Exam 2 Lecture 17 Glycogen Metabolism I Flashcards

1
Q

the structure of glycogen is a long chain _ of glucose with branches

A

homopolymer

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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

branched points formed via _ bonds between glucose monomers of separate chains

A

alpha-1,6 glycosidic bonds

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4
Q

_ contain a terminal glucose with a free hydroxyl group at carbon 4

A

non-reducing ends (multiple)

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5
Q

_ consists of glucose monomer connected to a protein called glycogenin

A

reducing ends

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6
Q

glycogen is _ and _ from non-reducing ends

A

degraded and extended

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7
Q

glycogen is stored in:

A

liver, muscle, and other tissue

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8
Q

glycogen is stored as _

A

granules

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9
Q

granules contain not only glycogen but also the _ needed for glycogen metabolism

A

enzymes needed for glycogen metabolism

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10
Q

defects in glycogen enzymes can lead to disorders termed _

A

glycogen storage disorders

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11
Q

liver glycogen regulates

A

blood glucose levels (sensor)

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12
Q

muscle glycogen provides

A

reservoir of fuel (glucose) or physical activity

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13
Q

T/F: glycogen metabolism is regulated storage and release of glucose

A

true

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14
Q

T/F: glycogen metabolism synthesis and degradation of glycogen involve the same pathways

A

false; synthesis and degradation are INDEPENDENT of each other

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15
Q

Pathways in glycogen metabolism are regulated independently?

A

yes

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16
Q

how does muscle glycogen supply energy

A

breaks down glycogen and keeps glucose in the muscle to use for activity

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17
Q

what are the ways to regulate glycogen metabolism?

A
  1. allosteric control
  2. covalent modification
  3. hormonal control
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18
Q

how does allosteric control regulate glycogen metabolism

A

want to control enzyme to influence the activity of the enzyme (induces conformation change)

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19
Q

how does covalent modification regulate glycogen metabolism

A

mainly through phosphorylation; reversible

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20
Q

how do hormones regulate glycogen metabolism

A

insulin stimulates phosphatase, glucagon stimulates a kinase (PKA) ie hormones control covalent modifications

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21
Q

What are the 3 key steps to glycogenesis

A
  1. trapping and activation of glucose
  2. elongation of a glycogen primer
  3. branching of glycogen chains
22
Q

how does trapping of glucose occur?

A

glucokinase/hexokinase in cytosol of hepatocytes and muscle cells catalyze phosphorylation of glucose into glucose-6-ohosphate

23
Q

hows does activation of glucose occur?

A

phosphoglucomutase then reversibly isomerizes glucose-6-phosphate into glucose-1-phosphate. UDP-glucose pyrophosphorylase then transfers glucose-1P tp UTP which generates UDP-glucose (active form of glucose)

24
Q

UDP is for _

A

synthesis

25
Q

how does elongation occur?

A

elongation via glycogen synthase (rate limiting enzyme). Have a existing glycogen primer and glycogen synthase catalyzes transfer of glucose from UDP-glucose to non-reducing end of glycogen chain

26
Q

glycogen synthase forms _ glycosidic bonds between glucose molecules

A

alpha-1,4

27
Q

how does branching of glycogen chains occur?

A

when a glycogen chain reaches about 11 residues, a fragment of the chain (about 7 residues long) is broken off at an alpha-1,4 link and reattached elsewhere

28
Q

in branching, an alpha-1,4 link is broken off and attached through an _ link

A

alpha-1,6 link

29
Q

what enzyme is used for branching?

A

glucosyl (4:6) transferase

30
Q

Branching increases _

A

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

31
Q

glycogen degradation aka

A

glycogenolysis

32
Q

glycogen broken down to release _

A

glucose-1-phosphate (rate limiting step)

33
Q

_ remodeled to permit further degradation

A

glycogen remnant

34
Q

in glycogenolysis, glucose-1-phosphate converted to

A

glucose-6-phosphate

35
Q

glucose-6-phosphate from glycogenolysis can now enter various pathways which are:

A
  1. glycolysis
  2. free glucose for release into blood stream
  3. pentose phosphate pathway-NADPH and ribose derivative (nucleic acid synthesis)
36
Q

how many key enzymes for glycogenolysis?

A

4

37
Q

what is the rate limiting enzyme in chain shortening

A

glycogen phosphorylase (GP) catalyzes the cleavage of glycogen

38
Q

chain shortening occurs at the _ end of the polymer

A

non-reducing end

39
Q

GP adds an _ and releases a glucose residue as glucose-1-phosphate

A

orthophosphate

40
Q

GP uses _ as a cofactor

A

pyridoxal phosphate (Vit B6)

41
Q

phosphorolysis of glucose residues continues until the GP gets within _

A

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

42
Q

what does the phosphoglucomutase step do and how does it work?

A

mutase removes phosphate from the 1 position to the 6 position ie converts glucose-1P to glucose-6P. Adds the phosphate to position 6 first then removes phosphate from position 1

43
Q

in branch transfer, the enzyme _ transfers a block of 3 of the remaining 4 glucose to the non-reducing end of the main chain forming an alpha-1,4 bond

A

transferase

44
Q

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

A

alpha-1,6 glucosidase

45
Q

in release of glucose, glucose is phosphorylated by _

A

hexokinase

46
Q

together, transferase and alpha-1,6 glucosidase convert _ glycogen into a _ structure for further action by GP

A

convert branched glycogen into a linear structure

47
Q

in debranching, _ cuts at non-reducing end

A

phosphorylase

48
Q

in debranching of glycogen, yields _ G1P to 1G

A

10 G1P to 1G

49
Q

T/F: glucose-6P cannot get out of the cell

A

true

50
Q

only _ has glucose-6-phosphatase (present in the ER)

A

liver

51
Q

muscle cells do not have glucose-6-phosphatase so _ stays

A

glucose-6P

52
Q

small amount of glycogenolysis via _

A

lysosomal alpha-1,6 glucosidase (acid maltase)