158
Q

Which of the following amino acids is sulfur-containing:

a) isoleucine
b) tyrosine
c) serine
d) methionine

A

d) methionine

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159
Q

Which of the following biologically active peptides is
neuropeptide that binds to opioid receptors in the brain and appears
to be one of the natural pain relieving substances:
* a) endorphine
* b) glutathione
* c) neuropeptide Y
* d) melanocyte-stimulating hormone

A

a) endorphine

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160
Q

Which of the following statements about biologically active peptide
glutathione is wrong:
a) all peptide bonds in the glutathione are formed between –COOH
group bound to α-C atom of one of the amino acid and the -NH2
group of the next amino acid
* b) glutathione is a tripeptide
* c) sulfhydryl group of the cysteine residue has a major role in the
function of glutathione
* d) glutathione consists of glutamic acid, cysteine and glycine

A

a) all peptide bonds in the glutathione are formed between –COOH

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161
Q

Whichof the following biologically active peptides is a hormone with
powerful vasoconstrictor effect and is involved in the regulation of Na
ions in the body:
* a) cholecystokinin
* b) bradykinin
* c) melanocyte-stimulating hormone
* d) angiotensin II

A

d) angiotensin II

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162
Q

Select the chemical bonds involved in the formation of the secondary
structure of the protein molecules “β-sheet”:

  • a) intrachain and / or interchain hydrogen bonds between amino acid side radicals
  • b) intrachain and / or interchain hydrogen bonds between groups of the peptide bonds
  • c) ionic bond
  • d) disulphide bonds
A
  • b) intrachain and / or interchain hydrogen bonds between groups of the peptide bonds
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163
Q
  • Which of the following proteins do not belong to the group of
    metalloproteins:
  • a) transferrin
  • b) transcortin
  • c) ferritin
  • d) ceruloplasmin
A
  • b) transcortin
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164
Q

Which of the following plasma proteins does not perform transport function:

  • 1) α1-fetoprotein
  • 2) hemopexin
  • 3) C-reactive protein
  • 4) ceruloploasmin
    a) 1+2+3
  • b) 1+3
  • c) 2+4
  • d) 4
A
  • b) 1+3
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165
Q
  • Which of the following proteins is not structural:
  • a) casein
  • b) keratin
  • c) fibrillin
  • d) elastin
A
  • a) casein
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166
Q

Select the chemical bonds involved in the formation of the
secondary structure of the protein molecules “α-helix”:

a) interchain hydrogen bonds between amino acid side
radicals
b) ionic bonds
c) interchain hydrogen bonds between groups of the
peptide bonds
d) disulfide bridge

A

a) interchain hydrogen bonds between amino acid side
radicals

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167
Q
  • Which of the following proteins are not complex (proteides):

a) Lipoproteins
b) Albumin
c) Nucleoproteins
d) Hemoproteins

A

b) Albumin

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168
Q
  • Which is the non-protein component of the complex protein, casein:

a) Porphyrin structure
b) Phophoric acid
c) Nucleic acid
d) Lipid structure

A

d) Lipid structure

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169
Q

What type of biomolecules are the enzymes by their chemical nature:

  • a) nucleoproteins
  • b) lipoproteins
    c) glycolipids
    d) proteins
A

d) proteins

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170
Q

Which of the following statements about enzymes is wrong:

a) enzymes are biocatalysts
b) accelerate only thermodynamically possible reactions
c) withdraw the balance of the chemical reaction to produce
more product compared to the uncatalyzed reaction
d) they cause a decrease in the energy barrier of the chemical
reaction

A

d) they cause a decrease in the energy barrier of the chemical
reaction

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171
Q

Which of the compounds listed below is/are not cofactor/s of oxidoreductases?
1) NAD+
2)FAD*
3)lipoate
4)pyridoxal phosphate

a) 1+2+3

b) 1+3

c)2+4

d) 4

A

d) 4

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172
Q

Which of the following statements about the role of the metal ions in the enzymatic catalysis are true:
1) connecting with the apoenzyme they can stabilize the conformation of the active site
2)some of them participate in the electron transfer

3)by forming a complex with the substrate they can facilitate the binding to the active site
4)do not act as catalytic groups in the active site

a)1+2+3

b)1+3

c)2+4

d)1+2+3+4

A


a)1+2+3


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173
Q

What is the specific name of the enzymes which catalyze the transfer
of phosphate groups from ATP on substrates:

  • a) kinases
  • b) phosphatases
    c) oxidases
    d) dehydrogenases
A
  • a) kinases
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174
Q

To which of the following classes of the enzymes belong peptidases?
* a) hydrolases
* b) transferases
c) oxido-reductases
* d) isomerases

A

a) hydrolases

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175
Q

To which of the following classes of the enzymes belong
carboxylases?

a) hydrolases
b) ligases
c) Isomerases
d) Oxido-reductases

A

b) ligases

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176
Q

Which of the following statements about isoenzymes is wrong?
a)the isoenzyme forms of an enzyme are found in all individuals of the human population
b)the isoenzymes of a particular enzyme are localized in different subcellular structures, organs and tissues of one organism
C)the isoenzymes catalyze different chemical reactions
d)the isoenzymes differ in their physicochemical characteristics

A

C)the isoenzymes catalyze different chemical reactions

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177
Q

which type of reversible inhibitors of the enzymes may be referred antimetabolites:
a)competitive
b)non-competitive
c)uncompetitive
d)allosteric

A

a)competitive

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178
Q

Which of the following statements about the substances modulating the catalytic activity of allosteric enzymes is wrong:

a)modulators might be metabolites of the pathway in which acts the allosteric enzyme or metabolites of other metabolic pathways

b)the final product of the pathway that results in excessive concentrations is often an inhibitor of the regulatory allosteric enzyme of the same pathway

c)the action of the metabolites as modulators depends on their concentration in the cell

d)when the substrate of the metabolic pathway is in excess it always acts as an activator of the allosteric regulatory enzyme in the same pathway

A

d)when the substrate of the metabolic pathway is in excess it always acts as an activator of the allosteric regulatory enzyme in the same pathway

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179
Q

Which of the following effects on the enzymes is considered to be irreversible inhibition:
1. permanent binding and blocking of the functional group in the active site
2. destroying the native structure of the enzyme under the action of chemical agents
3. permanent binding and blocking the enzyme cofactor
4. binding with the active center by structural analogy with the substrate
a) 1+2+3
b) 1+3
c)2+4
d)1+2+3+4

A

b) 1+3

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180
Q

Which of the following statements about the impact of the catalytic activity of regulatory enzymes by covalent modification (phosphorylation / dephosphorylation) is wrong:
a) phosphorylation represents binding by covalent bond of the phosphate group, donor of which is ATP, to a specific functional group of an amino acid residue of the apoenzyme
b)the functional group which binds the phosphate group from ATP is an amino group, not involved in the formation of the peptide bond
c) phosphorylation is catalyzed by protein kinases
d)in dephosphorylation which is catalyzed by protein phosphatases, the covalent bond between the phosphate group and a functional group of apoenzyme is hydrolyzed while giving inorganic phosphate

A

b)the functional group which binds the phosphate group from ATP is an amino group, not involved in the formation of the peptide bond

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181
Q

Which of the following statements about alloenzymes is wrong:
a) many of the enzymes have alloenzyme forms
b)alloenzymes are encoded by different alleles of the same gene
c)most of the alloenzymes differ by one or several amino acid residues
d)each individual of the human population has several forms of a alloenzymes of an enzyme

A

d)each individual of the human population has several forms of a alloenzymes of an enzyme

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182
Q

Bearing in mind that organophosphate compounds (e.g. the chemical weapons - sarin, soman, tabun) are irreversible inhibitors of enzymes, indicate which of the following amino acid functional groups in the active site of the enzymes are blocked by covalent bonds by those enzyme toxins:
a)carboxyl group of glutamate
b)ammo group of lyrine
c)hydroxyl group of serine
d)sulfhydryl group of cysteine

A

c)hydroxyl group of serine

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183
Q

Which of the enzymes are studied in the diagnosis of liver diseases (e.g. viral hepatitis, obstructive jaundice etc)
1. Acidic phosphatase
2. AsAT (GOT)
3. Creatine kinase
4) ALAT (GPT)

a) 1+2+3

b) 1+3

c) 2+4

d) 1+2+3+4

A


c) 2+4

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184
Q

Tetrahydrofolate is a co-factor of transferases which catalyze the transfer of some of the listed below functional groups. Which are those groups?
a)one-carbon groups
b)amino groups
c)phosphate groups
d)reducing equivalints (H2)

A

a)one-carbon groups

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185
Q

Which of the enzymes are studied in the diagnosis of myocardial infarction:
1. AsAT (GOT) - aspartate aminotransferase
2. LDH - lactate dehydrogenase
3. CK - creatine kinase
4)HBDH - alpha-hydroxybutyrate dehydrogenase
a) 1+2+3
b)1+3
c)2+4
d) 1+2+3+4

A

d) 1+2+3+4

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186
Q

Which of the following statements about allosteric enzymes is wrong?
A)generally they are oligomeric proteins, i.e. they have quaternary structure
b) the substrate is always allosteric activator
c)contain one or more allosteric sites which bind the modulator/modulators
d)the binding of the modulator is reversible

A

b) the substrate is always allosteric activator

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187
Q

Enzymes of which group catalyse synthetic
reactions requiring energy most often supplied by
ATP:

a) Ligases
b)Oxido-reductase
c) Isomerases
d)lyases

A

a) Ligases

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188
Q

Which of the following diseases, caused by enzyme deficiency, are deposition
diseases?

1) glycogenosis
2) tyrosinosis 3) sphingolipidoses
4) porphyrias
a) 1+2+3
b) 1+3
c) 2+4
d) 1+2+3+4

A

b) 1+3

189
Q

The symptoms of which of the following enzymopathies are due to
acceleration of the minor pathways of the substrates of the main
metabolic pathway having enzyme deficiency:

a) fructosuria
b) gout
c) phenylketonuria
d) porphyria

A

b) gout

190
Q

The deficiency of which of the following vitamins causes the disease
“beriberi”?

  • a) folic acid
  • b) thiamine
  • c) biotin
  • d) ascorbic acid
A

b) thiamine

191
Q

The deficiency of which of the following vitamins causes the disease
scurvy?

  1. ascorbic acid
  2. thiamine
  3. Biotin
  4. niacin
A
  1. ascorbic acid
192
Q

Which of the following vitamins is not water soluble:
a) Riboflavin
b) Cholecalciferol
c) Biotin
d) Niacin

A

b) Cholecalciferol

193
Q

Which of the following statements about vitamin b6 is wrong:

a) It exist in three natural derivatives: pyroxine (ol), pyridoxal,
pyridoxamine.
b) Biologically active are two of the phosophates of the two forms, as
pyridoxalphosphate is main co-factor form.
c) Pyridoxalphosphate is cofactor only of transaminases
d) Pyridoxalphophate stabilizes and is required for activation of muscle
glycogen phosphorylase

A

c) Pyridoxalphosphate is cofactor only of transaminases

194
Q

Which of the following enzyme groups biotin (vitamin h.) is a prosthetic
group?

a) Transaminases
b) Dehydrogenases
c) Decarboxylases
d) carboxylases

A

b) Dehydrogenases

195
Q

Which of the following types of lipids is not a component of the
membrane structures:

  • a) cholesterol
  • b) triacylglycerols
    c) cardiolipins
    d) phosphatidylethanolamine
A

b) triacylglycerols

196
Q

Which of the following lipids are glycolipids:

  • 1) sphingomyelins
    2) gangliosides
    3) cephaline
  • 4) cerebrosides a) 1+2+3
  • b) 1+3
  • c) 2+4
  • d) none of the above mentioned
A
  • d) none of the above mentioned
197
Q

Which of the following statements about the activation of fatty acids
before their inclusion in β- oxidation is wrong:

  • a) activation of fatty acids is by binding their carboxyl group with coenzyme A
    and turning
  • them into acyl CoA derivatives
  • b) activation of the fatty acids takes place in the mitochondrial matrix
  • c) activation of the fatty acids takes place in the endoplasmic reticulum
  • d) long chain fatty acids are activated
A

c) activation of the fatty acids takes place in the endoplasmic reticulum

198
Q

Which of the following pairs of vitamins act as coenzymes in the β-
oxidation of fatty acids with an odd number of carbon atoms:

  • a) vit. B1 and folic acid
  • b) biotin and vit. B12
  • c) folic acid and biotin
  • d) vit.В12 and vit.В1
A

b) biotin and vit. B12

199
Q
  • Which of the following shuttle mechanisms is involved in the transfer
    of activated fatty acids from the cytosol into the mitochondria?:
  • a) malate-aspartate
  • b) glycerol-phosphate
  • c) acyl-carnitine
  • d) none of the above mentioned
A
  • c) acyl-carnitine
200
Q

