Carbohydrates and Glycogen Metabolism Flashcards

1
Q

What is the difference between Epimers and Enantiomers?

A
Epimers: Isomer that differ in
configuration only one carbon atom
Enantiomers: The groups attached to the
asymmetric carbon atom can be
arranged to form two different isomers
that are mirror images of each other
are not superimposable.
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2
Q

Which is of the following is true?
A. The new stereocenter of the cyclic form is referred to as the anomeric carbon.
B. If the OH group on the anomeric carbon is axial DOWN, anomeric carbon is α
C. In solution, OH group on the anomeric carbon spontaneously changes from α to β position through a process called mutarotation
D. If the OH group on the anomeric carbon is equatorial up, anomeric carbon is β
E. All

A

E

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3
Q

Which of the following is wrong?
A. If the anomeric carbon is not linked to another molecule, the ring can open and sugar act as a reducing sugar.
B. All monosaccharides are reducing sugar
C. 1,6 glycosidic bonds forms linear, 1,4 glycosidic bonds forms branched poly saccharides
D. Sucrose is a non reducing sugar while maltose and lactose are reducing sugar.

A

C
1,4 - linear
1,6 - branched

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4
Q

Which of the following enzyme is correctly matched with its function
A. glycoside hydrolases (glycosidases) hydrolyze glycosidic bonds in poly-and oligo-saccharides
B. Glycogen Synthase makes α(1-4) glycosidic bonds using a fragment of glycogen as primer
C. Disaccharidases hydrolyze tri-and
di-saccharides into their reducing sugars.
D. All
E. None

A

D

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5
Q

Wat is the most common digestive enzyme deficiency?

A

Lactose intolerance

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6
Q

The glycogen is degraded to glucose by the process of…………..

A

glycogenolysis

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7
Q

Which of the following is False?
A. When there is excess of glucose, it is used to synthesize glycogen in a process called glycogenesis.
B. specific tissues synthesize glucose de novo, using amino acids from the body’s proteins as primary source of carbons via gluconeogenesis.
C. Gluconeogenesis is a slow process
D. Dietary glucose is a constant source of energy for the human body
E. None

A

D

Dietary glucose is not always constant source

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8
Q

Glycogen has……
A. only one anomeric carbon
B. Reducing end attached to the protein glycogenin by glycosidic bond.
C. 1/3 of glycogen is water
D. Branches occur more frequently in the center
E. A and B
F. All except C

A

F

2/3 of glycogen is water

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9
Q

Which of the following is true about glycogen storage?
A. Glycogen gets broken to Glucose6-P and never leaves the muscle cell.
B. 400 g of glycogen is stored in liver while 100g is stored in muscle.
C. Muscle glycogen is not affected by short periods of fasting time while Liver glycogen can maintain blood glucose only for 18 h.
D. Pyruvate and lactate are produced in the liver
E. A and C
F. B and C

A

E
400g- muscle
100g- liver
Pyruvate and lactate are produced in muscle

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10
Q

Why body store most of energy in the form of adipose tissue not as glycogen?

A
  1. fats are hydrophobic so they take less place than glycogen
  2. fats have high ATP production so they are only used for emergencies.
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11
Q

Choose the correct one
I. In order glycogen to be synthesized, glucose has to be linked to high energy molecule, UDP. (UDP-glucose pyrophosphorylase)
II. In the absence of glycogen synthase, protein called glycogene serves as an acceptor of glucose.
III. Branches are made by
branching enzyme amylo- α(1-6) -> α(1-4)
transglucosidase
IV. Glycogen Synthase makes α(1-4) glycosidic bonds using a fragment of glycogen as primer
A. I, II, III B. II, III IV
C. I, III, IV D. I, II, IV

A

D.
Branches are made by
branching enzyme amylo- α(1-4) -> α(1-6)
transglucosidase

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12
Q

Where does Glycogenesis occur?

A

cytosol

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13
Q

What is the purpose of Glycogen

phosphorylase in glycogenolysis?

A

sequentially cleaves the α(1-4) glycosidic

bonds by simply phosphorylation and producing glucose1-phosphate

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14
Q

What is the correct pathway of glycogenolysis?

A

GLYCOGEN- Debranching enzyme- GLUCOSE( small amount)- glycogen phosphorylase- GLUCOSE 1-PHOSPHATE - GLUCOSE 6-PHOSPHATE- glucose 6-phosphotase - GLUCOSE

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15
Q

What is the correct pathway of glycogenesis?

A

GLUCOSE- hexokinase/glucokinase- GLUCOSE 6-PHOSPHATE- phosphoglucomutase- GLUCOSE 1-PHOSPHATE- UDP-glucose pyrophosphorylase- UDP-G- glycogen synthase( branching enzyme) - GLYCOGEN

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16
Q

Which of the following is wrongly matched with its function
A. Insulin’s :increase glucose levels in blood
B. Epinephrine’s :elicit a short term release of glucose from stores
C. Cortisol’s action: to stimulate make of glucose from proteins.
D. Glucagon’s :stimulate the release of
glucose from stored glycogen

A

A
Insulin reduce the level of sugar in blood
Insulin stimulate storage of fuel while the rest stimulate release of fuel.

17
Q

Fill in the blank
In muscle during exercise, After the production of pyruvate from glucose 6-phosphate,
lactate is formed in………….
CO2 is formed in……………..

A

Anerobic (fast)

Aerobic (slow)

18
Q

Which of the following is true
I. In liver, while fasting- glucagon increase
- Insulin decrease
II. In muscle during exercise- Epinephrine
decrease
III. In liver, after meal - glucagon decrease
- Insulin increase
IV. In muscle after meal - insulin increase
V. while fasting - glycogenesis increase
- glycogenolysis decrease
A. I, II, III, B. I, III, IV
C. II, IV, V D. III, IV, V

A

B
In muscle during exercise- Epinephrine
increase
while fasting - glycogenesis decrease
- glycogenolysis increase

19
Q

Glycogen synthase is activated by………..
inhibited by…………
Glycogen phosphorylase is activate by……..
inhibited by……

A

a. insulin and glucose
b. glucagon and epinephrine
c. glucagon and epinephrine, AMP
d. insulin, ATP

20
Q
Which of the following are glycogen storage diseases?
A. Pompe disease
B. Corin disease
C. McArdle syndrome
D. Von Gierke disease
E. All
A

E

21
Q

What are the two basic classification of monosaccharides?

A

Aldose - COH

Ketose - CO