glycogen metabolism Flashcards

1
Q

glycogen

A

glucose storage form in animals and microorganisms
- storage as a polymer avoids a large increase in osmotic pressure
-B- particle contains about 55,000 glucose residues
- 20-40 B particles will cluster together in a a-rosette

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2
Q

what do plants use instead of glycogen?

A

starch

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3
Q

what are the two primary storage organs?

A

muscle and liver

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4
Q

glycogen accounts for about 1-2% of this organ’s mass
- overall stores a higher quantity of glycogen due to its larger mass
stores glycogen for itself
provides a quick energy source for aerobic and anaerobic metabolism

A

muscle

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5
Q

glycogen accounts for about 10% of this organ’s mass
stores glycogen for the whole body

A

liver

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6
Q

glycogen stores are quickly _______

A

depleted; only really enough for 24 hours

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7
Q

remember that even though _____ are able to store more energy, they can’t be converted to glucose in mammals and can’t be catabolized anaerobically.

A

fats

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8
Q

2 monosaccharides can be joined by an O-glycosidic bond to form a disaccharide
- this is a ______________ reaction of an alcohol and a hemiacetal
- they can be separated through ___________

A

condensation; hydrolysis

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9
Q

in sugar polymers, there will be a reducing end and a non-reducing end
- the ___________ will have a free hemiacetal that can still be reduced

A

reducing end
( everything adds to the nonreducing end)

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10
Q

glycogen contains both linear and branched chains
- the linear chain has __________ glycosidic bonds
- the branched chain has __________ glycosidic bonds
branching occurs every 8-12 residues

A

a(1->4)
a(1->6)

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11
Q

branching increases the number of ____________ ends
this is a good thing because it increases ____________ and _______________

A

non-reducing ends; solubility; accessibility

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12
Q

glycogen breakdown (glycogenolysis) step 1

A

enzyme: glycogen phosphorylase
Pi cleaves a (1->4) glycosidic bond on the nonreducing end
- continues until 3 residues away from an a(1->6) glycosidic branch point
- this is a phosphorolysis reaction
some of the bond energy is conserved in phosphate ester formation
enzyme requires pyridoxal phosphate as a cofactor (derivate of vitamin B6)

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13
Q

glycogen breakdown (glycogenolysis) step 2

A

enzyme: debranching enzyme
2 activities of enzyme:
1.) transferase activity
- transfers 3 glucose molecules from the branch to the non-reducing end
2.) a 1->6 activity
- glucose is cleaved and released as free glucose

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14
Q

glycogen breakdown (glycogenolysis) step 3

A

enzyme: phosphoglucomutase
glucose-1-phosphate is converted to glucose-6-phosphate
no energy input needed
reaction is reversible
in muscle, the product can then be used in glycolysis pathway

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15
Q

glycogen breakdown (glycogenolysis) step 4

A

enzyme: glucose-6-phosphetase
enzyme is integral membrane protein of the ER
found in liver and kidneys only
dephosphorylates glucose-6-phosphate to give glucose

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16
Q

glycogen synthesis (glycogenesis)

A

can occur anywhere in the body but it is primarily seen in the liver and skeletal muscles
starting point is glucose-6-phosphate, which is formed from glucose
D-glucose+ATP->D-glucose-6-phosphate+ADP (enzyme: hexokinase I/II for muscle and hexokinase IV/glucokinase for liver)
glucose-6-phosphate=glucose-1-phosphate (enzyme: phosphoglucomutase)

17
Q

glycogenesis step 1

A

enzyme: UDP-glucose phosphorycase
UDP-glucose is a sugar nucleotide (with increased energy for polymerization)
- joined at anomeric carbon
glucose-1-phosphate+UTP-> UDP-glucose+PPi

18
Q

glycogenesis step 2

A

enzyme: glycogen synthase
UDP-glucose to non-reducing end of glycogen residue
- makes a new a(1->4) glycosidic bond
- UDP is eliminated

19
Q

glycogenesis step 3

A

enzyme: glycogen branching enzyme
transfers a fragment from the nonreducing end to the C-6 hydroxy group at a more interior position on the chain
branching increases solubility and accessibility and the number of nonreducing ends

20
Q

regulation of glycogenolysis

A

regulated both allosterically and hormonally
there are two forms of glycogen phosphorylase that are interconvertible
- phosphorylase a is the active form while phosphorylase b is the less active form
conversion occurs when a specific serine residue in phosphorylase b is phosphorylated

21
Q

hormonal control is dependent on energy demand and blood glucose

A

glucagon signals low blood sugar (activates glycogenolysis)
insulin signals high blood sugar
glucagon (liver) and epinephrine (muscles) both activate phosphorylase b kinase
insulin actives phosphorylase a phosphatase (PP1)

22
Q

there are two allosteric control mechanisms

A

Ca2+ binding activates phosphorylase b kinase
- ca2+ signals for muscle contraction (activates glycogenolysis)

AMP binding activates phosphorylase a
- AMP accumulation indicates vigorous muscle contraction
- when ATP levels are sufficient, ATP blocks the allosteric site where AMP binds

23
Q

regulation of glycogenesis

A

there are two forms of glycogen synthase that are interconvertible
- glycogen synthase a is the active form while glycogen synthase b is the less active form

24
Q

phosphorylation of glycogen synthase A

A

phosphorylation of glycogen synthase a converts it to glycogen synthase b
- many different residues can be phosphorylated
- casein kinase II (CKII) does a single phosphorylation which primes it for GSK3
- glycogen synthase kinase 3(GSK3) phosphorylates three serine residues near the carboxyl terminus
- PKA mediates the action of glucagon (liver) and epinephrine (muscle) and phosphorylates glycogen synthase a to inactivate the enzyme by covalent modification

25
Q

dephosphorylation of glycogen synthase B

A

converts it to glycogen synthase a
- promoted by PPI

Insulin stimulates glycogen synthesis by activation PPI