Acetyl CoA, Mitochondria & O2 Flashcards

1
Q

When does aerobic respiration occur?

A

Only in the presence of O2

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2
Q

Where does Aerobic respiration occur?

A

In the mitochondria

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3
Q

Which processes are required to occur for aerobic respiration to occur?

A

Citric Acid Cycle

Oxidative Phosphorylation

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4
Q

What is the significance of aerobic respiration?

A

Yields more energy in ATP form

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5
Q

List the functions of mitochondria in a cell

A
  • Hydrolyse fatty acids into Acetyl CoA (gain energy)
  • Decarboxylate Pyruvate into Acetyl CoA
  • Citric Acid Cycle
  • Oxidative Phosphorylation
  • Thermogenesis
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6
Q

What is the significance of the Citric Acid Cycle?

A

Pivotal metabolic pathway generating reducing equivelants for ATP generation and metabolic intermediates for anabolic pathways

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7
Q

What is Thermogenesis?

A

When the energy stored in ATP is released to generate heat

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8
Q

Summarise Oxidative Phosphorylation

A

Formation of ATP from ADP + Pi
- reducing equivelants derived from the breakdown of
Acetyl CoA
- electrons combine with O2 to form H2O

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9
Q

Who is thermogenesis especially useful for?

A

Infants and mammals living in low temp

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10
Q

What gives brown fat cells their brown colour?

A

They contain lots of mitochondria to generate heat giving them brown appearance

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11
Q

What are the products of the Citric Acid Cycle?

A

3NADH, 2FADH, 1 GTP

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12
Q

Outline the stages of the citric acid cycle

A

In presence of O2
- Pyruvate converted to Acetyl CoA (2C)
- Acetyl CoA reacts with oxaloacetate acid (4C)
=> forms citrate (6C)
- Citrate loses 2CO2 molecules via a series of reactions
- 3 NADH and 2FADH molecules are released
- 1 GTP molecule is formed

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13
Q

Where do the electrons required for oxidative phosphorylation come from?

A

The Citric Acid Cycle

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14
Q

How is the Citric Acid Cycle regulated?

A

The formation of Acetyl CoA from pyruvate is irreversible

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15
Q

Why is the Citric Acid Cycle so significant to the whole body?

A

Integrates Carbohydrate, lipid and protein metabolism
- source of building blocks for most important bio
molecules

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16
Q

How does formation of Acetyl CoA from Pyruvate being irreversible regulate the cycle?

A

This commits the glucose carbon skeleton to either oxidation or fatty acid synthesis

17
Q

What enzyme is involved in the conversion of pyruvate into Acetyl CoA?

A

Pyruvate Dehydrogenase

18
Q

How is the conversion of pyruvate to Acetyl CoA inhibited?

A

Inhibited by NADH and Acetyl CoA

Regulated by phosphatase and kinase

19
Q

How does the reaction occur in muscle?

A

Pyruvate dehydrogenase activated by a phosphatase stimulated by calcium ions

20
Q

How is the phosphatase enzyme stimulated in the liver?

A

Insulin stimulates phosphatase which funnels glucose to fatty acid synthesis

21
Q

How is fatty acid synthesis triggered?

A

Adrenaline increases calcium influx through the activation of adrenergic receptors and IP3

22
Q

How does NADH and Acetyl CoA regulate glucose production?

A

Build up of NADH and Acetyl CoA inform sthe enzyme, the cells energy requirements are being met/ fatty acids are being hydrolysed
- spares glucose

23
Q

What is the BeriBeri disease?

A

Thiamine deficiency in thiamine (vitamin B1)
- thiamine is a prosthetic group for pyruvate and ɒ
ketogluterate dehydrogenase

24
Q

List some symptoms of Beriberi disease

A

Cardiac issues

neurological issues - common as glucose primary source of energy

25
What is the role of the electron transport chain?
ATP synthesis | involves removal of H+ from oxidisable substrates
26
How many protons are required to form one ATP molecule?
4H+ (3 protons = 1 ATP, 1H+ used to transport it out)
27
Outline the steps of the electron transport chain
1. H enter the transport chain 2. split into H+ and e- 3. e- passes through cytochrome enzymes 4. e- react with o2 forming H2O 5. H pumped across intermembranal matrix - down pH gradient creates transmembranal potential 6. H+ diffuses back into cytosol through ATP synthase 7. ATP synthase undergoes conformational change 8. Can now catalyse ATP production from ADP and Pi
28
How are degenerative disease caused?
Caused by mutations in e- transport protein genes
29
Name some degenerative diseases?
- fatigue - epilepsy - dementia
30
How is the electron transport chain regulated?
By the need of ATP | - tightly coupled to oxidative phosphorylation