Which of the following metabolites is an allosteric inhibitor of the
regulatory enzyme of β- oxidation:

  • a) Propionyl-CoA
  • b) Malonil-CоА
  • c) Butyryl-CoA
  • d) none of the above mentioned
A
  • b) Malonil-CоА
201
Q

Which of the following statements about ketone bodies is wrong:

  • a) substrate for the synthesis of ketone bodies is acetyl CoA, obtained from
    the oxidative decarboxylation of pyruvate
  • b) ketone bodies are acetoacetate, β-hydroxybutyrate and acetone, as
    acetone is product of acetoacetate degradation.
  • c) ketone bodies are an energy source alternative of glucose
  • d) the concentration of the β-hydroxybutyrate in the blood is usually higher
    than that of the acetoacetate
A
  • d) the concentration of the β-hydroxybutyrate in the blood is usually higher
    than that of the acetoacetate
202
Q

In which of the following organs the synthesis of ketone bodies
(ketogenesis) takes place:

  • a) skeletal muscles
  • b) brain
  • c) kidneys
  • d) liver
A
  • d) liver
203
Q

Which of the following hormones stimulates ketogenesis in the
periods of fasting:

  • a) insulin
  • b) cortisol
  • c) glucagon
  • d) none of the above mentioned
A
  • c) glucagon
204
Q
  • Triacylglycerols from the diet are transported by one of the following
    transport form. Which is that:
  • a) chylomicrons
  • b) verylow-densitylipoproteins(VLDL)
  • c) high-density lipoproteins (HDL)
  • d) low-densitylipoproteins(LDL
A
  • a) chylomicrons
205
Q

Which of the following enzymes catalyzes the hydrolysis of
triacylglycerols located in different lipoprotein complexes (e.g. in
chylomicrons, VLDL)

  • a) lecithin-cholesterol-acyltransferase
  • b) lipoproteinlipase
  • c) pancreatic lipase
  • d) hormone-sensitive lipase
A
  • b) lipoproteinlipase
206
Q

Which of the following transport forms of lipids contain the so-called,
alpha (α) cholesterol, which usually is determined in clinical
laboratory tests of the blood.
* a) chylomicrons
* b) low-density lipoproteins(LDL)
* c) high-density lipoproteins (HDL)
* d) very low-density lipoproteins(VLDL

A
  • c) high-density lipoproteins (HDL)
207
Q

Which of the following enzymes catalyzes the hydrolysis of
triacylglycerols located in different lipoprotein complexes (e.g. in
chylomicrons, VLDL)

  • a) lecithin-cholesterol-acyltransferase
  • b) lipoproteinlipase
  • c) pancreatic lipase
  • d) hormone-sensitive lipase
A
  • b) lipoproteinlipase
208
Q

Which of the following statements for the synthesis of saturated fatty
acids with an even number of carbon atoms (palmitic acid) is false:

  • a) direct substrate for the synthesis is malonyl-CoA
  • b) NAD.H serves as a donor of reducing equivalents
  • c) synthesis takes place in the cytosol
  • d) binding of each of the two-carbon fragment in the elongation
    process of the carbon chain of the fatty acid is performed in four
    metabolic step
A
  • d) binding of each of the two-carbon fragment in the elongation
    process of the carbon chain of the fatty acid is performed in four
    metabolic step
209
Q

Which of the following enzymes involved in β-oxidation of fatty
acids with an even number of carbon atoms, is a regulatory enzyme
of the process:

  • a) carnitine acyltransferase I (carnitine:palmitoyltransferase I)
  • b) acyl CoA dehydrogenase
  • c) enoyl CoA hydrogenase
  • d) carnitineacyltransferaseII(carnitine:palmitoyltr
A
  • a) carnitine acyltransferase I (carnitine:palmitoyltransferase I)
210
Q
  • Which of the following statements about the regulation of the activity
    of the regulatory enzyme of fatty acid biosynthesis, acetyl-CoA
    carboxylase is false:
  • a) the activity is regulated by the mechanism of covalent modification
    (phosphorylation / dephosphorylation), аs the active form is phosphorylated.
  • b) the activity is influenced by the action of hormones, as insulin stimulates
    the enzymatic activity
  • c) the activity is regulated by the mechanism of covalent modification
    (phosphorylation / dephosphorylation), the active form is dephosphorylated.
  • d) the activity of the enzyme is regulated allosterica
A
  • c) the activity is regulated by the mechanism of covalent modification
    (phosphorylation / dephosphorylation), the active form is dephosphorylated.
211
Q

Which one of the metabolites of glycolysis occurring in adipocytes, is
converted to glycerol-3- phosphate being one of the substrates for
the synthesis of triacylglycerols in adipose tissue:

  • a) glyceraldehyde-3-phosphate
    b) pyruvate
  • c) 3-phosphoglycerate
  • d) dihydroxyacetonephosphate
A
  • d) dihydroxyacetonephosphate
212
Q

Which of the following enzymes is regulatory in degradation of
triacylglycerols in adipose tissue:

  • a) lipoprotein lipase
  • b) glycerolkinase
  • c) phospholipase
  • d) hormone-sensitive lipase
A
  • d) hormone-sensitive lipase
213
Q

Which of the following statements about the degradation of
triacylglycerols in adipose tissue is false:

a)triacylglycerols are degraded when the insulin/glucagon ratio in the blood is high
b)triacylglycerols are degraded during fasting
*c) triacylglycerols are degraded rapidly in patients with diabetes mellitus
* d) triacylglycerols are degraded under elevated level

A

a)triacylglycerols are degraded when the insulin/glucagon ratio in the blood is high

214
Q
  • Which of the following biological functions of cholesterol is not
    correct:
  • a) cholesterol participates in the construction of the cell membranes as a
    stabilizing component
  • b) cholesterol serves as a precursor for steroid hormone synthesis
  • c) cholesterol serves as a precursor for vitamin E synthesis
  • d) cholesterol serves as a precursor for bile acids synthesis
A
  • c) cholesterol serves as a precursor for vitamin E synthesis
215
Q
  • Which of the following metabolites is obtained in the biosynthesis of
    ketone bodies, and in the biosynthesis of cholesterol in the liver, i.e.,
    appears to be a key metabolite.
  • a) mevalonic acid
  • b) hydroxy-methylglutaryl-CoA
  • c) ß- hydroxybutyrate
  • d) isopentenylpyrophosphate
A
  • b) hydroxy-methylglutaryl-CoA
216
Q

Which of the following cofactors supplies reducing equivalents for the
action of the enzyme HMG-CoA reductase:
* a) NAD.H
b) FAD.Н2
c) NADP.Н
* d) FMN.H2

A
  • a) NAD.H
217
Q

Which of the following statements about regulation of cholesterol
biosynthesis is true:

  • a) cholesterol synthesis is not affected by the concentration of cholesterol
  • b) cholesterol acts as an allosteric activator of the HMG-CoA reductase
  • c) cholesterol acts as an allosteric inhibitor of HMG-CoA synthase
  • d) cholesterol represses the synthesis of HMG-CoA reductase
A
  • d) cholesterol represses the synthesis of HMG-CoA reductase
218
Q

Which of the following statements about the regulation of enzyme
activity of 7α-hydroxylase which regulates the conversion of
cholesterol to bile acids in the liver is false:

  • a) the catalytic activity of 7α-hydroxylase is regulated by phosphorylation /
  • dephosphorylation, and the active form of the enzyme is dephosphorylated
  • b) cholesterolenhances7α-hydroxylasemRNA
  • c) bile acids inhibit the enzyme synthesis
  • d) in Vit. C deficiency the metabolic step catalyzed by 7α-hydroxylase slows
    down.
A
  • a) the catalytic activity of 7α-hydroxylase is regulated by phosphorylation /
  • dephosphorylation, and the active form of the enzyme is dephosphorylated
219
Q
  • Which of the following statements about arachidonic acid is wrong:
    *
  • A) arachidonic acid is a polyunsaturated FA containing 20 carbon atoms
  • B) arachidonic acid is 3 polyunsaturated fatty acid
  • C) arachidonic acid is a precursor for the synthesis of eicosanoids:
    prostaglandins, thromboxanes with 2 double bonds and leukotrienes with 4
    double bonds
  • D) arachidonic acid participates in the construction of membrane
    phospholipids
A
  • B) arachidonic acid is 3 polyunsaturated fatty acid
220
Q

Which of the following statements about the physiological functions
of eicosanoids is false:

  • a) They participate in inflammatory processes, in injuries and
    infections
  • b) Some of the eicosanoids are involved in platelet aggregation
  • c) Some regulate smooth muscle contractions (intestine, uterus)
  • d) All eicosanoids act as vasoconstrictors
A
  • d) All eicosanoids act as vasoconstrictors
221
Q
  • The high concentration of which of the lipid transport forms listed
    below decreases the risk of developing of atherosclerosis and
    coronary heart disease?
  • a) HDL
  • b) chylomicrons
  • c) LDL
    d) VLDL
A
  • a) HDL
222
Q

Which of the listed subcellular compartments is the place, where the
oxidation of fatty acids leading to introduction of double bond is
performed:

  • a) mitochondria
  • b) lysosomes
  • c) endoplasmic reticulum
  • d) cytoplasm
A
  • c) endoplasmic reticulum
223
Q
  • Eicosatetraenoic acid is a precursor for the synthesis of:
  • 1) prostanoids with 2 double bonds
    2) leukotrienes with 3 double bonds
    3) lipoxins with 4 double bonds
  • 4) prostanoids with 3 double bonds
  • a) 1+2+3
    b) 1+3
    c) 2+4
  • d) none
A

c) 2+4

224
Q
  • The oxidative phase of the PPP (pentose phosphate pathway) is important
    for:
  • 1) cholesterol synthesis
  • 2) synthesis of ATP
    3) fatty acid synthesis
  • 4) gluconeogenesis
  • a) 1+2+3
  • b) 1+3
  • c) 2+4
  • d) allfour
A
  • c) 2+4
225
Q
  • Which of the following mechanisms, for activating of the
    biosynthesis of fatty acids from the insulin is incorrect:
  • a) insulin with its signaling cascade leads to the active
    unphosphorylated form of the regulatory enzyme acetyl-CoA
    carboxylase
  • b) insulin with its signaling cascade leads to induction of the
    biosynthesis of the regulatory enzyme of fatty acid synthesis - acetyl- CoA carboxylase
  • c) insulin with its signaling cascade leads to induction of the
    biosynthesis of the multifunctional enzyme complex, fatty acid synthase
    complex
  • d) insulin with its signaling cascade leads to activation of the enzyme
    glycerol-3- phosphate acyl transferase, via maintaining of its
    unphosphorilated form
A
  • d) insulin with its signaling cascade leads to activation of the enzyme
    glycerol-3- phosphate acyl transferase, via maintaining of its
    unphosphorilated form
226
Q

Which of the following compounds are cholesterol derivatives?

1) aldosterone
2) adrenaline
3) cortisol
4) cholicacid
a) 1+2+3
b) 1+3
c) 3+4
d) 1+3+4

A

a) 1+2+3

227
Q

Which of the following compounds is a key (a key metabolite) in the
synthesis of most glycerolipids?

а) choline
b) CDP-choline
c) phosphatidic acid
d) CDP- diacylglycerol

A

c) phosphatidic acid

228
Q

Which of the enzymes that catalyze reactions in the synthesis of
glycerolipids is regulatory?

a) phosphatidic acid phosphatase
b) glycerol-3P-acyltransferase
c) diacylglycerol acyltransferase
d) phosphatidylinositol synthase

A

b) glycerol-3P-acyltransferase

229
Q

Which of the following groups of lipids are glycolipids?

1) sphingomyelins
2) gangliosides
3) cerebrosides
4) lecithins
a) 1+2+3
b) 2+3
c) 1+4
d) 2+3+4

A

d) 2+3+4

230
Q

Which of the following essential polyunsaturated fatty acids (PUFA) are
supplied only from foods of animal origin.

1) linoleicacid
2) arachidonicacid
3) eicosapentaenoic acid
4) linolenic acid
a) 1+2+3
b) 2+3
c) 1+4
d) 2+3+4

A

b) 2+3

231
Q

On which positions in the hydrocarbon chains of the fatty acids double
bonds may be introduced in man (desaturases function in human
cells)?

а) 4, 5, 8 and 9
b) 4, 5, 6 and 9
c) 5, 8, 11 and 14
d) 4, 5, 8 and 9

A

d) 4, 5, 8 and 9

232
Q

Which of the following biological effects are typical for PGE2?

