Energy II Flashcards

1
Q

Citric acid cycle

A
  1. Glucose is broken down into 2 pyruvate molecules
  2. In the presence of oxygen, each pyruvate is made into acetyl CoA
  3. Pyruvate reacts with oxaloacetate to form citrate
  4. Isomerases into isocitrate
  5. Made into alpha-ketogluterate after decarboxylation and NADH production
  6. Made into succinyl CoA after decarboxylation and NADH production
  7. Oxaloacetate molecule made after GTP production, FADH2 production and NADH production
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the net gain of the citric acid cycle

A
  • 6 NADH
  • 2 GTP
  • 2 FADH2
  • 2 CO2
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What regulates entry into the citric acid cycle and why

A

Pyruvate dehydrogenase since it turns pyruvate into acetyl CoA which commits the glucose carbon skeleton to either oxidation to CO2 and energy production or fatty acid synthesis

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

How is pyruvate dehydrogenase regualted

A

Inhibited by its product NADH and acetyl CoA through feedback inhibition and also its inhibited by phosphorylation

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

How is pyruvate dehydrogenase regulated in muscle

A

Its activated via the action of a phosphatase, which itself is stimulated by Ca2+

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

How is calcium regulated in liver

A

Adrenaline causes an increase in calcium concentration through the activation of alpha adrenergic receptors and IP3

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

What happens in the liver and adipose tissue when glucose concentrations are high

A

Insulin is secreted which stimulates phosphatase which funnels glucose to fatty acid synthesis

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

What regulates citrate synthase action

A

Citrate

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

What regulates isocitrate dehydrogenase

A

NADH and ATP

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

What stimulates isocitrate dehydrogenase

A

ADP

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

What regulates alpha-keto gluterate dehydrogenase

A

NADH, ATP and succinyl CoA

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

What is beriberi

A

Its a deficiency in thiamine (Vit B1)

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

Where is beriberi common and what are the symptoms

A

In the far east where rice is staple

characterised by cardiac and neurological symptoms

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

Why does beriberi occur

A

Thiamine is a prosthetic group for pyruvate and alpha-keto-gluterate
Therefore when thiamine is deficient these enzymes are compromised and cannot function properly, so the generation of ATP is reduced

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

How does oxidative phosphorylation work

A
  1. The NADH/FADH2iiii will donate a H atom, which will split into a proton and an electron
  2. The electron will be passed from complex 1 all the way to complex IV down the electron transport chain
  3. As it does this, the electron will loose energy, this will be used to pump protons into the inter-membrane space
  4. An electrochemical gradient is set up, called the proton motive force
  5. ATP is generated when protons move down their concentration gradient to add Pi to ADP to create ATP
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How much ATP is generated from NADH and FADH2 and why

A

every NADH forms 3 ATP
every FADH2 forms 2 ATP
FADH2 only enters the electron transport chain at complex II therefore more energy is released from NADH2

17
Q

Why do newborn babies have brown fat

A

Brown fat is rich in mitochondria that have uncoupling proteins
this protein allows protons to move back into the mitochondrial matrix instead of ATP synthase
The energy released is not used to make ATP but rather is released as heat

18
Q

what is an OXPHOS disease

A

A common degenerative disease thats caused by mutations in genes encoding proteins of electron transport chain
Symptoms; fatigue, epilepsy and dementia

19
Q

What regulates the electron transport chain

A

Its governed by the need for ATP, regulated uncoupling leads to the generation of heat