Energy Production-carbs 4 Flashcards

1
Q

What is the role of pyruvate dehydrogenase in glucose metabolism?

A

It converts Pyruvate (3C molecule) into acetylCoA (2C molecule) to the enter the tricarboxylic acid/Krebs cycle.

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2
Q

What is released when Pyruvate becomes AcetylCoA? What does this mean for the reaction?

A

A CO2 is released, therefore an irreversible reaction.

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3
Q

Describe some factors of the Krebs cycle.

A
A single pathway
Catabolism of sugars, fatty acid, ketone bodies,amino acids and alcohol 
Produces molecules that readily lose CO2
Oxidises carbons from acetate to CO2
Oxidative producing NADH and FADH2
Some energy produced as GTP
Produce precursors for biosynth 
Not function in O2 absence 
Intermediates act catalytically
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4
Q

What happens in the Krebbs cycle? (Overview not specific details)?

A

ACetylCoA joins a C4 molecule to form citrate (C6)
CO2 is released twice for every acetylCoA
Reaction of NAD and FAD occur
Phosphorylation of GDP to GTP X2
CoA is released
6 NADH released
2 FADH2 releases

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5
Q

What is the Krebbs/TCA cycle regulated by?

A

Regulated by energy availability like glycolysi
The product succinylcholine-CoA inhibits it
Inhibited by high levels ATP/acetyl-CoA/NADH/citrate
Activated by high levels of pyruvate/insulin/CoASH/ADP

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6
Q

Where does the TCA/Krebbs cycle occur?

A

In the mitochondrial matrix

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7
Q

Where do electrons travel in the electron transport chain?

A

From the mitochondrial matrix through the inner mitochondrial membrane, losing energy as they ass down the electron carriers.

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8
Q

What happens to the energy released by the e- transport chain?

A

30% of it is used to transport H+ molecules across the membrane into the inter membrane space to create a gradient.
The rest is lost as heat to keep the body warm

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9
Q

Where do the e- and H+ come from in the electron transport chain?

A

NADH + H+(2H+ =2e-) turns to NAD+

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10
Q

Where do the electrons format he transport chain go?

A

They join 2H+ and one O to form H2O.

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11
Q

What is the proton motive force?

A

The energy that e- provides to push H+ across the inner mitochondrial membrane and make a gradient.

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12
Q

Why do proteins return to the matrix?

A

It’s favoured energetically by the electrochemical gradient (electrical and chemical gradient)

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13
Q

How do H+ cross the mitochondral membrane?

A

They are forced through ATP Synthase becase the membrane is highly impermeable. This drives ATP synthesis.

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14
Q

How is oxidative phosphorylation regulated?

A

When ATP is high, there is low ADP so no substrate for ATP synthesis.
Inward flow of H+ into matrix stops
Conc of H+ in intermembrane space is high
Prevents further H+ pumping, as electron energy not enough to overcome high conc gradient.
Less NADH is used up this circles back and stops other glycolysis pathways.

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15
Q

How do inhibitors stop oxidative phosphorylation?

A

Cyanide inhibitors block the electron transport.
Stops acceptance of electrons by O2.
Transport chain stops as electrons back up
H+ pumping stops

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16
Q

How do uncouplers inhibit oxidative phosphorylation?

A

They increase permability of mitochondrial inne rmembrane to protons.
This stops the H+ conc building up so H+ isn’t forced through ATP Synthase by the proton motive force
No ATP is made

17
Q

How do Oxy/Phos diseases inhibit oxidative phosphorylation?

A

Genetic defects in proteins encoded by mtDNA

Decrease electron transport and or ATP synthesis

18
Q

How does coupling effect the efficiency of oxidative phosphorylation and hw does the body exploit this?

A

Tighter coupling increases efficiency (less heat loss)

In brown adipose tissue, the degree of coupling is controlled by fatty acids (uncouplers) this allows extra heat generation.

Brown adipose tissue is found surrounding newborns organs and in hibernating mammals

19
Q

How does brown adipose tissue change the degree of coupling?

A

Noradrenaline responds t cold activating lipase

Lipase release fatty acids from triaglycerol

These are oxidised to NADH/FADH2 causing e- transport

Fatty acids activate UCP1

UCP1 transports H+ back to mitochondria instead of ATP synth

Energy of proton motive force us used for heat instead increasing body temp