  • 1) bronchoconstrictor
  • 2) vasodilator
  • 3) inhibits the secretion of gastric juice
  • 4) inhibits the uterine contractions
  • a) 1+2+3
  • b) 2+3
    c) 2+4
    d) 2+3+4
A

c) 2+4

233
Q
  • Which of the following reactions and processes provide reducing
    equivalents (NADPH) used in the synthesis of fatty acids?
  • 1) anaerobic glycolysis
    2) pentose phosphate pathway
    3) reaction catalyzed by malate dehydrogenase
  • 4) reaction catalyzed by “malate” enzyme
  • a) 1+2+3
  • b) 2+3
    c) 2+4
  • d) 2+3+4
A

c) 2+4

234
Q
  • Which of the following compounds is the direct donor of 14 of the 16
    carbon atoms in the synthesis of palmitic acid?
  • а) acetyl-CоА
    b) acyl-CоА
    c) malonyl-CоА
    d) methilmalonyl-CоА
A

c) malonyl-CоА

235
Q

Which of the following compounds are not allosteric activators of the main
key enzyme in the synthesis of fatty acids, Acetyl CoA carboxylase?

1) acyl-CоА
2) acetyl-CоА
3) malonyl-CоА
4) citrate
a) 1+2+3
b) 2+3
c) 2+4
d) 2+3+4

A

c) 2+4

236
Q

In which of the following organs the synthesis of ketone bodies
(ketogenesis):takes place
a) skeletal muscle
b) brain
c) heart muscle
d) liver

A

d) liver

237
Q

Which of the following hormones stimulates ketogenesis in periods of
fasting?

a) insulin
b) cortisol
c) ACTH
d) glucagon

A

d) glucagon

238
Q

Which of the following compounds are ketone bodies with metabolic
importance for tissues:

  • 1) acetoacetate
    2) oxaloacetate
    3) β- hydroxybutyrate
  • 4) acetone
  • a) 1+2+3
  • b) 1+3
  • c) 2+3
  • d) 1+3+4
A
  • a) 1+2+3
239
Q

Which of the following lipoprotein complexes are the main carriers of TAG to
peripheral tissues:

1) Chylomicrons
2) VLDL
3) LDL
4) HDL
a) 1+2+3
b) 1+2
c) 1+3+4
d) 3+4

A

b) 1+2

240
Q

Which of the following enzymes play an important role in the metabolism
of lipoprotein complexes:

  • 1) hepaticlipase
  • 2) pancreaticlipase
  • 3) lipoprotein lipase
  • 4) LCAT (lecithin cholesterol acyltransferase)
  • a) 1+2+3
  • b) 1+2
  • c) 1+3+4
  • d) 3+4
A
  • d) 3+4
241
Q

Which of the following lipoprotein complexes transport the “bad”
cholesterol and raising of their levels is a risk factor for
atherosclerosis:

  • а) chylomicrons
  • b) VLDL
    c) LDL
    d) HDL
A

c) LDL

242
Q

Which of the following coenzymes serves as a donor of reducing
equivalents in the synthesis of fatty acids in fatty acid synthase
complex?

  • a) NAD.Н
  • b) FAD.Н2
  • c) NADP.Н
  • d) FMN.Н2
A
  • c) NADP.Н
243
Q

How many turns (cycles) of the spiral of β-oxidation occur for
oxidation of palmitic acid (Palmitoyl-CoA) to Acetyl-CoA?

  • a) 10
  • b) 8
  • c) 7
  • d) 6
A
  • c) 7
244
Q

In which of the following cell compartments of hepatocytes the
ketogenesis occurs?
*
* a) cytosol
* b) mitochondria
* c) endoplasmic reticulum
* d) lysosomes

A
  • b) mitochondria
245
Q

Which of the following metabolites is a product of the
degradation of ketone bodies (ketolysis) in extrahepatic tissues?

  • a) malonyl -CоА
  • b) acetyl-CоА
  • c) succinyl -CоА
  • d) propionyl-CoA
A
  • b) acetyl-CоА
246
Q

The catabolic pathways are primarily:
Reductive and endergonic
Endergonic and exergonic
Oxidative and endergonic
Oxidative and reductive
Oxidative and exergonic

A

Oxidative and exergonic

247
Q

Insulin synthesis: 1) occurs in the β-cells of the Langerhans islands, 2) is initiated at a low blood glucose, 3) occurs in the mitochondria and Golgi apparatus, 4) occurs with the release of C-peptide, 5) it is composed of 3 polypeptide chains connected by 2 disulfide bridges
1 + 4
3 + 5
2 + 5
1 + 2
2 + 3

A

1 + 4

248
Q

Which of the following enzymes is NOT tested for myocardial infarction?
ALT (GPT)
creatine kinase
lactate dehydrogenase
alpha-hydroxybutyrate dehydrogenase
AST (GOT)

A

ALT (GPT)

249
Q

Which of the listed statements are correct? 1) pyruvate is the substrate for the synthesis of ketone bodies 2) a significant increase in the concentration of ketone bodies leads to a condition called ketoacidosis 3) ketone bodies are an alternative source of energy for the extrahepatic tissues (muscles, brain) 4) ketone bodies are the main energy source for the liver 5) after activation ketone bodies enter the glycolysis, where they are completely oxidized
3+4
1+3
2+5
2+3
1+5

A

2+3

250
Q

Which of the enzymes that catalyze reactions in the synthesis of
glycerolipids is regulatory?

a) phosphatidic acid phosphatase
b) glycerol-3P-acyltransferase
c) diacylglycerol acyltransferase
d) phosphatidylinositol synthase

A

b) glycerol-3P-acyltransferase

251
Q

In the cells, the activated fatty acids are transported through the inner mitochondrial membrane into the matrix with the help of:
carnitine
carnosine
carotene
creatine
xanthine

A

carnitine

252
Q

Which of the following enzymes is a component of the glycerol phosphate shuttle?
malate dehydrogenase
triose phosphate isomerase
glycerol kinase
glycerol 3-phosphate dehydrogenase
glyceraldehyde 3-phosphate dehydrogenase

A

glycerol 3-phosphate dehydrogenase

253
Q

Cofactor of galactokinase is:
NADH
NADPH
FMN
ATP
FAD

A

ATP

254
Q

An example of a functional plasma enzyme is:
creatine kinase
aspartate aminotransferase
α-amylase
lactate dehydrogenase
ceruloplasmin

A

α-amylase

255
Q

Which are the enzymes that deliver NADPH for the synthesis of fatty acids and cholesterol? 1) α-ketoglutarate dehydrogenase 2) malic enzyme 3) the cytosolic isocitrate dehydrogenase 4) the mitochondrial isocitrate dehydrogenase 5) glucose-6-phosphate dehydrogenase
1+3+4
1+3+5
1+2+3
2+3+4
2+3+5

A

2+3+5

256
Q

Which of the following are the regulatory enzymes of glycolysis?
1) hexokinase
2) 2) glyceraldehyde 3-phoshate dehydrogenase
3) triose phosphate isomerase
4) phosphofructokinase I
5) pyruvate kinase
2+4+5
1+2+3
1+4+5
2+3+4

A

1+4+5

257
Q

Which of the listed factors are needed for activation of pancreatic lipase: 1) acidic conditions 2) chloride ions 3) neutral or weak alkaline conditions 4) bile acids and lysolecithins 5) the action of colipase
2+3+5
1+2+5
1+2+3
3+4+5
1+3+4

A

3+4+5

258
Q

Disulfide bonds in the protein molecules are formed between:
two methionine residues
two cysteine residues
two serine residues
two glutamine residues

A

two cysteine residues

259
Q

Collagen is characterized by the presence of: 1) hydroxyprolyl and hydroxylysyl amino acid residues 2) hydroxyprolyl, but not hydroxylysyl amino acid residues 3) carbohydrate component 4) a structure called “desmosine” 5) triple-helical structure
2+3+5
1+3+4
1+3+5
1+2+3
2+3+4

A

1+3+5

260
Q

Which of following statements are true?
1) Macroergic compounds are a link between exergonic and endergonic processes
2) ATP contains three macroergic bonds
3) ATP contains two macroergic bonds
4) ADP contains two macroergic bonds 5) AMP contains only one macroergic bond
1+2
2+5
1+5
1+3
1+4

A

1+3

261
Q

Sphingosine is a precursor of: 1) lecithins 2) phosphatidylinositols 3) cerebrosides 4) gangliosides 5) sphingomyelins
1+3+5
3+4+5
1+3+4
2+4+5
1+2+5

A

3+4+5

262
Q

Which of the following proteins is an iron-storing protein?
hephaestin
hemosiderin
transferrin
ferritin
ceruloplasmin

A

ferritin

263
Q

Which of the following statements regarding the β-oxidation of fatty acids with an even number of C-atoms are correct?
1) the oxidation of fatty acids is a mitochondrial process
2)the oxidation of fatty acids is an anaerobic process
3)the end products are Acetyl-CoA, malonyl-CoA, NADH and FADH2
4) the end products are Acetyl-CoA, propionyl-CoA, NADH and FADH2
5) the end products are Acetyl-CoA, NADH and FADH2
1+5
2+5
2+4
3+4
1+3

A

1+5

264
Q

Which of the listed molecules are oxidized in the Krebs cycle? 1) non-essential amino acids (the carbon skeleton) 2) ketone bodies 3) acetyl-CoA derived from the pyruvate dehydrogenase complex 4) propionyl-CoA obtained by the degradation of fatty acids with an odd number of carbon atoms 5) the final products of the β-oxidation
2+4+5
all of them
1+3+4
1+3+5
2+3+5

A

1+3+5

265
Q

Which of the following enzymes are expressed only in the liver? 1) urease 2) 3-hydroxy-3-methyl-glutaryl-CoA reductase 3) carbamoyl phosphate synthetase I 4) pyruvate carboxylase 5) bilirubin UDP-glucuronyl transferase activity
4+5
2+4
3+5
1+3
1+5

A

4+5

266
Q

Protein denaturation leads to: 1) Changes of amino acid composition of the protein molecule 2) Destroying primary structure of the protein molecule 3) Loss the biological activity of the protein 4) Increasing the chemical reactivity of the polypeptide chain of the protein 5) Destroying the secondary, tertiary and quaternary structure
2+3+4
2+3+5
3+4+5
1+3+4
1+2+3

A

3+4+5

267
Q

The process of heat production depends on:
1) the activity of mitochondrial respiratory chains when the electron transport and phosphorylation are uncoupled
2) the short electron transport chains localized in the endoplasmic reticulum
3) the activity of lysosomal short electron transport chains
4) ion channels in the inner mitochondrial membrane when open
5) ion channels in the inner and outer mitochondrial membranes when open
1+5
2+3
3+5
2+5
1+4

A

1+4

268
Q

Carbamoyl phosphate synthetase I, which catalyses the formation of carbamoyl phosphate in the urea cycle: 1) is located in the mitochondria of hepatocytes 2) is located in the cytoplasm of hepatocytes 3) is a regulatory enzyme 4) is allosterically activated by N-acetylglutamate 5) is allosterically activated by N-acetylglutamine
2+3+5
3+4+5
2+3+4
1+3+5
1+3+4

A

1+3+5

269
Q

Antithrombin III: 1) participates in fibrinolysis 2) inhibits the activity of enzymes of the blood clotting process 3) is activated by urokinase 4) works in a complex with the tissue factor (factor III) 5) is activated by heparin
2+4
3+4
2+5
4+5
1+3

A

2+5

270
Q

Which of the following enzymes catalyse reactions from pentose phosphate pathway?
phospho hexose isomerase
2) glucose 6-phosphate dehydrogenase
3) transaldolase
4) transketolase
5) hexokinase
1+3+4
2+3+5
3+4+5
1+2+5
2+3+4

A

2+3+4

271
Q

Which of the following enzymes of purine biosynthesis are allosterically regulated? 1) phosphoribosyl pyrophosphate (PRPP) synthetase 2) formyl transferase 3) glutamine-PRPP amidotransferase 4) adenylosuccinase 5) xanthine oxidase
3+4
2+5
1+3
2+4
1+5

A

1+5

272
Q

Hemorrhages in the joints and subcutaneous tissue, formation of ulcers that are difficult to heal, softening of the gums, anemia are clinical signs of the disease:
pellagra
pernicious anemia
scurvy
beriberi
gout

A

scurvy

273
Q

Which of the following enzymes catalyze the irreversible steps in gluconeogenesis? 1) aldolase 2) glucose 6-phosphatase 3) fructose 1,6-bisphosphatase 4) pyruvate kinase 5) pyruvate carboxylase
2+3+4
1+2+3
2+3+5
3+4+5
1+3+5

