Quiz 3 Glycogen Synthesis (Glycogenesis) Flashcards

1
Q

What acts faster when glucose is needed, Glycogenolysis or GNG?

A

Glycogenolysis

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2
Q

Two primary storage sites of glycogen?

A

Liver and skeletal muscle

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3
Q

For review…a branch occurs how many glucose apart? What type of bond?

A

10 glucose molecules…A(1-6) bond

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4
Q

Muscle or liver lack enzyme to release glucose? What enzyme?

A

Muscle, glucose-6-phosphatase

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5
Q

Glycogenesis is initiated by?

A

Glucose-6-phosphate

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6
Q

If no glycogen fragment available, what begins the glycogen chain?

A

Glycogenin

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7
Q

Enzyme which starts the glycogen chain with amino acid tyrosine

A

Glycogen initiator synthase

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8
Q

How many ATP used to make glucose-6-phosphate?

A

1

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9
Q

Reactants of Phosphoglucomutase?

A

Glucose-6-phosphate

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10
Q

Products of Phosphoglucomutase?

A

Glucose-1-phosphate

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11
Q

What breaks apart pyrophosphate when making UDP-glucose?

A

Pyrophosphatase

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12
Q

What high energy compound is used to make UDP-Glucose?

A

UTP (uridine triphosphate)

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13
Q

What are the reactants of UDP-glucose Pyrophosphorylase?

A

UTP + Glucose-1-phosphate

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14
Q

What are the products of UDP-glucose Pyrophosphorylase?

A

PPi + UDP-Glucose

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15
Q

How many high energy molecules are used to synethsize glycogen?

A

3

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16
Q

What occurs during chain elongation? Where is this taking place in the cell?

A

Glucose is being added to chain, occurs in the CYTOSOL.

17
Q

What enzyme is involved with Chain elongation? What types of bonds are being made?

A

Glycogen synthase, alpha (1-4) bonds

18
Q

After ~ how many glucose added to the chain do we need to begin to branch?

A

7 (do not confuse this with the question earlier about how many glucose are in row until we find a branch which is 10)

19
Q

Which enzyme is involved with branching and alpha (1-6) bonds?

A

Glycosyl-(4:6)-transferase

20
Q

What is the key enzyme responsible for synthesis of glycogen?

A

Glycogen synthase

21
Q

Allosteric regulation of glycogen synthase would be activated by?

A

glucose-6-phosphate

22
Q

During exercise, is glycogenolysis or glycogenesis being active?

A

During exercise glycogenolysis (breakdown), and post exercise glycogenesis (synthesis)

23
Q

If you phosphorylate glycogen synthase (hormonal regulation), will be it be active or inactive?

A

Inactive

24
Q

Give examples of things that will inactivate glycogen synthase?

A

Glucagon, Epinephrine, norepinephrine

25
Q

What will de-phosphorylate and active the enzyme?

A

Insulin

26
Q

In other words, Glucagon would inhibit what and stimulate what?

A

Inhibit glycogen synthesis and stimulate glycogen breakdown

27
Q

High ATP, High levels of glucose, Insulin, and low glycogen levels do what to glycogen synthase?

A

Stimulate

28
Q

Primary site of fructose disposal?

A

liver

29
Q

What are the two enzymes essential for fructose metabolism highly expressed in the liver?

A

Fructokinase, and Triokinase

30
Q

Low-dose fructose causes what?

A

A threefold increase in net liver glycogen synthesis

31
Q

Does fructose benefit muscle glycogen synthesis?

A

NOPE only live glycogen synthesis.

32
Q

After intense exercise, glycogen synthesis happens at initially a high rate, it rapidly declines to about a 1/5th by 60 minutes and a 1/9th by 120 minutes. What are the two reasons for this?

A

Increased glucose uptake (GLUT 4) and increased enzyme activity (glycogen synthase)

33
Q

What phase of glycogen synthesis is 30-60 mins after exercise and is insulin independent?

A

Rapid phase

34
Q

After rapid phase, insulin dependent, and has a much slower rate of glycogen synthesis?

A

Slow phase

35
Q

True or false, by increasing carb consumption, does it increase the rate of glycogen storage by more than 150%?

A

True

36
Q

Incorporating ingestion of what along with moderate intake of carbs leads to higher muscle glycogen synthesis rates?

A

Proteins/amino acids

37
Q

When enzymes of glycogen degradation or glycogen synthesis are defective and leads to increased storage but impaired breakdown?

A

Glycogen storage disease (GSD)

38
Q

Most common GSD, is genetic, glucose – phosphatase deficiency (hypoglycemia)?

A

GSD type 1 or Von Gierk’s disease