Energy Storage Flashcards

1
Q

How and where is glycogen stored?

A

As granules in the liver and skeletal muscle

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2
Q

What acts as a primer at the core of glycogen?

A

A dimer of the protein glycogenin

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3
Q

How is glucose converted to glucose-6P?

A

Phosphorylated by ATP using hexokinase

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4
Q

How is glucose-6P converted to glucose-1P?

A

The enzyme phosphoglucomutase

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5
Q

Which enzyme catalyses the reaction between glucose-1P and UTP to produce UDP-glucose?

A

G1P uridylyltransferase

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6
Q

Which enzyme catalyses the reaction between glycogen and UDP-glucose to form a-1-4 bonds?

A

Glycogen synthase

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7
Q

Which enzyme catalyses the reaction between glycogen and UDP-glucose to form a-1-6 bonds?

A

Branching enzyme

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8
Q

Which enzymes reacts glycogen with Pi to release a glucose-1P molecule?

A

Glycogen phosphorylase- a-1-4 bonds

De-branching enzyme- a-1-6 bonds

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9
Q

What is the function of liver glycogen?

A

A buffer of blood glucose levels

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10
Q

What is the purpose of skeletal muscle glycogen?

A

To release glucose-6P to be used in glycolysis

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11
Q

Which enzyme converts glucose-6P into glucose in the liver?

A

Glucose-6-phosphatase

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12
Q

What is the effect of insulin on the activities of glycogen synthase and glycogen phosphorylase?

A

Glycogen synthase activity increase, glycogen phosphorylase activity decrease

Due to de-phosphorylation of enzymes

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13
Q

What is the effect of glucagon/adrenaline on the activities of glycogen synthase and glycogen phosphorylase?

A

Glycogen synthase activity decrease, glycogen phosphorylase activity increase

Due to phosphorylation of enzymes

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14
Q

What is the origin of glycogen storage diseases?

A

They are inherited

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15
Q

What enzyme deficiency causes von Gierke’s disease?

A

Glucose 6-phosphatase deficiency

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16
Q

What enzyme deficiency causes McArdle disease?

A

Muscle glycogen phosphorylase deficiency

17
Q

What are the three major precursors for gluconeogenesis?

A

Lactate, glycerol and amino acids

18
Q

Why can acetylCoA not be converted to pyruvate?

A

The pyruvate dehydrogenase reaction is irreversible

19
Q

Which enzyme phosphorylates oxaloacetate to phosphoenolpyruvate?

A

PEPCK

20
Q

Which enzyme catalyses the dephosphorylation of fructose 1,6- bisphosphate?

A

Fructose 1,6- bisphosphatase

21
Q

Which enzyme converts acetylCoA to malonylCoA?

A

AcetylCoA carboxylase

22
Q

What is required for the fatty acid synthase complex?

A

Malonyl-CoA

ATP

NADPH

23
Q

Which enzyme hydrolyses triacylglycerol to glycerol and free fatty acids?

A

Hormone sensitive lipase