Energy Storage Flashcards

1
Q

Write the four steps in glycogenesis

A

Glucose + ATP —> G6P + ADP (hexokinase/glucokinase) G6P G1P (phosphoglucomutase) G1P + UTP +H2O —> UDP-glucose + 2Pi Glycogen(n residues) + UDP-glucose —> glycogen(n residues + 1) + UDP (glycogen synthase and branching enzymes)

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2
Q

Write the overall equation for glycogenolysis

A

Glycogen(n residues) + nPi —> 0.9n G6P + 0.1n glucose

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3
Q

Write the three steps in gycogenolysis

A

Glycogen(n) + Pi —> G1P + glycogen(n+1) (glycogen phosphorylase/branching enzymes) G1P G6P (phosphoglucomutase) G6P + H2O —> glucose + Pi

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4
Q

Which bonds do glycogen phosphorylase and de-branching enzymes affect?

A

Glycogen phosphorylase - glycosidic 1,4 bonds - phosphorolysis therefore produces G1P De-branching enzyme - glycosidic 1,6 bonds - produces free glucose

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5
Q

What is the difference between liver and muscle glycogen?

A

Liver - glucose store for all tissues of the body. Muscle - G6P store, only for muscles

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6
Q

Which two main enzymes are used in glycogen metabolism?

A

Glycogen synthase and glycogen phosphorylase

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7
Q

What inhibits glycogen synthase?

A

Phosphorylation (de phosphorylation activates glycogen synthase)

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8
Q

Which three enzyme defects can lead to abnormal glycogen metabolism?

A

Glycogen phosphorylase, phosphoglucomutase and glucose-6-phosphatase (liver)

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9
Q

What is the main site of gluconeogenesis?

A

Liver

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10
Q

What are possible substrates for gluconeogenesis?

A

Pyruvate, lactate and glycerol can be converted to glucose. Essential and non-essential amino acids whose metabolism involves pyruvate.

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11
Q

What is the overall equation for gluconeogenesis?

A

2 pyruvate + 4 ATP + 2 GTP + 2 NADH –> glucose + 2 NAD+ + 4 ADP + 2 GDP + 6Pi + 2H+

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12
Q

What stimulates glycogen phosphorylase?

A

De-phosphorylation (inhibited by phosphorylation)

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13
Q

How are the irreversible steps of glycolysis by-passed in gluconeogenesis?

A

1 & 3 - thermodynamically spontaneous reactions (glucose 6-phosphatase and fructose 1,6-bisphosphatase) 10 - ATP and GTP-driven hydrolysis (pyrivate carboxylase and PEPCK)

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14
Q

What are the major control sites for gluconeogenesis?

A

PEPCK and fructose 1,6-phosphatase

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15
Q

What stimulates PEPCK and fructose 1,6-phosphatase?

A

High glucagon, low insulin therefore insulin:anti-insulin ratio is important

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16
Q

How are TAGs usually stored?

A

In an anhydrous form in adipose.

17
Q

What is the function of TAGs?

A

Store of fuel molecules for prolonged aerobic exercise.

18
Q

How is storage of TAGs controlled?

A

Hormonally: promoted by insulin, depletion activated by glucagon, cortisol, adrenaline, growth hormone and thyroxine

19
Q

How are TAGs transported to adipose tissue?

A

In chylomicrons

20
Q

Describe how fatty acid synthesis differs from fatty acid degradation (beta oxidation)

A
21
Q

Which enzyme(s) are necessary for lipogenesis?

A

Fatty acid synthase complexes

22
Q

What role does acetyl co A carboxylase play in fatty acid synthesis?

A

Controls the rate of fatty acid synthesis. Can be regulated by: allosteric regulation, regulation by covalent modification of protein structure. Insulin activates by promoting dephosphorylation and glucagon/adrenaline inhibit the enzyme by promoting phosphorylation