Energy Production - TCA cycle Flashcards

1
Q

WHere does the TCA cycle take place?

A

Mitochondria

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

What is the main substances needed by the pathway?

A

The pathway requires NAD+, FAD and oxaloacetate.

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

What is the main function of the TCA cycle?

A

The main function of the pathway is to break the C-C bond in acetate (as acetyl~CoA) and oxidise the C-atoms to CO2.

The H+ and e- removed from acetate are transferred to NAD+ and FAD.

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

Can this reaction take place in the absence of oxygen?

A

No

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

Why are there no known genetic defects in the pathway?

A

It would be lethel

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

What is the role of pyruvate dehydrogenase (PDH) in the TCA cycles?

A

Pyruvate transported from cytoplasm across mitochondrial
membrane

PDH is a large multi-enzyme complex (5 enzymes) that converts pyruvate Acetyl coA which is used in the TCA cycle

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

What activates and inhibits PDH?

A
activated by: 
Pyruvate 
CoASH 
NAD+ 
ADP 
Insulin dephosphorylation
inhibited by:
acetyl-CoA
NADH
ATP
citrate
phosphorylation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How does PDH work?

A

It converts pyruvate to acetyl coA via irreversible loss of Co2

The different enzyme activities require various cofactors (FAD,
thiamine pyrophosphate and lipoic acid).

B-vitamins provide
these factors, so reaction is sensitive to Vitamin B1 deficiency.

Reaction is irreversible, so is a key regulatory step and pyruvate therefore cannot be formed from Acetyl CoA

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

What disease does PDH deficiency lead to?

A

Lactic acidosis

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

How is the TCA cycle regulated?

A

It’s oxidative - requires oxygen

It’s s ingle pathway

It is activated and inhibited by various molecules

Pyruvate is converted to Acetyl coA in an irreversible reaction

It is regulated by energy availability - increase in NADH succinyl-CoA and ATP leads to inhibition and increase in ADP leads to activation

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

How many cycles of the TCA cycle are there?

A

2 cycles for every glucose entering glycolysis

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

Which enzymes in the cycle regulate the TCA cycle?

A

a-ketoglutarate dehydrogenase
- - NADH, ATP,
succinyl-CoA

Isocitrate dehydrogenase
- One of the early irreversible steps of the TCA cycle (catalysed by isocitrate dehydrogenase) is allosterically inhibited by the high-energy signal NADH and activated by the low-energy signal ADP.

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

Which precursors for biosynthesis

does the TCA cycle produce?

A

Fatty acids
Amino acids
Haem synthesis
Glucose

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

Describe the roles of the tricarboxylic acid cycle (TCA cycle) in
metabolism.

A

• Mitochondrial

• Central pathway in the catabolism of sugars, fatty acids, ketone
bodies, amino acids, alcohol

  • Strategy - to produce molecules that readily lose CO2
  • Breaks C-C bond in acetate (acetyl~CoA); carbons oxidised to CO
  • Oxidative producing NADH and FADH
  • Some energy as GTP (  ATP) produced directly
  • Produces precursors for biosynthesis
  • Does not function in absence of O

• Intermediates act catalytically - no net synthesis or degradation of
Krebs cycle intermediates alone

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

List the end-products of glycolysis under aerobic and anaerobic conditions in red blood cells and skeletal muscle.

A

-

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

Outline the important roles of pyruvate dehydrogenase in glucose metabolism.

A

-

17
Q

List the functions of the TCA cycle

A

-

18
Q

Explain the consequences of a genetic defect that prevented the synthesis of one of the enzymes of the TCA cycle (N.B. this refers to a complete enzyme deletion).

A

-

19
Q

Describe the key features of electron transport and explain how the proton motive force (p.m.f) is produced.

A

-

20
Q

Describe the relationship between electron transport and ATP synthesis.

Explain how this relationship is altered during thermogenesis in brown
adipose tissue mitochondria.

A

-

21
Q

Compare and contrast the processes of oxidative phosphorylation and substrate level phosphorylation.

A

-

22
Q

Explain why cyanide is toxic to cells.

A

-

23
Q

List the three ketone bodies produced in humans and explain why they are only produced under certain conditions.

A

-