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MHS-Unit 4 > Degradation of Amino Acids 2: The Fate of the Carbon Core > Flashcards

Degradation of Amino Acids 2: The Fate of the Carbon Core Flashcards

1
Q

Fate of carbon core of amino acids

A
  1. Fed: energy resources
    • Glycogen, TAG
  2. Fasting: energy production
    • Co2
    • Pyr
    • TCA intmd.
    • Acetyl CoA, acetoacetate
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2
Q

Degdation of amino acids

A
  • Glucogenic AA → TCA intmd or PYR →LIVERGlucose
  • Ketogenic AA → Acetoacetate or Acetyl CoA →LIVER KB
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3
Q

Conditionally essential AA

A

The sulphur of cysteine comes from methionine

Tyrosine is produced from phenylalanine

Arginine is not essential for adults, but it is essential for children

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4
Q

Outline of synthesis of non-essential AA

  • Core of non-essential aa (10)
  • Tyrosine (1)
A

The carbon cores of 10 non-essential amino acids derive from glucose.

Tyrosine is produced by the hydroxylation of phenylalanine

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5
Q

Coenzymes in amino acid metabolism

transamination & deamination

A

Pyridoxal-Phosphate (B6)

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6
Q

Coenzymes in amino acid metabolism

Methionine metabolism

A

Cobalamins (B12)

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7
Q

Coenzymes in amino acid metabolism

Hydrxylation of phenylalanine, tyrosine and tryptophan

A

Tetrahydrobiopterin

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8
Q

Coenzymes in amino acid metabolism

Oxidative decarboxylation of BCAA

A

Thiamine-Pyrophosphate (B1)

and

Lipoate

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9
Q

Antileukemic drug

A

Asparginase

Asn is required for the growth of fast dividing cells.

  1. Asn A→ Asp B→ OXA
    • (AsparginaseA , ASTB )
    • Recall: AST converts 2-ketoglutrate to Glu, and Asp to OXA)
  2. Asp → Purines and pyrimidines → RNA/ DNA (of fast dividing leukemic cells.
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10
Q

AA’s that are degraded to a-ketoglutarate (aKGlu)

A

Glu, Gln, Pro, Arg, His

Gln → Glu ⇔ aKGlu

Arg → Ornithine ⇔ Glu semialdehyde → Glu ⇔ aKGlu

Proline → Glu semialdehyde → Glu ⇔ aKGlu

Histidine → FIGLu → Glu ⇔ aKGlu

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11
Q

FIGlu levels (urine)

Pts with follic acid deficiency

A

Patients with folic acid deficiency excrete increased amounts of FIGlu in their urine.

FIGlu excretion is used to monitor folic acid deficiency

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12
Q

Histidinemia

Biomarkers Blood and urine

Hint (histidine metabolism)

A

Deficiency in histidase (an enzyme for histidine metabolism)

Biomarker: Elevated levels of histidine in both blood and urine

His A→ Urocanic acid →→ FIGlu THF→ Glu→ a-Ketoglutarate

A - Histidase

Note: Patients with folic acid deficiency (tetrahydrofolate) excrete increased amounts of FIGlu in their urine

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13
Q

Histamine synthesis

rxn

Enzyne

A

Histidine Histidine Decarboxylase→ Histamine + CO2

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14
Q

AA that are degraded to pyruvate

A

Thr → Gly ⇔ Ser → Cys→ pyruvate ⇔ Ala

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15
Q

purines, creatine, heme and gluthathione all are synthesized from this amino acid as precursor

A

Gly

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16
Q

Primary rxn that produces glycine in the brain is synthesized by this enzyme

A

Serine hydrozymethyl transferase

Serine + THF Serine hydroxymethyl Transferase ⇔ Glycine

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17
Q

AA that are degraded to fumarate

A

Phenylalanine → Tyrosine →→→ Malylacetoacetate→ Fumarylacetoacetate

Fumarylacetoacetate → fumarate + acetoacetate

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18
Q

Tyrosinemia Type I

Deficient enzyme

Biomarkers

Spc. characteristics

Liver and kidney status

Tx

A

Fumarylacetoacetate(FAA) X→ fumarate + acetoacetate

deficiency of. fumaryl acetoacetate hydrolase

Accumulation of FAA and succinyl acetone in urine

Cabage like odor

Liver failure

Renal tubular acidosis

Tx: diet restriction of phenyl alanine and tyrosine

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19
Q

Alkaptonuria

A

Disease of the tyrosine degradation pathway.

Due to homogentisic acid oxidase deficiency.

Homogentisic acid accumulates in urine and tissues

Homogentisic acid accumulation in cartilage causes crippling arthritis (dense black deposits).

Urine turns dark within minutes

Scalera bluish-black pigment (generally the first sign) and in the cartilage of the ear.