A

2+3+5

274
Q

The role of free fatty acids in the process of heat production in brown adipose tissue is: 1) isolating the internal organs of the low temperature of the environment 2) when oxidized, they supply hydrogen to the respiratory chain 3) synthesis of triacylglycerols 4) synthesis of ketone bodies 5) activate the uncoupling protein 1.
1+2
3+5
2+4
1+3
2+5

A

2+5

275
Q

How many are the ATP molecules synthesized by the short electron transport chains during the process of microsomal oxidation?
no ATP molecules
two ATP molecules
one ATP molecule
three ATP molecules
four ATP molecules

A

two ATP molecules

276
Q

In transamination: 1) amino acids are converted to biogenic amines 2) one amino acid is converted to a keto acid and another keto acid is converted to the corresponding amino acid 3) the amino groups of amino acids are released as free ammonia 4) pyridoxal phosphate participates as a cofactor 5) tetrahydrobiopterin participates as a cofactor
2+5
1+3
2+4
3+4
1+5

A

2+4

277
Q

In which part of the cell does the pentose phosphate pathway takes place?
the cytosol
the cytosol and matrix of the mitochondria
the inner membrane of the mitochondria
the mitochondrial matrix
peroxisomes

A

the cytosol

278
Q

Cori’s cycle is about:
synthesis of glutamine in the brain and its deamination in the liver
synthesis of urea in the liver and its excretion with urine
binding of aspartate to a metabolite and further cleavage of its carbon skeleton in the form of fumarate
formation of alanine from pyruvate in the muscles and formation of glucose from alanine in the liver
formation of lactate from glucose in the skeletal muscles and formation of glucose from lactate in the liver

A

formation of lactate from glucose in the skeletal muscles and formation of glucose from lactate in the live

279
Q

Which of the following hormones are recognized and bound by intracellular receptors? 1) retinoic acid 2) triiodothyronine (T3) 3) TSH 4) calcitriol 5) serotonin
2+3+4
1+3+5
1+2+4
1+2+3
2+3+5

A

1+2+4

280
Q

Which of the listed enzymes is an enzyme complex of the respiratory chain which does NOT pump protons into the intermembrane space?
Cyt.C: oxygen oxidoreductase
Cytochrome reductase
Succinate dehydrogenase
NAD.H: ubiquinone oxidoreductase
Isocitrate dehydrogenase

A

Succinate dehydrogenase

281
Q

Which is the mechanism involved in the regulation of the enzymes of Krebs cycle?
a)allosteric control, exerted by either the substrates or products of the chemical reactions
b)proteolytic “maturation” of the protein structure of the enzymes
c)reversible covalent modifications, caused by hormonal signal cascades
d)with the aid of additional enzymes called dprotein kinases or phosphatases
changes in the intracellular location of the enzymes

A

a)allosteric control, exerted by either the substrates or products of the chemical reactions

282
Q

Which of the end products of heme degradation are increased in parenchymal jaundice (hepatitis)? 1) urobilinogen in urine 2) bilirubin in the urine 3) indirect serum bilirubin 4) direct serum bilirubin 5) stercobillin in the stool
2+3+4
1+3+4
2+3+5
1+2+3
1+3+5

A

2+3+4

282
Q

Which of the following reactions are reactions of the covalent modification of regulatory enzymes:
1)acetylation
2) methylation
3) phosphorylation
4) adenylation
5) uridinylation
1+3+5
2+4+5
1+2+3
all of them
1+3+4

A

1+2+3

283
Q

Which statements about hormone-sensitive lipase are correct? 1) it is activated by insulin 2) the active form is the dephosphorylated 3) it is activated by glucagon 4) the active form is the phosphorylated 5) it hydrolyses monoacylglycerols to form free fatty acids (FFAs) and glycerol
1+5
1+3
1+2
2+4
3+4

A

1+5

284
Q

Which of the listed compounds are known as ketone bodies? 1) oxaloacetate 2) acetone 3) acetoacetate 4) 3-hydroxybutirate 5) acetoacetyl-CoA
3+4+5
1+3+5
1+2+3
1+2+5
2+3+4

A

2+3+4

285
Q

Which of following statements about non-competitive inhibitors are true? 1) Inhibitor is not a structural analog of the substrate 2) Inhibitor is a structural analogue of the substrate 3) Binds to groups from the active center of the enzyme 4) Binds to groups outside the active site of the enzyme 5) The inhibitory effect depends only on the concentration of the inhibitor
2+3+4
1+3+4
2+3+5
1+3+5
1+4+5

A

1+4+5

286
Q

Respiratory chains: 1) are located in the outer mitochondrial membrane 2) are located in the inner mitochondrial membrane 3) are complex structures, assembled from enzymes, non-enzyme proteins and redox-systems (electron carriers) 4) transfer hydrogen from NADH or other substrates to oxygen as a final acceptor 5) could act under both aerobic and anaerobic conditions
1+3+4
2+3+4
1+3+5
1+4+5
2+4+5

A

2+3+4

287
Q

Which of the following is NOT typical for adipocytes of brown adipose tissue:
a large amount of cytochromes
many mitochondria
rich blood supply
presence of thermogenic uncoupling protein
high ATP synthase activity

A

high ATP synthase activity

288
Q

Which of the following statements about NAD+ and NADP+ are true? 1) Both cofactors are derivatives of vitamin B1 (thiamine) 2) Both cofactors are derivatives of vitamin B3 (niacin, vitamin PP) 3) Both cofactors are derivatives of vitamin B6 (pyridoxol) 4) NAD+ and NADP+ participate in the processes of biological oxidation as hydrogen carriers 5) NAD+ and NADP+ are mainly cofactors of anaerobic dehydrogenases
1+3+4
3+4+5
2+4+5
2+3+5
1+4+5

A

2+4+5

289
Q

Choose the correct statements about glycogen metabolism: 1) glycogen is synthesized and stored only in the mitochondrial matrix 2) hepatic glycogen is utilized in the maintaining of blood glucose level between the meals 3) glucose-6-phosphate produced in the muscles passes through the cell membrane along the concentration gradient to the blood 4) hepatocytes of the liver contain the enzyme glucose-6 phosphatase, which releases free glucose 5) muscle glycogen is used only by muscle cells
1+2+3
1+2+5
2+4+5
1+3+4
1+3+5

A

2+4+5

290
Q

Which of the listed compounds are substrates of gluconeogenesis? 1) lactate 2) acetyl-CoA 3) glycerol 4) alanine, glutamate, aspartate 5) glucose
2+4+5
all of them
2+3+4
1+3+4
1+3+5

A

1+3+4

291
Q

Glutathione is:
tissue hormone
natural opiate
a natural antioxidant
a steroid compound

A

a natural antioxidant

292
Q

Which of the following metabolic disorders ARE NOT observed in diabetes type 2?
1) hyperglycemia
2) ketoacidosis
3) hypertriglyceridemia (elevated levels of VLDL)
4) hyperchylomicronemia
5) glucosuria
1+5
3+4
2+4
1+3
2+5

A

2+4

293
Q

Which of the biosynthetic processes are carried out with the participation of tetrahydrofolic acid derivatives as cofactors: 1) synthesis of purines (С2 and С8 atoms) 2) synthesis of choline from ethanolamine 3) synthesis of methionine from homocysteine 4) synthesis of creatine phosphate 5) synthesis of TMP from dUMP
1+3+5
2+3+5
1+2+3
3+4+5
2+3+4

A

1+3+5

294
Q

Choose the correct statements about the role of glycolysis in the body:
1) delivers reducing equivalents for anabolic pathways
2) supplies acetyl-CoA for the synthesis of ketone bodies
3) supplies substrates for the synthesis of essential amino acids
4) delivers energy to muscle cells during prolonged starvation
5) supplies acetyl-CoA for fatty acid synthesis
2+4+5
1+2+3
1+3
3+5
2+4

A

2+4

295
Q

cAMP-dependent protein kinase (PKA) phosphorylates: 1) glycogen synthase and inactivates it 2) glycogen synthase and activates it 3) glycogen phosphorylase kinase and activates it 4) glycogen phosphorylase kinase and inactivates it 5) glycogen phosphorylase and activates it
2+5
2+4
1+5
1+3
3+4

A

1+5

296
Q

Which of the following enzymes are components of the pyruvate dehydrogenase complex (PDH)? 1)acetyl-CoA carboxylase 2) pyruvate dehydrogenase 3) dihydrolipoyl transacetylase 4) dihydrolipoyl dehydrogenase 5) pyruvate kinase
3+4+5
1+3+4
1+2+4
2+4+5
2+3+4

A

2+3+4

297
Q

The unit of enzyme quantity (activity) in the International System of Units (SI) is Katal. One Katal (Kat) is the amount of the enzyme required to convert:
One mole of substrate for one second
One milimole of substrate per one minute
one milliliter of substrate per one minute
One micromole of substrate per one minute
One micromole of substrate for one second

A

One mole of substrate for one second

298
Q

Indicate the correct combinations of a neuromediator and the amino acid, form which it is synthesized. 1) gamma-aminobutirate from aspartate 2) gamma-aminobutirate from glutamate 3) serotonin from tryptophan 4) serotonin from tyrosine 5) dopamin from tyrosine
3+4+5
1+3+5
1+2+3
2+3+4
2+3+5

A

2+3+5

299
Q

Which of the following statements about cholesterol are true? 1) it is synthesized from acetyl-CoA 2) it’s synthesis occurs in the cytosol and in the endoplasmic reticulum 3) the main regulatory enzyme of cholesterol synthesis is HMG-CoA synthase 4) it is fully degraded in the liver 5) it’s synthesis is stimulated by insulin
1+3+4
1+2+5
1+3+5
2+4+5
3+4+5

A

1+3+5

300
Q

Which of the processes are specific to the liver only? 1) conversion of indirect bilirubin to direct bilirubin, 2) urea cycle, 3) glycogen synthesis, 4) cholesterol synthesis, 5) gluconeogenesis
3 + 5
1 + 2
4 + 5
2 + 3
1 + 4

A

1 + 2

301
Q

Which statements about thyroid hormones (T4 and T3) are true? 1) inhibit gluconeogenesis and glycogenolysis to prevent the formation of free glucose, 2) T3 is formed only in the thyroid gland, 3) T4 and T3 increase the synthesis and secretion of TSH, 4) T4 and T3 decrease the synthesis and secretion of TSH, 5) the enzyme thyroid peroxidase is involved in their synthesis
2 + 3
1 + 4
3 + 5
1 + 2
4 + 5

A

4 + 5

302
Q

Which is the WRONG statement?
a)VLDL transports triacylglycerols from the liver to the extrahepatic tissues
b)LDL contains only apo B-100
c) VLDL is metabolized to LDL after hydrolysis of triacylglycerols by hormone-sensitive lipase
d)the main components of LDL are cholesterol and cholesteryl esters
chylomicrons transport mainly triacylglycerols from the intestines to the liver and other tissues

A

a)VLDL transports triacylglycerols from the liver to the extrahepatic tissues

303
Q

Gout could be caused by:
a)complete deficiency of hypoxanthine/guanine phosphoribosyl transferase
b)a partial deficiency of xanthine oxidase
c)a partial deficiency of hypoxanthine/guanine phosphoribosyl transferase
d)abnormally increased activity of aspartate transcarbamoylase
deficiency of folic aci

A

complete deficiency of hypoxanthine/guanine phosphoribosyl transferase

304
Q

Which of the listed molecules are signaling molecules?
1) interleukins 2)acetylcholine
3) interferons
4) prostaglandins
5) leukotrienes
c) 2+4+5
d) 1+4+5
b) 1+3+4
all of them
a) 1+2+3

A

all of them

305
Q

What is the fate of hydrogen released in oxidative reaction in glycolysis? 1) used for the synthesis of fatty acids 2) under anaerobic conditions it is directed for pyruvate reduction 3) under aerobic conditions it is directed for pyruvate reduction 4) under aerobic conditions it is transferred to the matrix of mitochondria 5) directed for the reduction processes in the synthesis of cholesterol
2+4+5
1+3
2+4
3+5
1+2+3

A

2+4

306
Q

Which of the following symptoms is not typical for patients with diabetes:
hypoglycemia
ketoacidosis
polyuria
glucosuria

A

hypoglycemia

307
Q

Which of the following enzyme catalyzes the conversion of glucose to glucose-6-phosphate in muscle cells:
Hexokinase
Phosphoglucomutase
Glucose-6-phosphatase
Glucokinase

A

Glucose-6-phosphatase

308
Q

Which of the following pathways of glucose metabolism is not catabolic:
glycolysis
oxidative decarboxylation of pyruvate
pentose phosphate pathway
gluconeogenesis

A

gluconeogenesis

309
Q

Which of mentioned biomolecules is the major energetic source for skeletal muscles during their prolonged and medium-intensive activity (long distance running):
glucose
none of them
fatty acids
ketone bodies

