glycogen synthesis Flashcards

1
Q

what is the function of liver glycogen?

A

used to maintain glucose levels in the blood

stores glucose when glucose levels are too high and releases glucose when glucose levels are too low

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2
Q

what is the function of muscle glycogen?

A

maintain muscle during bursts of activity

local energy store to allow muscles to do their first burst of energy

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3
Q

what is the advantage of glycogen being less osmotically active than glucose?

A

can be stored

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4
Q

why can liver glycogen be used to make glucose and not muscle glycogen?

A

liver has an enzyme which isn’t found in muscle tissue which allows glucose-6-phosphate to be dephosphorylated back to glucose

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5
Q

in what ways can muscle glycogen be used to make ATP?

A

anaerobic glycolysis

aerobic metabolism

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6
Q

what is glycogenic?

A

a protein primer

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7
Q

which bonds join molecules of glucose together in glycogen?

A

carbon 1-4 links

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8
Q

which end of glycogen is extended?

A

carbon 4 end

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9
Q

which bond is needed to form a branch in glycogen?

A

carbon 1-6

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10
Q

what enzyme is needed to form a glycogen branch?

A

glycogen branching enzyme

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11
Q

after how many residues is a branch found in the main chain of glycogen?

A

every 12-14 residues

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12
Q

what is the advantage of branches?

A

make glycogen and its energy easily accessible

helps solubility inside cell

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13
Q

explain the process of glycogen synthesis

A

glucose-6-phosphate –> glucose-1-phosphate

UTP used to make UDP-glucose and PPi

Glycogen synthase removes UDP and adds glycogen onto the glycogen chain to extend it, with glycogenin as the primer

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14
Q

how is glucose-6-phosphate converted into glucose-1-phosphate?

A

moving the phosphate from carbon 6 to carbon 1

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15
Q

what is the energy from PPi –> 2Pi used for?

A

pushing UDP-glucose–> glycogen reaction to the right

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16
Q

what effect does insulin have on glycogen synthase and glycogen?

A

insulin increases glucose storage into glycogen

glycogen synthase is active

17
Q

what effect does glucagon have on glycogen synthase and glycogen?

A

glucagon releases glucose into the blood

glycogen synthase is inactive

18
Q

how is glycogen synthase affected when it’s phosphorylated/dephosphorylated?

A

Phosphorylated – inactive

Dephosphorylated – active

19
Q

how does insulin dephosphorylate glycogen synthase?

A

activating protein phosphatase-1

20
Q

how is glycogen synthase phosphorylated?

A

protein kinase A and phosphorylase kinase

21
Q

what controls the phosphorylation of glycogen synthase?

A

cAMP
glucagon (liver)
adrenaline (muscle)

22
Q

what is glycogenolysis?

A

breakdown of glycogen

23
Q

what stimulates the breakdown of liver glycogen?

A

glucagon via phosphorylation of glycogen phosphorylase

24
Q

what enzyme breaks down glycogen?

A

glycogen phosphorylase

25
Q

what effect does phosphorylation and dephosphorylation have on glycogen phosphorylase?

A

Phosphorylated – active

Dephosphorylated – inactive

26
Q

what enzyme converts glucose-6-phosphate to glucose?

A

glucose-6-phosphatase

27
Q

what does muscle glycogen breakdown feed into?

A

glycolysis and energy production in that cell only

28
Q

under anaerobic conditions, what does glycolysis produce?

A

lactate

29
Q

describe the control of glycogen breakdown

A

Adrenaline + Glucagon activates adenylyl cyclase to convert ATP to cAMP
cAMP activates Protein Kinase A (PKA) to convert ATP to ADP.
phosphorylase kinase b into phosphorylase kinase a which then converts ATP to ADP
used to convert glycogen phosphorylase b to glycogen phosphorylase a
Glycogen phosphorylase cleaves glycogen to produce glucose-1-phosphate
then converted to glucose-6-phosphate

30
Q

what inheritance pattern are all glycogen storage diseases?

A

autosomal recessive

31
Q

what is the deficiency and consequence of type 1 - von Gierke’s?

A

glucose-6-phosphatase deficiency

leads to hypoglycaemia and lacticacidemina

32
Q

what is the deficiency and consequence of type 2 (Pompe’s)?

A

deficiency in lysosomal glycogen breakdown

leads to heart failure

33
Q

what is the deficiency and consequence of type 3 (Cori’s)?

A

deficiency in debranching enzyme

leads to hypoglycaemia

34
Q

what is the deficiency and consequence of type 4 (Andersen’s)?

A

deficiency in branching enzyme

unknown consequence

35
Q

what is the deficiency and consequence of type 5 (McArdle’s)?

A

deficiency in muscle phosphorylase

leads to exercise-induced cramps and fatigue

36
Q

what is the deficiency and consequence of type 6 (Her’s)

A

deficiency in liver phosphorylase

leads to hypoglycemia