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20
Q

Oculocutaneous Albinism Type 1

A
  • Due to tyrosinase deficiency
  • White skin, white hair, pink eyes
  • Eye and skin sensitive to sunlight
  • Nystagmus, far or near-sightedness
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21
Q

Biologically important metabolites of Tyrosine

A
  • Melanin (req. tyrosinase)
  • Catecholamine (req. tyrosine hydroxylase and BH4)
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22
Q

PKU

Causes

Tx

A

Deficient phenylalanine hydroxylase

Mutations in the enzyme

Insufficient tetrahydrobiopterin (BH4)

Treatment: Phe-restricted, Tyr supplemented diet

Avoid aspartame, artificial sweetener

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23
Q

PKU Sx

A
  • Elevated phenylalanine, phenylpyruvate, phenyllactate and phenylacetate in blood and urine (musty odor of urine).
  • Neurological problems (mental retardation,seizures, tremors, microcephaly etc) due to reduced production of catecholamines.
  • Hypopigmentation (light skin, hair, blue eyes) due to reduced melanin production.
24
Q

The role of tetrahydrobiopterin in neurotransmitter synthesis

Severity of its deficiency

A

Necessary for hydroxylation of:

  • Phenylalanine (tyrosine production)
  • Tyrosine (first step of catecholamine synthesis)
  • Tryptophan (first step of serotonin and melatonin synthesis)

Note: BH4 deficiency causes more severe phenylketonuria than mutations in phenylalanine hydroxylase

25
Q

Amino acids that are degraded to Succinyl CoA

A

Methionine, threonine, valine and isoleucin

26
Q

A- Brief summary of the rxn of aa degredation to succinyl CoA, and indicate how each of the following aas feed into it

  1. methionine
  2. threonine
  3. valine
  4. isoleucin

B- List the diseases that might occur along these pathways

A

a-KGlu→ propionyl CoA →methylmalonyl CoA→ Succinyl CoA

  1. methionine ⇒ a-Kglu
  2. threonine → a-KGlu
  3. Valine ⇒methylmalonyl semialdehyde →Priopionyl CoA
  4. isoleucine⇒ methylmalonyl semialdehyde →Priopionyl CoA

B- Organic acidimia, which leads to secondary hyperammonemia

  • methylmalonic acidemia
  • propionic acidemia
27
Q

Diseases associated with the following pathway

aa degradation to succinyl CoA

A

Organic acidemia (general term) → 2ndhyperammonemia

Methylmalonic acidemia and priopionic acidemia

28
Q

Causes of the following conditions:

  1. methylmalonic acidemia
  2. propionic acidemia
A

Propionyl CoA <strong>Carboxylase-Biotin</strong> → → methylmalonyl CoA Mutase B12→ Succinyl CoA

  1. Priopionyl CoA carboxylase deficiency
  2. Methylmalonyl CoA mutase deficiency
29
Q

Priopionyl CoA carboxylase deficiency

A

priopionic acidemia (aa degdatation to succinyl CoA)

Organic acidemia due to elevated levels of 3-OH propionic acid

Organic acidimia leads to secondary hyperammonemia

30
Q

Methylmalonyl CoA mutase deficiency

A

methylmalonic acidemia (aa degdradation to succiny CoA)

elevated levels of methylmalony acid in blood

31
Q

Methionine metabolism

Homocystine Formation

A

S-Adenosylmethionine (SAM) is the primary methyl donor in the human body.

It participates in the synthesis of:

  • phosphatidylcholine (cell membrane lipid)
  • creatine (muscle energy metabolism)
  • carnitine (fatty acid degradation)
  • melatonin (sleep-wake hormone)
  • epinephrine (“flight and fright” hormone)
32
Q

The biosynthetic reactions that rely on S-adenosylmethionine as primary methyl donor

A
  • phosphatidylcholine (cell membrane lipid)
  • creatine (muscle energy metabolism)
  • carnitine (fatty acid degradation)
  • melatonin (sleep-wake hormone)
  • epinephrine (“flight and fright” hormone)
33
Q

Methionine metabolism : formation of homocysteine

Rxn

A

L-methionin → SAM→ SA-homocystine → homocystine

SAM: S-Adenosyl Methionione

SA: S-adenosyl

34
Q

Homocystinuria management:

A

Homocystinuria management: Restrict methionine, supplement cysteine

35
Q

Methionine metabolism: degradation of homocystine

Name 2 key enzymes and diseases assoicated with their dificiencies

A

Homocystine Cistathione Synthase→Cystathionine <strong>Cystathionase</strong>→ Cistine

  • Cistathione synthase deficiency- Cyctathioninuria
    • elevated U. homocystine
    • elevated bld. methionina
  • Cystathionase dificiency- homocystinuria
    • elevated cystathionine
36
Q

High level of bld homocysteine is a risk factor for

A

myocardial infarction

37
Q

The cofactors required for transsulfuration rxns that lead to cystine formation (from homocystine)

Hint: methionine degradation

A

pyridoxine- B6

38
Q

Methionine metabolism : degradation of homocysteine

What are the requirement for remethylation rxns?