A

ketone bodies

310
Q

Which of the following statements about the mechanism by which insulin affects the activity of glycogen synthase (regulatory enzyme of glycogenogenesis) is wrong:
1. the active protein phosphatase-1 catalyzes the phosphorylation of glycogen synthase (glycogen synthase a)
2.insulin decreases the level of cAMP, which leads to dropout of the activation of protein kinase A, catalyzing the formation of the active phosphorylated form of the protein, called “inhibitor-1”
3.the action of insulin gives the phosphorylated form of glycogen synthase (glycogen synthase b)
4.when the inhibitory protein-1 is inactive (dephosphorylated) it does not inhibit the activity of proteinphosphstase – 1

A

2.insulin decreases the level of cAMP, which leads to dropout of the activation of protein kinase A, catalyzing the formation of the active phosphorylated form of the protein, called “inhibitor-1”

311
Q

Which of the following alterations does not appear to be a reason for development of Diabetes type II (insulin-independent):
1.decreased affinity of the insulin receptor towards insulin
2.decreased synthesis of insulin receptors
3.synthesis of abnormal (defect) insulin
4.progressive destruction of the B-cells of pancreas by autoimmune mechanisms

A

4.progressive destruction of the B-cells of pancreas by autoimmune mechanisms

312
Q

Which of the following glycolytic enzymes catabolize the metabolic steps leading to the formation phosphoenolpyruvate:
enolase
glycerate kinase
aldolase
pyruvate kinase

A

pyruvate kinase

313
Q

The blood level of which of the mentioned metabolites is significantly increased during active muscle contraction:
amino acids
none of them
glucose
lactate

A

lactate

314
Q

Which of the following statements about the malate-aspartate shuttle is not true:
1.the pair of substrates involved in the shuttle are oxaloacetate and malate
2.the shuttle is bidirectional
3.transferred by the shuttle mechanism, two pairs of reducing equivalents after their submission to the respiratory chain, lead to the synthesis of 4 ATP molecules
4.cytoplasmic and mitochondrial malate dehydrogenase participate in shuttle

A

3.transferred by the shuttle mechanism, two pairs of reducing equivalents after their submission to the respiratory chain, lead to the synthesis of 4 ATP molecules

315
Q

Which of mentioned metabolic pathways in the liver for conversion of glucose do not occur during fasting (between meals):
1.gluconeogenesis
2.degradation of glycogen
3.degradation of glucose, in order to provide substrate for fatty acids synthesis
4.degradation of glucose-6-phosphste to glucose

A

4.degradation of glucose-6-phosphste to glucose

316
Q

Which of the following enzymes involved in gluconeogenesis, it is the most important regulatory enzyme in the process, subjected to allosteric regulation of variety of modulators:
pyruvate carboxylase
fructose-1,6-bisphosphatase
glucose-6-phosphatase
phosphoenolpyruvate-carboxykinase (PEPCK)

A

fructose-1,6-bisphosphatase

317
Q

Which of the following metabolites of glycolysis is obtained in an oxidation step and is a macroergic phosphate compound:
glyceraldehyde 3-phosphate
1,3-bisphosphoglycerate
phosphoenol pyruvate
pyruvate

A

1,3-bisphosphoglycerate

318
Q

Which of the mentioned mtabolites (substances) serves as an energetic source (alternative to glucose) during prolonged fasting:
fructose
glycerol
ketone bodies

A

ketone bodies

319
Q

Which of the following statements about the oxidative decarboxylation of pyruvate is wrong:
the product of oxidative decarboxylation of pyruvate is Acetyl CoA
oxidative decarboxylation of pyruvate is carried in multienzyme complex called pyruvate dehydrogenase complex
oxidative decarboxylation of pyruvate takes place in the mitochondria
NADP+ serves as a coenzyme in the pyruvate dehydrogenase complex and NADPH is obtained

A

NADP+ serves as a coenzyme in the pyruvate dehydrogenase complex and NADPH is obtained

320
Q

In which of the following cells an anaerobic glycolysis is performed:
white muscle fibers (during active contraction)
cells of the renal medulla
erythrocytes
cells of the crystalline lens

A

erythrocytes

321
Q

Which of the following glycolytic enzymes catalyzes an irreversible metabolic step:
glycerate kinase
aldolase
glyceraldehyde 3-phosphate dehydrogenase
pyruvate kinase

A

pyruvate kinase

322
Q

Which of the following hormones by its effect on the liver cells, results in the formation of active kinase dephosphorylated form of the enzyme phosphofructokinase 2:
Glucagon
Adrenaline
None of the mentioned above
Insulin

A

Insulin

323
Q

Which of the following pairs of hormones appears to be, depending on the quantitative ratio of their blood levels, the main regulator of the metabolism of energetic biomolecules (glucose, fatty acids):
insulin / glucagon
glucagon / cortisol
insulin / cortisol
glucagon / adrenaline

A

insulin / glucagon

324
Q

Which of the following enzymes involved in the breakdown of carbohydrates in the digestive tract of humans, have small intestine origin?
sucrose
glucoamylase
lactase
α- amylase

A

lactase

325
Q

Which of the following enzymes involved in glycogen metabolism, catalyzes the degradation of α-1,4-glycosidic bond:
phosphoglucomutase
amylo-1,4 → 1,6-transglucosidase
glycogen phosphorylase
glycogen synthase

A

glycogen phosphorylase

326
Q

In insufficiency of which of the following enzymes involved in the degradation of galactose, pathological condition known as galactose intolerance or galactosemia develops:
С4- epimerase
galactose-1-phosphate-uridil transferase
none of the mentioned above
Galactokinase

A

galactose-1-phosphate-uridil transferase

327
Q

To which of the following enzymes functioning in gluconeogenesis, acetyl-CoA is an allosteric activator:
glucose-6-phosphatase
PEPC
pyruvate carboxylase
fructose-1,6-bisphosphatase

A

pyruvate carboxylase

328
Q

Which of the following statements about the structure of glycogen is wrong:
glycogen molecule has a branched structure
in the straight sections of the polysaccharide chains glucose residues are joined by α-1,4-glycosidic bond
glycogen is heteropolysaccharide
in the branches sections in the polysaccharide chain the bond is α-1,6-glycosidic

A

glycogen is heteropolysaccharide

329
Q

Which of the following coenzymes is a cofactor of glyceraldehyde 3-phosphate dehydrogenase, which catalyses an oxidative step in glycolysis:
FMN
FAD
NAD+
NАDP+

A

NAD+

330
Q

Which of these metabolites is the allosteric activator of phosphorylated glycogen synthase b:
АTP
АМP
glucose-6-phosphate
fructose-2,6-bisphosphate

A

АМP

331
Q

Which of the following metabolites of glucose is a a key metabolite of glucose metabolism:
lactate
glucose 6-phosphate
fructose-1,6-biphosphate
pentose-5-phosphate

A

glucose 6-phosphate

332
Q

When you consider that for the synthesis of one molecule glucose in gluconeogenesis two molecules pyruvate are used, choose the correct answer of the question – how many molecules ATP are spent in the process of gluconeogenesis
3 molecules ATP
2 molecules ATP
6 molecules ATP
neither one single molecule ATP

A

6 molecules ATP

333
Q

In which of the following cell types malate-aspartate shuttle mechanism does not function:
hepatocytes
brain cells
kidney cells
heart muscle

A

brain cells

334
Q

Which of the following enzymes of the glycolytic metabolic chain catalyzes the step, occurring phosphorylation in the substrate chain, ie carries out the synthesis of ATP:
Phosphofructokinase 1
Phosphoglucomutase
Hexokinase
Pyruvatekinase

A

Phosphofructokinase 1

335
Q

In the failure of which of these enzymes involved in the catabolism of fructose the hereditary disease “congenital fructose intolerance” is developed:
triosokinase
none of the above mentioned
Fructokinase
Aldolase B

A

Aldolase B

336
Q

With the deficiency of which of the following enzymes of the pentose-phosphate pathway is associated the risk of hemolytic anemia:
Phosphogluconolaktonase
Transaldolase
Transketolase
Glucose-6-phosphate dehydrogenase

A

Glucose-6-phosphate dehydrogenase

337
Q

Which of the following metabolites pairs performes the transfer of reducing equivalents of NAD.H from the cytosol to the respiratory chain in malate-aspartate shuttle mechanism:
malate- aspartate
malate/oxaloacetate
none of the mentioned above
DHAP / glycerol-3-phosphate

A

malate- aspartate

338
Q

Which of the following statements about the metabolism of liver glycogen is true:
a.its digested in periods of fasting
b.glucagon stimulates its synthesis
c.adrenaline stimulates its synthesis
d.In its degradation lactate is released in the blood

A

In its degradation lactate is released in the blood

339
Q

Which of mentioned biomolecules is the major energetic source for skeletal muscles during their intensive and non-continuous contractions:
glucose
none of them
fatty acids
ketone bodies

A

fatty acids

340
Q

How many of the metabolic steps in glycolysis are irreversible
2
5
none
3

A

3

341
Q

Which of the following symptoms are typical for mono- and disaccharidases malabsorption (intolerance) and lactose intolerance?
1) diarrhea
2) intestinal distension
3) painful colics
4) meteorism
1+3
2+4
1+2+3
1+2+3+4

A

1+3

342
Q

Which of the following enzymes involved in the glycolysis is the major regulatory enzyme of glycolysis:
Phosphofructokinase-2 (PFK-2)
Phosphofructokinase-1 (PFK-1)
Phosphoglycerate kinase
Aldolase

A

Phosphofructokinase-1 (PFK-1)

343
Q

Which of the following metabolic steps of gluconeogenesis is common for glycolysis and gluconeogenesis:
fructose-1,6-bisphosphate → fructose-6-phosphate
oxaloacetate → phosphonenolpyruvate
pyruvate →oxaloacetate
fructose-6-phosphate → Glucose-6-phosphate

A

fructose-1,6-bisphosphate → fructose-6-phosphate

344
Q

By which of the following transports the transition of glucose through the luminal membrane of intestinal epithelial cells is performed:
active transport
enhanced diffusion and secondary active transport
passive diffusion
secondary active transport

A

secondary active transport

345
Q

Glycerol is a non-carbohydrate precursor for the synthesis of glucose in gluconeogenesis.To which of the following metabolites of gluconeogenesis turns the glycerol to:
phosphonenolpyruvate
pyruvate
dihydroxyacetone phosphate
fructose-6-phosphate

A

dihydroxyacetone phosphate

346
Q

Which of the listed deficiencies (of enzymes and / or vitamins) lead to lactic acidosis?
1)thiamine
2) erythrocyte enzymes of glycolysis
3) enzymes of pyruvate dehydrogenase complex
4) muscle enzymes of glycolysis

A

1)thiamine

347
Q

Glycosylated hemoglobin is an indicator of:
prolonged hyperglycaemia
prolonged hypoglycaemia
impaired pentose phosphate function
reduced glucose uptake into erythrocytes

A

prolonged hyperglycaemia

348
Q

Which of the following enzymes catalyzes the synthesis of fructose-2,6-bisphosphate, appearing as the strongest activator of the regulatory enzyme of glycolysis:
hexokinase
phosphofructokinase 2
phosphofructokinase 1
phosphoglycerate kinase

A

phosphofructokinase 2

349
Q

Which of the following statements about the enzyme glucose-6-phosphatase is wrong:
a.the highest concentration of enzyme is found in skeletal muscle cells
b.the synthesis of the enzyme is induced by the hormone cortisol
c.the enzyme is localized in the endoplasmic reticulum
d.the enzyme catalyzes the hydrolysis of glucose-6-phosphate to glucose-free, as it passes from the liver into the blood to maintain normal blood glucose level

A

a.the highest concentration of enzyme is found in skeletal muscle cells

350
Q

Which of the following statements about the transport of glucose from the blood into the cells of skeletal muscle is wrong:
a.the insulin induces the biosynthesis of an enzyme which catalyzes phosphorylation of b.the free glucose to glucose-6-phosphate
c.the transport is carried out by a glucose transporter (facilitated diffusion)
d.the glucose enters the cells of the skeletal muscle by the concentration gradient
e.insulin stimulates glucose transport through the export of glucose carriers from the cell on the cell membrane, i.e. - By increasing the number of transporters on the cell membrane

A

d.the glucose enters the cells of the skeletal muscle by the concentration gradient

351
Q

Which of the following statements about the influence of insulin on blood glucose level is wrong:
a.stimulates glycolysis in the liver
b.does not stimulate glucose transport in adipose tissue
c.reduces the level of blood glucose by accelerating its transport from the blood into d.insulin-dependent tissues
e.stimulates the synthesis of liver and muscle glycogen

