glycogen metabolism I Flashcards

1
Q

glycogen

A

long chain homopolymer of glucose molecules with branches

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2
Q

glucose molecules within linear chain linked together via

A

alpha-1,4 glycosidic bonds

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3
Q

branch points between glucose monomers of separate chains are formed via

A

alpha-1,6 glycosidic bonds

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4
Q

non-reducing ends contain

A

a terminal glucose with a free hydroxyl group at carbon 4

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5
Q

reducing end consists of glucose monomer connected to a protein called

A

glycogenin

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6
Q

glycogenin creates a short glycogen polymer on itself and serves as a

A

primer for glycogen synthesis

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7
Q

glycogen is degraded and extended from

A

non-reducing ends

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8
Q

glycogen is stored in

A

liver, muscle, and other tissues

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9
Q

glycogen is stored as

A

granules

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10
Q

granules contain not only glycogen but also

A

the enzymes needed for glycogen metabolism

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11
Q

function of liver glycogen

A

regulates blood glucose levels

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12
Q

function of muscle glycogen

A

provides reservoir of fuel (glucose) for physical activity

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13
Q

regulation of glycogen metabolism

A

allosteric control

covalent modification through reversible phosphorylation of key enzymes

hormonal control

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14
Q

glycogenesis

A

synthesis of glycogen

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15
Q

3 key steps of glycogenesis

A

trapping and activation of glucose

elongation of a glycogen primer

branching of glycogen chains

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16
Q

rate limiting enzyme of glycogenesis

A

glycogen synthase (catalyzes transfer of glucose from UDP-glucose to non-reducing end of glycogen chain)

forms an alpha-1,4 glycosidic bond between glucose molecules

17
Q

when glycogen chain reaches ______ residues, a fragment of the chain (about 7 residues long) is broken off at an alpha-1,4 link and reattached elsewhere through

A

11

alpha-1,6 link by glucosyl (4:6) transferase

18
Q

what does branching achieve

A

increases solubility of glycogen and increases number of terminal non-reducing ends

increases rate at which glycogen can be synthesized and degraded

19
Q

a new branch point must be at least _____ residues away from a preexisting branch

A

4

20
Q

glycogenolysis overview pathway

A

glycogen –> glucose 1-phosphate (via glycogen phosphorylase) –> glucose 6-phosphate (via phophoglucomutase) –> free glucose can enter glycolysis (muscle/brain), free glucose can enter blood (for use by other tissues), or can enter pentose phosphate pathway (resulting in ribose and NADPH)

21
Q

glycogenolysis in liver

A

glycogen –> glucose 1-P (via glycogen phosphorylase with co-factor vitamin B6) (rate limiting step) –> glucose 6-P (via PGM) –> glucose (via glucose 6-phosphatase) –> free glucose released into blood to maintain blood glucose

22
Q

glycogenolysis in muscle

A

glycogen –> glucose 1-P (via glycogen phosphorylase with co-factor vitamin B6) (rate limiting step) –> glucose 6-P (via PGM) –> pyruvate (via glycolysis) –> pyruvate kept in muscle to produce ATP

23
Q

4 key enzymes of glycogenolysis:

A
  1. glycogen phosphorylase (rate limiting step): degrade glycogen to glucose 1-P)
  2. debranching enzyme transferase: transfers a block of 3 of the remaining 4 glucose residues to the non-reducing end of the main chain forming an alpha-1,4 bond
  3. alpha-1,6-glucosidase: cleaves the alpha-1,6 bond of the single remaining glucose residue to release the free glucose
  4. converts glycogen breakdown product suitable for further metabolism (glucose 6-Phosphatase or PGM)????
24
Q

phosphorolysis of glucose residues (via glycogen phosphorylase) continues until GP gets within

A

4 residues of the alpha-1,6 linkage of a branch point

25
Q

glycogen phosphorylase (GP) adds an ________ and releases a glucose residue as ________

A

orthophosphate

glucose 1-P

26
Q

cofactor required for glycogen phosphorylase (GP)

A

pyridoxal phosphate (vitamin B6)

27
Q

phosphoglucomutase

A

converts glucose 1-P to glucose 6-P

28
Q

how does phosphoglucomutase (PGM) work

A

a phosphoryl group is transferred from the enzyme to the substrate, and a different phosphoryl group is transferred back to restore the enzyme to its initial state

29
Q

debranching enzyme transferase

A

transfers a block of 3 of the remaining 4 glucose residues to the non-reducing end of the main chain forming an alpha-1,4 bond

30
Q

debranching enzyme or alpha-1,6-glucosidase

A

cleaves the alpha-1,6 bond of the single remaining glucose residue to release the free glucose

31
Q

glucose 6-Phosphatase is present in ____ cells not in ____ cells

A

liver

muscle

32
Q

small amount of glycogenolysis occurs in lysosome via

A

lysosomal alpha-1,6 glucosidase (acid maltase)

33
Q

defect in acid maltase (lysosomal alpha-1,6 glucosidase)

A

pompe disease

34
Q

glycogenolysis yields ____ glucose 1-P to every ____ free glucose

A

10

1