  • Cofactor
  • Coenzyme
A

Cofactor: folate

Coenzymes: B12 derived coenzymes

39
Q

BCAA

determine ketogenic or glucogenic

A

Valine, Isoleucin and leucin

  1. Valine- Glucogenic
  2. Isoleucine- Glucogenic and ketogenic
  3. Leucine- Ketogenic
40
Q

rxn type that is catalyzed by a-ketoacid dehydrogenase

A

oxidative decarboxylation

41
Q

Factors required for proper functioning of a-ketoacid dehydrogenase

(BCAA metabolism)

A

Just like Pyruvate dehydrogenase complexes (PDH) it requires 5 cofactos:

  1. TPP
  2. lipoate
  3. FAD
  4. NAD
  5. CoASH

a-ketoacid dehydrogenase participate in oxidative decarboxylation reactions.

42
Q

The first and second reactions of BCAA metabolism

Reactants

Products

Enzymes and their cofactors

The end products made from each BCAA

A

BCAA Transamination⇔ a-ketoacid a-ketoacid dehydrogenase⇒ X-CoA + CO2 + NADH

a-ketoacid dehydrogenase req. TPP, Lipoate, NAD, FAD, CoASH

Valine (Glucogenic) metabolism ► succinyl CoA

Leucine (Ketogenic) metaboliosm ► acetoacetate and acetyl CoA

Isoleucine ( ketogenic and glucogenic) ►acetyl CoA and succinyl CoA

43
Q

Maple syrup urine disease (MSUD)

I Love Vermont Maple Syrup

  • Dx
  • Sx
  • Tx
A

Dx

Elevated BCAAs, especially leucine, in blood.

Elevated branched-chain ketoacids (BCKA) in blood and especially in urine.

Sx:

Maple syrup odor of urine (by 5-7 days after birth) and of earwax (12-24 hr after birth).

Encephalopathy (lethargy, poor feeding, apnea, opisthotonus, coma)

BCAA restricted high calorie diet. Usually BCAA-free formulas, supplemented with limited amounts BCAAs. Leucine is always the most restricted.

All BCAAs are essential amino acids.

44
Q

MSUD Tx

A

BCAA restricted high calorie diet. Usually BCAA-free formulas, supplemented with limited amounts BCAAs. Leucine is always the most restricted.

BCAAs are essential.

45
Q

Pellagra

Causes and manifestation

A

Lack of tryptophan and niacin (vitamin B3) in diet causes pellagra (characterized by the 4 Ds – Dermatitis, Diarrhea, Dementia and if untreated Death).

46
Q

Tryptophan metabolism

A

Lack of tryptophan and niacin (vitamin B3) in diet causes pellagra (characterized by the 4 Ds – Dermatitis, Diarrhea, Dementia and if untreated Death).

47
Q

Diseases of AA metabolism

General Concepts

A

vRare diseases

(incidence is generally less than 1:2,000).

Can be caused by -

  • Mutated enzymes (autosomal recessive).
  • Insufficient co-factors.

Many have neurological symptoms.

AAs are precursors of neurotransmitters and hormones

Early detection and treatment is a must!!!

Many require dietary adjustment in protein consumption.

48
Q

ketogenic family of amino acids

A

WIFY LK

WIFY are both ketogenic and glucogenic

LK only ketogenic

W- Trp

I- Ile

F- Phe

Y- Tyrosine

L- Leucin

K- Lysine

49
Q

Amino acids that are both ketogenic and glucogenic

A

WIFY

Trp-Ile, Phe, Tyr

50
Q

Acetyl Coa Family of aa

(based on the point where their C skeleton enter the TCA cycle)

Determine the essential aa’s

A

W*I*F*YL*K*

W-Trp (essential)

I-Ile (essential)

F-Phe (essential)

Y-Tyr

L-Leu (essential)

K- Lys (essential)

51
Q

a- Ketoglutrate family of aa

(based on the point where their C skeleton enter the TCA cycle)

A

_H<span>*</span>_Q REP

H-His (essential)

Q- Gln (Glutamine)

R- Arg

E- Glu (Glutamate)

P-Proline

52
Q

Succinyl CoA Family of AA

(based on the point where their C skeleton enter the TCA cycle)

A

VIM

Val (essential)

Ile (essential)

Met (essential)

53
Q

Fumarate Family of Amino Acids

(based on the point where their C skeleton enter the TCA cycle)

A

FY

F-Phe

Y-Tyr

54
Q

Oxaloacetate Family of AA

(based on the point where their C skeleton enter the TCA cycle)

A

ND

Asn- N

Asp- D

55
Q

Pyruvate Family of AA

(based on the point where their C skeleton enter the TCA cycle)

A

CAST GW

Cys- Ala- Ser-_Thr*-Gly-_Trp*

Thr and Trp are essential aa.

56
Q

rxn fascilitated by the methyl group of Met

A

methylation reactions as S-adenosylmethionine

SAM

Met SAM Synthetase→ SAM Methyl Transferase→ SAH

MHS-Unit 4 (11 decks)

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