A

b.does not stimulate glucose transport in adipose tissue

352
Q

In which of the following types of cells the transport of glucose is insulin-independent:
1) adipocytes
2) brain
3) skeletal muscle cells
4) erythrocytes

A

2) brain
4) erythrocytes

353
Q

Which amino acids are required for the synthesis of creatine phosphate?
1) tyrosine;
2) glycine;
3) arginine;
4) lysine;
5) methionine
1+2+5
2+3+5
1+2+3
1+3+4
2+4+5

A

2+3+5

354
Q

The simultaneous increase of the AST and ALT serum levels is used to diagnose a disease of the:
brain
muscules
stomach
prostate
liver

A

liver

355
Q

Which of the following chemical bonds/interactions are involved in stabilizing the tertiary structure of proteins?
1) ion, dipole and ion-dipole interactions;
2) hydrophobic interactions;
3) peptide bonds;
4) hydrogen bonds between radicals;
5) hydrogen bonds between closely spaced peptide groups
1+3+5
1+2+4
2+3+4
1+4+5
1+2+3

A

2+3+4

356
Q

Identify the true statements about glutamate dehydrogenase.
1) oxidatively deaminates glutamate together with NAD;
2) reductively aminates α-ketoglutarate together with NADPH;
3) oxidatively deaminates glutamate together with FAD;
4) it is activated allosterically by ATP and GTP
5) it is localized in the mitochondria.
1+2+4
1+2+5
2+3+4
1+4+5
2+3+5

A

2+3+5

357
Q

User
Which of the following changes are observed in hemolytic jaundice?
1) increased urobilinogen in urine;
2) increased bilirubin in urine;
3) very dark stools;
4) increased indirect bilirubin in serum; 5) increased direct bilirubin in serum.
1+2+3
1+3+4
1+4+5
2+3+4
2+4+5

A

1+3+4

358
Q

Heme biosynthesis is a process:
1) that is highly prevalent in the liver and bone marrow;
2) localized in mitochondria and cytosol of cells;
3) which is highly prevalent in mature erythrocytes;
4) which requires succinyl-CoA and glycine;
5) which requires carbamoyl phosphate and aspartate.
1+3+4
1+3+5
1+2+4
2+3+4
2+3+5

A

2+3+4

359
Q

Heme biosynthesis is a process:
1) that is highly prevalent in the liver and bone marrow;
2) localized in mitochondria and cytosol of cells;
3) which is highly prevalent in mature erythrocytes;
4) which requires succinyl-CoA and glycine;
5) which requires carbamoyl phosphate and aspartate.
1+3+4
1+3+5
1+2+4
2+3+4

A

1+2+4

360
Q

Indicate the correct answers describing the features of the protein ubiquitin.
1) it is a protein fragment obtained as a result of the proteolytic maturation of the insulin molecule;
2) it is a protein fragment obtained as a result of the proteolytic maturation of pituitary hormones;
3) it is a small protein that binds covalently to other proteins through its glycine terminal carboxyl group and marks them for subsequent degradation;
4) it is an enzyme that is found in all cells and participates in processes of proteolytic maturation of hormones;
5) it is a protein through which the cell directs “aged” proteins to the proteasome, where they are degraded.
1 + 3
2 + 3
3 + 4
3 + 5
4 + 5

A

3 + 5

361
Q

The chemical bond between the pentose and the phosphoric acid in nucleotides is:
О-glycosidic
N-glycosidic
phosphodiester bond
ester bond
peptide bond

A

phosphodiester bond

362
Q

Which of the end products of heme degradation are increased in parenchymal jaundice?
1) urobilinogen in urine;
2) bilirubin in urine;
3) indirect bilirubin in serum;
4) direct bilirubin in serum;
5) stercobilin in feces.
2+4
1+3
1+2
3+4
4+5

A

4+5

363
Q

Carbamoylphosphate synthetase I, supplying carbamoylphosphate for the urea cycle:
1) is located in the mitochondria of hepatocytes;
2) is located in the cytosol of hepatocytes;
3) is a regulatory enzyme;
4) is activated allosterically by N-acetylglutamate;
5) is activated allosterically by N-acetylglutamine.
1+2+4
1+4+5
3+4+5
1+3+4
2+3+5

A

1+2+4

364
Q

Which of the following enzymes in the synthesis of purine nucleotides are under allosteric control?
1) phosphoribosylpyrophosphate synthetase;
2) formyl transferase;
3) glutamine-phosphoribosylpyrophosphate amidotransferase;
4) adenylosuccinate lyase;
5) xanthine oxidase.
2+5
1+3
1+4
2+3
4+5

A

1+3

365
Q

Which of the following molecules are produced when heme is broken down?
1) uric acid;
2) bilirubin;
3) biliverdin;
4) urea;
5) creatinine.
1+2
1+3
2+3
3+4
2+5

A

2+3

366
Q

Heme is a cofactor of:
1) phosphofructokinase-1;
2) citrate synthase;
3) cytochromes;
4) ATP synthase;
5) catalase.
1+2
2+3
3+4
4+5
3+5

A

3+5

367
Q

Tyrosine is the precursor for the synthesis of:
1) NAD;
2) melanine;
3) melatonin;
4) thyroid hormones;
5) corticosteroids.
1+2
2+4
2+3
2+5
4+5

A

2+3

368
Q

Which disease occurs with a genetic defect in an enzyme that breaks down valine, isoleucine, and methionine?
pellagra
alkaptonuria
merhylmalonylemina
albinism
Lesch-Nyhan syndrome

A

merhylmalonylemina

369
Q

What features are characteristic of hemoglobin?
1) consists of 4 different polypeptide chains;
2) consists of 4 polypeptide chains, two by two identical;
3) each polypeptide chain contains heme;
4) heme iron is divalent;
5) heme iron is trivalent.
1+3+5
2+3+5
1+3+4
2+3+4
1+2+3

A

2+3+4

370
Q

The breakdown of heme produces:
1) carbon monoxide;
2) carbon dioxide;
3) bile acids;
4) bile pigments;
5) uric acid.
4+5
1+4
1+2
2+3
1+5

A

4+5

371
Q

Indicate the true statements about folic acid.
1) its active form is tetrahydrofolate;
2) its active form is dihydrofolate;
3) supplies one-carbon groups for the synthesis of the purine ring;
4) supplies one-carbon groups for the synthesis of the pyrimidine ring;
5) supplies one-carbon groups for creatine synthesis.
2+4
4+5
1+3
1+2
3+5

A

1+3

372
Q

Identify the true statements about the synthesis of pyrimidine nucleotides.
1) the pyrimidine ring is built on a ribose phosphate residue;
2) the pyrimidine ring is formed first and then a ribose phosphate residue is added to it;
3) tetrahydrofolate derivatives are needed to obtain dTMP;
4) S-adenosylmethionine is required to produce dTMP;
5) all enzymes have a cytosolic localization.
2+5
1+3
1+2
2+3
4+5

A

2+3

373
Q

Identify the true statements about phenylketonuria.
a. It is caused by deficiency of phenylalanine hydroxylase.
b. It is caused by hyperactive phenylalanine hydroxylase.
c. It is characterized by an accumulation of homogentisinate
d. It is characterized by an accumulation of tryptophan.
e. It is caused by reduced activity of dihydrofolate reductase.

A

a. It is caused by deficiency of phenylalanine hydroxylase.
c. It is characterized by an accumulation of homogentisinate

374
Q

The nitrogen atom in carbamoyl phosphate required for the synthesis of pyrimidines originates from:
glutamate
ammonia
aspartate
glutamine
glycine

A

ammonia

375
Q

Which vitamin is present in the structure of FAD and FMN?
Vit B1 (thiamin)
Vit B2 (riboflavin)
Vit B3 (niacin)
Vit B9 (folic acid)
Vit B12 (cobalamin)

A

Vit B2 (riboflavin)

376
Q

Which of the following compounds is NOT a metabolite involved in porphyrin biosynthesis?
porphobilinogen
glycine
succinyl-CoA
uroporphyrinogen
UDP-glucuronate

A

UDP-glucuronate

377
Q

Which of the following reactions requires S-adenosylmethionine as a methyl group donor?
The conversion of norepinephrine to epinephrine
The conversion of phenylalanine to tyrosine.
The synthesis of purines.
The conversion of dUMP to dTMP.
The conversion of glutamate to glutamine.

A

The conversion of norepinephrine to epinephrine

378
Q

Which of the following compounds is a cofactor of the enzymes heme oxygenase and biliverdin reductase?
UDP-glucoronate
NADH
pyridoxal phosphate
NADPH
ascorbic acid

A

NADPH

379
Q

Which are the regulatory enzymes in the synthesis of pyrimidine nucleotides?
1) carbamoyl phosphate synthetase II;
2) dihydroorotase;
3) dihydroorotate dehydrogenase;
4) aspartate transcarbamoylase;
5) carbamoyl phosphate synthetase I.
1+3
1+4
2+5
3+5
4+5

A

1+4

380
Q

Cytotoxic ammonia is neutralized by:
1) the synthesis of glutamine in the brain;
2) the synthesis of alanine in muscles; 3) transdeamination reactions;
4) formation of ammonium ions in the brain;
5) reductive amination of alpha-ketoglutarate.
1+2+4
1+2+5
2+3+4
1+4+5
2+3+5

A

1+2+5

381
Q

Which biosynthetic processes take place with the participation of tetrahydrofolic acid derivatives as cofactors?
1) the synthesis of purines (C2 and C8 atoms);
2) the synthesis of choline from ethanolamine;
3) the synthesis of methionine from homocysteine;
4) creatine synthesis;
5) the synthesis of TMF.

A

1) the synthesis of purines (C2 and C8 atoms);
3) the synthesis of methionine from homocysteine;
5) the synthesis of TMF.

382
Q

Which of the following enzymes in the synthesis of pyrimidine nucleotides are under allosteric control?
1) carbamoyl phosphate synthetase II; 2) dihydroorotase;
3) dihydroorotate dehydrogenase;
4) aspartate transcarbamoylase;
5) orotate phosphoribosyltransferase.
2+5
1+4
1+3
3+4
1+5

A

1+4

383
Q

Tyrosinemias are observed in genetically determined insufficiency of enzymes from the catabolite chain of:
histidine
tryptophan
valine
leucine
phenylalanine

A

phenylalanine

384
Q

Which amino acids are sources of one-carbon residues for tetrahydrofolic acid?
serine, histidine, arginine
serine, tyrosine, tryptophan
histidine, glycine, valine
tryptophan, histidine, glutamate
serine, histidine, tryptophan

A

serine, histidine, arginine

385
Q

The function of haptoglobin is:
1) to bind free heme;
2) to participate in the synthesis of hemoglobin for erythrocytes;
3) to transport the hemoglobin/haptoglobin complex through the kidneys;
4) to prevent loss of hemoglobin from the kidneys;
5) to preserve iron in the body.
3+5
1+3
2+4
4+5
1+2

A

3+5

386
Q

Which statements are true about the hormone hepcidin?
1) increases serum iron content;
2) lowers serum iron content;
3) binds to the iron exporter ferroportin; 4) binds to the iron transport protein transferrin;
5) binds to the iron-depositing protein ferritin.
2+5
1+3
1+4
2+3
4+5

A

2+3

387
Q

Protein denaturation is a process that: 1) changes the amino acid composition of the protein molecule;
2) destroys the primary structure of the protein molecule;
3) leads to loss of biological activity of the protein;
4) increases the chemical reactivity of the polypeptide chain of the protein;
5) destroys the secondary, tertiary and quaternary level of organization of the protein
1+2+5
3+4+5
1+2+3
2+3+5
1+3+4

A

2+3+5

388
Q

Which cofactors are involved in the oxidative decarboxylation of α-keto acids?
1) NAD+;
2) NADP+;
3) lipoic acid;
4) ascorbic acid;
5) coenzyme A (CoA-SH).
1+3+4
1+3+5
2+3+4
2+3+5
3+4+5

A

1+3+5

389
Q

The amino acid arginine is NOT a precursor for the synthesis of:
creatine phosphate
ethanolamine
nitric oxide
ornithine
polyamines

A

ethanolamine

390
Q

Which nucleotide is a secondary mediator of the action of adrenaline in muscles and glucagon in liver?
ATP
ADP
AMP
cyclic 3’,5’-АMP
cyclic 3’,5’-GMP

A

AMP

391
Q

Which of the following statements about the quaternary structure of proteins are true?
1) the achievement of such a structure is due to non-covalent (weak) interactions between two or more polypeptide chains;
2) proteins with a quaternary structure represent supramolecular complexes made up of two or more polypeptide chains (subunits) connected by covalent bonds;
3) the quaternary structure is mandatory for the manifestation of the biological activity of proteins;
4) the quaternary structure is necessary for those proteins that will be targeted for degradation;
5) the acquisition of a quaternary structure is one of the reasons for the existence of different isoforms and regulation in some proteins.
1+5
1+3
2+4
3+5
1+4

