Energy Production From Carbohydrates Flashcards

1
Q

What are the major functions of the pentose phosphate pathway?

A

Produce NADPH in cytoplasm, reducing power for anabolic processes, maintains free -SH in RBC on cysteine, produce C5 ribose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Write a reaction for phase I of pentose phosphate pathway

A

G6P + 2NADP —> C5 sugar phosphate + 2NADPH + 2H+ + 2CO2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Write a reaction for phase II of pentose phosphate pathway

A

3C5 sugar phosphate —> 2 fructose-6-phosphate + glyceraldehyde-3-phosphate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What happens in G6PDH deficiency?

A

Disulphide bridge formation in RBC due to low levels of NADPH. Insoluble aggregates called heinz bodies form - premature destruction of RBC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Draw out the glycolysis pathway

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Give the equations for the 3 committing steps in glycolysis

A

Glucose —> G6P

F6P —> F-1,6-P

PEP —> pyruvate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What does pyruvate dehydrogenase catalyse?

A

This reaction is irrversible

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What control mechanisms is PDH subject?

A

Acetyl CoA allosterically inhibits PDH, ADP promotes, ATP/NADH inhibit, activated when there is a lot of glucose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the functions of glycolysis?

A

Oxidises glucose, 2 NADH produced, net synthesis of 2 ATP, produces C6 and C3 intermediates (glycerol phosphate, 2,3-BPG)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What ismoers are carbohydrates usually found in the body?

A

D isomers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

List the main features of glycolysis

A

Oxidative, exergonic, C6–>2 C3, no loss of CO2, ATP generated, useful intermediates, substrate level phosphorylation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Write an equation for dihydroxyacetone phosphate going to glycerol phosphate

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What stimulates pyruvate kinase?

A

High insulin:glucagon ratio

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What inhibits phosphofructokinase?

A

High levels of ATP cause allosteric inhibition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Where would you find glucokinase and hexokinase?

A

Hexokinase - liver and muscle

Glucokinase - liver only

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What stimulates hexokinase and glucokinase?

A

An increase in glucose (or a decrease in G6P)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Why is lactate dehydrogenase needed?

A

RBC cannot regenerate NAD+ any other way

18
Q

Write the reaction that occurs in RBC to produce pyruvate

A
19
Q

Write the overall equation for glycolysis

A

Glucose + 2Pi + 2ADP + 2NAD+ —> 2 pyruvate + 2H2O + 2H+ + 2NADH + 2ATP

20
Q

Draw out the TCA cycle

A
21
Q

Where does the TCA cycle occur?

A

Mitochondiral matrix

22
Q

What does the TCA pathway require?

A

NAD+, FAD and oxaloacetate

23
Q

What is the main function of the TCA cycle?

A

Break the C-C bond in acetate and oxidise the atoms to CO2. Doesn’t function anaerobically

24
Q

Approximately how many molecules of ATP are produced per molecule of glucose in the TCA cycle?

A

36 molecules of ATP per molecule of glucose

25
Q

What are the catabolic functions of the TCA cycle?

A

Produces intermediates and interconvertible acids

26
Q

What are the anabolic functions of the TCA cycle?

A

Synthesis of non-essential amino acids, synthesis of haem and glucose, synthesis of fatty acids

27
Q

What are the two major signals for the TCA cycle?

A

ATP/ADP ratio and NADH/NAD+ ratio

28
Q

What is removed from acetate and which molecules accept them?

A

H+ and e- are removed by NAD+ and FAD

29
Q

Where does oxidative phosphorylation occur?

A

Inner mitochondrial membrane

30
Q

Briefly describe oxidative phosphorylation

A

e-‘s from NADH and FADH2 are transferred to O2, releasing energy. This can be used to drive ATP synthesis

31
Q

What is the role of proton translocating complexes?

A

Move protons from inside the inner mitochondrial matrix to outside the inner mitochondrial matrix, causing an increase in H+ and therefore creating proton motive force. 3 out of 4 complexes are PTC

32
Q

Describe the effect of the proton motive force

A

As the inner mitochondrial membrane is impermeable to protons there is a build up of H+. Protons can only re-enter the mitochondrial matrix via ATPsynthase complexes.

33
Q

How many moles of ATP can 2 moles of NADH produce?

A

5 moles of ATP

34
Q

How many moles of ATP can 2 moles of FADH2 produce?

A

3 moles of ATP

35
Q

Describe what happens in the mitochondria when ATP is high

A

ATPsynthase stops (lack of substrate), prevents H+ moving back into the mitochondria, H+ conc out increases such that protons cannot be pumped out, electron transport stops

36
Q

What is the function of uncoupling proteins?

A

Uncouple electron transport from ATP production to produce heat (leaky membranes)

37
Q

What does UCP1 do?

A

Expressed in brown adipose and is involved in non-shivering thermogenesis

38
Q

What does UCP2 do?

A

Linked to obesity, metabolic syndrome and heart faiulre

39
Q

What does UCP3 do?

A

Found in skeletal muscle, brown adipose and heart. Involved in modifying fatty acid metabolism and in protecting against ROS damage

40
Q

What does noradrenaline stimulate?

A

Lipolysis - fatty acids - NADH/FAD2H - increase in pmf

Also activates UCP1

41
Q

Describe the differences between substrate level phosphorylation and oxidative phosphorylation

A
42
Q
A