Metabolic pathways Glycogen Flashcards

1
Q

What is glycogen?

A

Main storage form of glucose in liver and muscle

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2
Q

What are the differences in storage of liver and muscle glycogen?

A

Liver- Glucose broken down is released to the red blood cells, Brain etc

Muscle- Glucose broken down can only supply that muscle

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3
Q

What is Glycogenesis?

A

Synthesis of glycogen from glucose

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4
Q

What is Glycogenolysis?

A

Glycogen breakdown releasing glucose

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5
Q

Glycogenolysis peaks during non meal times. T/F?

A

True

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6
Q

How is glucose derived overnight during sleep?

A

By gluconeogeneis- glucose produced by breaking down non carbohydrates

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7
Q

Glycogen is a polymer made from glucose monomers joined by what type of bonds?

A

a-1,4 glycosidic

Branches- a1,6 glycosidic bonds

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8
Q

Why is glycogenin important?

A

Glycogenin- attaches 4 glucose molecules together

Provides a primer which can be used to add/ remove glucose molecules to form or breakdown glycogen

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9
Q

Glucose is directly converted to glycogen. T/F?

A

False.

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10
Q

What are the steps of glucose conversion to glycogen? (4)

A
  1. Glucose–> glucose-6-phosphate
  2. Glucose-6-phosphate–>Glucose-1-phosphate
  3. Glucose 1 phosphate–> UDP glucose
  4. UDP glucose + (glucose)n+1 –> Glycogen
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11
Q

What important enzyme controls the process of adding glucose to UDP glucose to form glycogen?

A

Glycogen synthase (rate limiting enzyme)

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12
Q

Whys is UDP glucose important?

A

Activated form of glucose, allows glucose to be added to glycogen at the end of its chain

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13
Q

What enzyme introduces the branches of glycogen formed by a1,6 glycosidic bonds?

A

Transglycosylase

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14
Q

Which enzyme catalyses glycogenolysis?

A

Glycogen phosphorylase (rate limting enzyme)

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15
Q

Action of glycogen phosphorylase?

A

Adds phosphate to glycogen

Produces glycogen-1-phosphate

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16
Q

What enzyme converts glucose-1-phosphate to glucose-6-phosphate?

A

Phosphoglucomutase

17
Q

What happens to glucose-6-phosphate in the liver and muscle?

A
  1. Liver- dephosphorylated and glucose produced is used

2. Muscle - Cant be dephosphorylated so enters glycolysis and TCA cycle

18
Q

What happens in glycogen storage disease?

A

Defect in various of the above enzymes causes excessive glycogen storage in liver, muscle or both