A

1+5

392
Q

Which of the following statements about the urea cycle are true?
1) occurs in the mitochondria and the cytosol;
2) occurs in endoplasmic reticulum and cytosol;
3) proceeds in the liver;
4) occurs intensively after taking a balanced meal;
5) does not require energy.
3+5
1+2
4+5
1+3
2+4

A

1+3

393
Q

Name the enzymes involved in the folding of polypeptide chains.
1) prolyl cis-trans isomerase;
2) protein disulfide isomerase;
3) prolyl hydroxylase;
4) lysyl hydroxylase;
5) chaperones.
1+2+5
2+3+4
1+2+3
1+4+5
1+3+4

A

1+2+5

394
Q

Which of the following statements about nucleosides are true?
1) they consist of nitrogen base and pentose;
2) in the structure of nucleic acids they are connected by 3’-5’-phosphodiester bonds;
3) The N-glycosidic bond between the base and the pentose in purine nucleosides is at N1;
4) The N-glycosidic bond between the base and the pentose in pyrimidine nucleosides is at N1;
5) syn-conformers of nucleosides predominate.
3+5
3+4
1+2
1+4
2+5

A

1+4

395
Q

Which of the following chemical bonds/interactions are involved in stabilizing the secondary structure of proteins?
ion, ion-dipole, dipole interactions
hydrogen bonds between side radicals of closely positioned amino acids
peptide bonds
disulfide bonds
hydrogen bonds between closely positioned peptide groups

A

hydrogen bonds between side radicals of closely positioned amino acids

396
Q

Identify the correct neurotransmitter/amino acid combination from which the corresponding neurotransmitter is synthesized.
gamma-aminobutirate from glutamate
gamma-aminobutirate from aspartate
serotonin from tyrosine
serotonin from sulfur-containing amino acids
norepinephrine and epinephrine from tryptophan

A

gamma-aminobutirate from glutamate

397
Q

Which of the following statements about heme synthesis are true?
1) the main regulatory enzyme is δ-aminolevulinate (ALA) dehydratase;
2) the main regulatory enzyme is δ-aminolevulinate (ALA) synthase;
3) heme is a major allosteric inhibitor of the regulatory enzyme;
4) porphyria can develop with ALA-synthase deficiency;
5) heme is synthesized in the bone marrow and liver.
2+4+5
1+3+4
2+3+5
1+4+5
1+2+3

A

2+4+5

398
Q

Which of the following proteins are involved in iron transport?
1) transferrin;
2) ceruloplasmin;
3) lactoferrin;
4) ferritin;
5) hemosiderin.
2+5
1+3
1+2
2+4
4+5

A

1+3

399
Q

How are purine nucleotides synthesized in the “de novo” pathway?
1) the synthesis starts from carbamoyl phosphate and aspartate;
2) synthesis starts from glycine and aspartate;
3) the purine ring is built by attaching atoms to phosphoribosylpyrophosphate;
4) the phosphoribosyl residue joins an already formed purine ring;
5) glycine and glutamine are involved in the synthesis.
1+2
2+4
2+5
3+5
4+5

A

1+2

400
Q

Which of the following statements about the iron metabolism is true?
physiologically, iron is deposited in the form of hemosiderin
transferrin can only bind heme iron
transferrin can only bind the ferrous (Fe2+) form of iron
hepcidin lowers serum iron by blocking ferroportin
hepcidin lowers serum iron by activating ferroportin

A

hepcidin lowers serum iron by blocking ferroportin

401
Q

In transamination:
1) amino acids are converted into biogenic amines;
2) one amino acid is converted to a keto acid and another keto acid is converted to an amino acid;
3) pyridoxal phosphate is involved as a cofactor;
4) amino groups of amino acids are released as free ammonia;
5) NADPH is involved as a cofactor
1+2
2+4
2+3
2+5
4+5

A

2+3

402
Q

Heme biosynthesis is a process:
1) that is highly prevalent in the liver and bone marrow;
2) localized in mitochondria and cytosol of cells;
3) which is highly prevalent in mature erythrocytes;
4) which requires succinyl-CoA and glycine;
5) which requires carbamoyl phosphate and aspartate.
1+3+4
1+3+5
1+2+4
2+3+4

A

1+2+4

403
Q

Which of the following substances are ketone bodies with metabolic importance for tissues:
1)acetoacetate
2) oxaloacetate
3) β- hydroxybutyrate
4) acetone
1+2+3
2+3+4
2+3
1+3

A

1+3

403
Q

Which of the following cofactors supplies reducing equivalents for the action of the enzyme HMG-CoA reductase?
NADP.Н
none of the above mentioned
FAD.Н2
NAD.H

A

NAD.H

404
Q

Which of the enzymes who catalyze reactions in the synthesis of glycerolipids is regulatory?
glycerol-3P-acyltransferase
phosphatide phosphatase
phosphatidylinositol synthase
diacylglycerol acyltransferase

A

diacylglycerol acyltransferase

405
Q

Which of the following statements for the synthesis of saturated fatty acids with an even number of carbon atoms (palmitic acid) is false?
synthesis takes place in the cytosol
NAD.H serves as a donor of reducing equivalents
NADP.H serves as a donor of reducing equivalents
direct substrate for the synthesis is malonyl-CoA

A

NAD.H serves as a donor of reducing equivalents

406
Q

Which of the following statements about the regulation of enzyme activity of 7α-hydroxylase which regulates the conversion of cholesterol to bile acids in the liver is false?
a. the catalytic activity of 7α-hydroxylase is regulated by phosphorylation / dephosphorylation, and the active form of b. the enzyme is dephosphorylated
c. bile acids inhibit the enzyme
d. cholesterol activates 7α-hydroxylase
e. in vit. C deficiency catalyzed by 7α-hydroxylase metabolic step slows down

A

d. cholesterol activates 7α-hydroxylase

407
Q

Which of the following coenzymes serves as a donor of reducing equivalents in the synthesis of fatty acids in acyl synthetase complex?
FMN.Н2
FAD.Н2
NADP.Н
NAD.Н

A

NADP.Н

408
Q

A key metabolite in the synthesis of cholesterol and ketone bodies is a one of the following compounds:
a. mevalonic acid
b. NADPН+Н+
c. 3-hydroxy-3-methylglutaryl-CоА
d. squalene

A

c. 3-hydroxy-3-methylglutaryl-CоА

409
Q

Which of the following statements about the physiological functions of eicosanoids is false?
a. participate in inflammatory processes in injuries and infections
b. all eicosanoids act as vasoconstrictors
c. some of them regulate smooth muscle contractions (intestine, uterus)
d. some of the eicosanoids are involved in platelet aggregation

A

b. all eicosanoids act as vasoconstrictors

410
Q

Increased concentrations of which of these transport forms of lipids decreases the risk of developing atherosclerosis and coronary heart disease?
LDL
IDL
VLDL
HDL

A

HDL

411
Q

Which of the following biological functions of cholesterol is not true?
a. cholesterol serves as a precursor for bile acids synthesis
b. cholesterol serves as a precursor for steroid hormone synthesis
c. cholesterol serves as a precursor for vitamin E synthesis
d. cholesterol participates in the construction of the cell e. membranes as a stabilizing component

A

c. cholesterol serves as a precursor for vitamin E synthesis

412
Q

Oxidation of unsaturated fatty acids occurs in:
mitochondria
cytoplasm
lysosomes
endoplasmic reticulum

A

endoplasmic reticulum

413
Q

Which of the following mechanisms activating the biosynthesis of fatty acids from insulin is incorrect?
a. insulin with its action gives the active nonphosphorylated form of the regulatory enzyme acetyl-CoA carboxylase
b. insulin with its action activates the enzyme glycerol-3-phosphate acyl transferase, forming its nonphosphorilated
c. insulin with its action induces the biosynthesis of the regulatory enzyme of fatty acid synthesis - acetyl-CoA carboxylase
d. insulin with its action induces the biosynthesis the multifunction enzyme of acyl synthetase complex (АSC)

A

b. insulin with its action activates the enzyme glycerol-3-phosphate acyl transferase, forming its nonphosphorilated

414
Q

Which of the following types of lipids is not a component of the membrane structures?
cholesterol
triacylglycerols
cardiolipins
phosphatidylethanolamine

A

triacylglycerols

415
Q

Which of the following reactions and processes provide reducing equivalents (NADPH) used in the synthesis of FA?
1) anaerobic glycolysis
2) pentose phosphate pathway
3) reaction catalyzed by malate dehydrogenase
4) reaction catalyzed by malate enzyme
2+3
2+4
2+3+4
1+2+3

A

2+3

416
Q

Which of the following statements about the metabolism of energetic biomolecules in a patient suffering from a carnitine deficiency is wrong?
there will be deficiency of ATP for gluconeogenesis leading to lowering glucose level in the blood (hypoglycaemia) in fasting state.

the levels of fatty acids in the blood will be low

the transport of long-chain fatty acids into the mitochondria of hepatocytes will be reduced and β-oxidation of fatty acids will be slower

ketone bodies synthesis will be reduced and their level in the blood will be low

A

the levels of fatty acids in the blood will be low

417
Q

Which of the following compounds are cholesterol derivatives?
1)aldosterone
2) adrenaline
3)cortisol
4)cholic acid
3+4
1+2+3
1+3
1+3+4

A

1+3

418
Q

Which enzyme is involved in the synthesis of cholesterol esters in HDL?
lecithin - cholesterol acyltransferase (LCAT)
Acetyl-CoA-cholesterol acyltransferase-(ACAT)
Pancreatic lipase
hormone-dependent lipase

A

lecithin - cholesterol acyltransferase (LCAT)

419
Q

Eicosatetraenoic acid (C20, 4:5,8,11,14) is a precursor for the synthesis of:
1) prostanoids with 2 double bonds
2) leukotrienes with 3 double bonds
3) lipoxins with 4 double bonds
4) none of the above mentioned
1+3
2+4
1+2+3
none

A

2+4

420
Q

Which of the following hormones stimulates ketogenesis in periods of fasting?
cortisol
glucagon
none of the above mentioned
insulin

A

glucagon

421
Q

How many metabolic steps are required for the decoupling (oxidation) of each two-carbon fragment of the long fatty acid chain in β-oxidation?
8
4
6
2

A

4

422
Q

Which of the following types of genetic defects, leading to development of inherited hyperlipoproteinemias, is the cause of familial hypercholesterolemia, characterized by elevated blood levels of LDL and considered as a risk factor for atherosclerosis?

genetic defects affecting enzymes (for example, lipoprotein lipase or lecithin-cholesterol acyltransferase-) involved in the metabolism of lipoproteins

genetic defects resulting in decreased synthesis of receptor LDL

none of them

genetic defects affecting the synthesis, structure, or secretion of apoproteins

A

genetic defects resulting in decreased synthesis of receptor LDL

423
Q

Which of the following compounds is a key (a key metabolite) in the synthesis of most glycerolipids?
phosphatidic acid
choline
CDP-choline
CDP- diacylglycerol

A

CDP- diacylglycerol

424
Q

Which of the following metabolites is a product of the degradation of ketone bodies (ketolysis)?
acetyl-CоА
malonyl -CоА
none of the above mentioned
succinyl -CоА

A

acetyl-CоА

425
Q

The oxidative phase of the PPP (pentose phosphate pathway) is important for:
1) cholesterol synthesis
2) synthesis of ATP
3) FA synthesis
4) gluconeogenesis
none
2+4
1+3
1+2+3

A

1+3

426
Q

Which of the following pathways of lipid metabolism occurring in adipose tissue is stimulated by insulin?
fatty acids synthesis (lipogenesis)
none of them
triacylglycerols degradation (lipolysis)
fatty acids degradation (β-oxidation)

A

fatty acids synthesis (lipogenesis)

427
Q

Which of the following essential polyunsaturated FA (PUFA) are supplied only from foods of animal origin.
1)linoleic acid
2)arachidonic acid
3)eicosapentaenoic acid
4)linolenic acid
2+3+4
2+3
1+4
1+2+3

A

2+3

428
Q

Which of the following compounds is the direct donor of 14 of the 16 carbon atoms in the synthesis of palmitic acid?
malonyl-CоА
acyl-CоА
acetyl-CоА
methilmalonyl-CоА

A

acetyl-CоА

429
Q

Which of the following lipoprotein complexes transport the “Bad” cholesterol and raising of their levels is a risk factor for atherosclerosis?
LDL
VLDL
HDL
chylomicrons

A

VLDL

430
Q

Which of the following biological effects are typical for PGE2?

1)bronchoconstrictor
2)vasodilator
3)inhibits the secretion of gastric juice
4) inhibits the uterine contractions
2+4
2+3+4
1+2+3
2+3

A

2+3+4

431
Q

Which of the following enzymes is regulatory in degradation of triacylglycerols in adipose tissue?
lipoprotein lipase
adipolitic lipase
phospholipase
glycerol kinase

A

adipolitic lipase

432
Q

Which of the following statements about the activity of the regulatory enzyme of fatty acid biosynthesis, acetyl-CoA carboxylase is false?
the activity is influenced by the action of hormones,as insulin stimulates the enzymatic activity

the activity is regulated by the mechanism of covalent modification (phosphorylation / dephosphorylation), аs the active form is phosphorylated.

the activity is regulated by the mechanism of covalent modification (phosphorylation / dephosphorylation), the active form is dephosphorylated.

the activity of the enzyme is regulated allosterically as citrate is allosteric activator

A

the activity is regulated by the mechanism of covalent modification (phosphorylation / dephosphorylation), аs the active form is phosphorylated.

433
Q

Which of the following statements about ketone bodies is wrong?
substrate for the synthesis of ketone bodies is acetyl CoA,
obtained from the oxidative decarboxylation of pyruvate

ketone bodies are acetoacetate, β-hydroxybutyrate and acetone, as acetone is product of acetoacetate degradation.

ketone bodies are an energy source alternative of glucose
the concentration of the β-hydroxybutyrate in the blood is usually higher than that of the acetoacetate

A

ketone bodies are acetoacetate, β-hydroxybutyrate and acetone, as acetone is product of acetoacetate degradation.

434
Q

Which of the following nucleoside-triphosphate is used to activate the so-called “polar head” in the synthesis of phosphoglycerides?
GTP
CTP
none of them
UTP

A

CTP

435
Q

Arachidonic acid is converted to biologically active eicosanoids in two metabolic pathways: cyclooxygenase and lipoxygenase. Which of the following statements about obtaining the eicosanoids is wrong?

aspirin is an irreversible inhibitor of the enzyme lipoxygenase

lipoxins are obtained by successively co action of 2 lipoxygenases

in the lipoxygenase pathway occurs the synthesis of leukotrienes

in the cyclooxygenase pathway the synthesis of prostaglandins and thromboxanes is performed

A

aspirin is an irreversible inhibitor of the enzyme lipoxygenase

436
Q

Which of the following foods does not supply cholesterol in the human body?
brain
liver
egg yolk
sunflower seeds

A

sunflower seeds

437
Q

Which of the following enzymes catalyze the hydrolysis of triacylglycerols located in different lipoprotein complexes (eg. in chylomicrons, VLDL)?
lecithin-cholesterol-acyltransferase
lipoprotein lipase
pancreatic lipase
adipolithyc lipase

A

lipoprotein lipase

438
Q

In which of the following cell compartments, except mitochondria, the oxidation of fatty acids may occur?
cytosol
endoplasmic reticulum
peroxisomes
lysosomes

A

peroxisomes

439
Q

In which of the following compartments of hepatocytes ketogenesis occurs ?
endoplasmic reticulum
cytosol
lysosomes
mitochondria

A

mitochondria

440
Q

By which of the following shuttle mechanisms the transfer of activated fatty acids from the cytosol into the mitochondria is performed?
acyl-carnitine
none of the above mentioned
malate-aspartate
glycero phosphate

A

acyl-carnitine

441
Q

At which positions in the fatty acids’ chains double bonds are introduced in humans ?
5, 8, 11 and 14
4, 5, 6 and 9
Опция 4
4, 5, 8 and 9

A

4, 5, 8 and 9

442
Q

Which of the following enzymes play an important role in the metabolism of lipoprotein complexes:
1)hepatic lipase
2)pancreatic lipase
3)lipoprotein lipase
4)LCAT (lecithin cholesterol acyltransferase)
3+4
1+2
1+3+4
1+2+3

A

1+2

443
Q

By which of the following substances the bile acids are conjugated (primary bile acids)?
none of them
glutathione
glucuronic acid
taurine

A

taurine

444
Q

Which of the following statements about the cholesterol synthesis is wrong?
cholesterol synthesis begins in the cytosol and continues and ends in the endoplasmic reticulum (microsomal fraction)

in the human body a large amount of cholesterol is synthesized in the intestinal mucosal cells
over 50% of the cholesterol in the human body resulted from endogenous synthesis

cholesterol synthesis occurs in the mitochondria

A

cholesterol synthesis occurs in the mitochondria

445
Q

Which of the following statements about the activation of fatty acids before their inclusion in β-oxidation is wrong?

activation of fatty acids is by connecting them with coenzyme A and turning them into acyl CoA derivatives

activation of the fatty acids takes place in the mitochondrial matrix

long chain fatty acids are activated

activation of the fatty acids takes place in the endoplasmic reticulum

A

activation of the fatty acids takes place in the endoplasmic reticulum

446
Q

How are the low-density lipoproteins (LDL) are assumed by the cells (entering from the blood into the cells)?
by passive diffusion
by facilitated diffusion
by receptor-mediated endocytosis
by secondary active transport

A

by receptor-mediated endocytosis

447
Q

In which of the following organs takes place the synthesis of ketone bodies (ketogenesis)?
skeletal muscle
brain
liver
heart muscle

A

liver

448
Q

Which of the following lipoprotein complexes are the basic carriers of TAG to peripheral tissues:
1)Chylomicrons
2)VLDL
3)LDL
4)HDL
1+2+3
1+2
1+3+4
3+4

A

1+2

449
Q

Which of the following compounds are not allosteric activators of the main key enzyme in the synthesis of FA, Acetyl CoA carboxylase?
1) acyl-CоА
2)acetyl-CоА
3)malonyl-CоА
4)citrate
1+2+3
2+4
2+3
2+3+4

A

2+4

450
Q

All of the following fatty acids are synthesized in the human body by the exception of one. Which is it?
palmitic acid
linoleic acid
oleic acid
stearic acid

A

linoleic acid

451
Q

Which of the following groups of lipids are glycolipids?
1)sphingomyelins
2)gangliosides
3)cerebrosides
4)lecithins
1+2+3
2+3+4
1+4
2+3

A

2+3

452
Q
  1. Which of the following enzymes, involved in the breakdown of carbohydrates in the digestive tract of humans, has/have small intestine origin?
    1) sucrase
    2) glucoamylase
    3) lactase
    4) α- amylase
    a) 1+2+3
    b) 1+3
    c) 2+4
    d) 4
A

a) 1+2+3

453
Q
  1. Which of the following symptoms are typical for mono- and disaccharidases malabsorption (intolerance) and lactose intolerance?
    1) diarrhea
    2) distension the intestine
    3) painful colics
    4) meteorism
    a) 1+2+3
    b) 1+3
    c) 2+4
    d) 1+2+3+4
A

d) 1+2+3+4

454
Q
  1. Which of the following enzymes involved in the glycolysis is the major regulatory enzyme of this pathway:
    a) Phosphofructokinase-2 (PFK-2)
    b) Aldolase
    c) Phosphoglycerate kinase
    d) Phosphofructokinase-1 (PFK-1)
A

d) Phosphofructokinase-1 (PFK-1)

455
Q
  1. In which of the following cells the anaerobic glycolysis is performed:
    1) white muscle fibers (during active contraction)
    2) cells of the renal medulla
    3) erythrocytes
    4) cells of the eye lens
    a) 1+2+3
    b) 1+3
    c) 2+4
    d) 1+2+3+4
A

d) 1+2+3+4

456
Q
  1. Which of the following substances is a direct product of the action of the enzyme glycogen phosphorylase (glycogenolysis):
    a) Glucose-6-phosphate
    b) Glucose
    c) Glucose-1-phosphate
    d) None of the mentioned above
A

c) Glucose-1-phosphate

457
Q
  1. Which of the following enzymes uses NAD.H as coenzyme in reduction process in anaerobic glycolysis:
    a) Pyruvate kinase
    b) Enolase
    c) Lactate dehydrogenase
A

c) Lactate dehydrogenase

458
Q
  1. Which of the following statements about the malate-aspartate shuttle is not true:
    a) The shuttle is bidirectional
    b) Cytoplasmic and mitochondrial malate dehydrogenases participate in the shuttle
    c) The oxidation in the respiratory chain of the two pairs of reducing equivalents transferred by the shuttle mechanism, leads to the synthesis of 4 ATP molecules
    d) The pair of substrates involved in the shuttle are oxaloacetate and malate
A

c) The oxidation in the respiratory chain of the two pairs of reducing equivalents transferred by the shuttle mechanism, leads to the synthesis of 4 ATP molecules

459
Q
  1. Which of the following co-enzymes serve as such of the enzyme of the pentose phosphate pathway, transketolase, and by measuring the enzymatic activity of transketolase is diagnosed a possible deficiency of this vitamin in the body:
    a) pyridoxal phosphate
    b) thiamine pyrophosphate
    c) NADP
    d) FAD
A

b) thiamine pyrophosphate

460
Q
  1. In which of the following types of cells the transport of glucose is insulin-independent:
    1) adipocytes
    2) brain
    3) skeletal muscle cells
    4) erythrocytes
    a) 1+2+3
    b) 1+3
    c) 2+4
    d) None of the above mentioned
A

c) 2+4

461
Q
  1. Which of the following statements about the pentose phosphate pathway in mature erythrocytes is true:
    a) Provides ribose-5-phosphate for the synthesis of nucleotides
    b) Provides NADPH for fatty acid synthesis
    c) Provides NADPH for maintaining the level of reduced glutathione, necessary for the disposal of Н2О2
    d) Provides NADPH of cholesterol synthesis
A

c) Provides NADPH for maintaining the level of reduced glutathione, necessary for the disposal of Н2О2

462
Q
  1. Which of the following statements about the transport of glucose from the blood into the cells of skeletal muscle is wrong:
    a) the transport is carried out by a glucose transporter (facilitated diffusion)
    b) insulin stimulates glucose transport through the export of glucose carriers on the cell membrane, i.e. by increasing the number of transporters on the cell membrane
    c) the glucose enters the cells of the skeletal muscle along the concentration gradient
    d) Insulin induces the biosynthesis of an enzyme which catalyzes phosphorylation of the free glucose to glucose-6-phosphate
A

d) Insulin induces the biosynthesis of an enzyme which catalyzes phosphorylation of the free glucose to glucose-6-phosphate

463
Q
  1. Which of the following statements about the metabolism of liver glycogen is wrong:
    a) it is synthesized after carbohydrate-rich food intake
    b) insulin stimulates its synthesis
    c) it is broken down in conditions with high blood glucose levels
    d) by degradation it provides blood glucose
A

d) by degradation it provides blood glucose

464
Q

d) phosphoenolpyruvate-carboxykinase (PEPKK)
29. Which of the following hormones stimulates the gluconeogenesis by inducing biosynthesis of phosphoenolpyruvate-carboxykinase (PEPKK) and other specific enzymes of gluconeogenesis:
a) Cortisol
b) Insulin
c) Aldosterone
d) Adenocorticotropic hormone (ACTH)

A

a) Cortisol

465
Q
  1. Which of the following statements about the effects of cortisol on the blood glucose level is correct:
    a) cortisol increases blood glucose level by stimulating the glycogenolysis
    b) cortisol increases blood glucose level by stimulating gluconeogenesis
    c) cortisol decreases blood glucose level by increasing the uptake of glucose into cells
    d) cortisol decreases blood glucose level by stimulating the glycolysis
A

b) cortisol increases blood glucose level by stimulating gluconeogenesis

465
Q
  1. Which of the following statements about the influence of insulin on blood glucose level is wrong:
    a) Insulin reduces the level of blood glucose by accelerating its transport from the blood into insulin-dependent tissues
    b) Insulin stimulates the synthesis of liver and muscle glycogen
    c) Insulin does not stimulate glucose transport in adipose tissue
    d) Insulin stimulates glycolysis in the liver
A

c) Insulin does not stimulate glucose transport in adipose tissue

466
Q
  1. Which of the following statements about the mechanism by which insulin affects the activity of glycogen synthase (regulatory enzyme of glycogenogenesis) is wrong:
    a) insulin decreases the level of cAMP, which leads to dropout of the activation of Protein kinase A, catalyzing the formation of the active phosphorylated form of the protein, called “inhibitor-1”
    b) When the inhibitory protein-1 is inactive (dephosphorylated) it does not inhibit the activity of proteinphosphstase – 1
    c) the active protein phosphatase-1 catalyzes the dephosphorylation of glycogen synthase (glycogen synthase a)
    d) insulin signaling leads to creating of the phosphorylated form of glycogen synthase (glycogen synthase b)
A

d) insulin signaling leads to creating of the phosphorylated form of glycogen synthase (glycogen synthase b)