Metabolism 4 - The Krebs Cycle Flashcards

1
Q

What is acetyl coA?

A

A molecule which contains a high energy thioester bond, which is hydrolysed to donate acetate to other molecules.

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2
Q

How does the krebs cycle start?

A

Oxaloacetate is converted to citrate by the addition of acetyl-coA.
Enzyme - Citrate synthase
Makes HS-coA

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3
Q

What is the second reaction of the krebs cycle?

A

Citrate is converted to isocitrate by aconitase. (Isomerisation)

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4
Q

What is the third reaction of the krebs cycle?

A

Isocitrate is converted to a-ketoglutarate by isocitrate dehydrogenase (using NAD+ and releasing CO2)

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5
Q

What is the fourth reaction of the krebs cycle?

A

a-ketoglutarate is converted to succinyl coA. Uses NAD+, HS-CoA and catalysed by the a-ketoglutarate dehydrogenase complex.

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6
Q

What is the fifth reaction of the krebs cycle?

A

Succinyl-CoA is converted to succinate using succinate CoA synthetase. This reaction makes GTP.

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7
Q

What is reaction 6 of the Krebs cycle?

A

Succinate is converted to fumarate using succinate dehydrogenase. This enzyme is located at the inner mitochondrial membrane, and FAD is reduced.

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8
Q

What is the seventh stage of the krebs cycle?

A

Fumarate is converted to malate, with the addition of H2O. This is catalysed by fumarase

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9
Q

What is the final stage of the krebs cycle?

A

The dehydrogenation of malate, catalysed by malate dehydrogenase, to reform oxaloacetate.

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10
Q

What are the net products of the krebs cycle?

A

There are two molecules of CO2 produced, three molecules of NADH, one molecule of FADH2, and one molecule of GTP.

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11
Q

What is the location of the enzymes in the krebs cycle enzymes?

A

All the enzymes, bar succinate dehydrogenase, are foudn in the mitchondrial matrix. Succinate dehydrogenase is in the inner mitochondrial membrane, it communicates directly with components in the electron transport chain.

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12
Q

How does degradation of amino acids occur?

A

The amino group is removed and excreted as urea. This is done by a transamination reaction. The carbon skeleton is funnelled into glucose production or enters the Kress cycle.

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13
Q

Define a transamination reaction

A

A reaction where an amino group is transferred from one amino acid to a keto acid, forming a new pair of amino and keto acids

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14
Q

Describe the transamination of alanine

A

Alanine reacts with a-ketaglitarate by alanine aminotransferase. This makes pyruvate and glutamate.

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15
Q

What are the two pumps involved in NADH transportation?

A

The glycerol phosphate shuttle and the malate aspartate shuttle.

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16
Q

Where is the glycerol phosphate shuttle used?

A

Skeletal muscle and brain

17
Q

Where in the body is the malate-aspartate shuttle used?

A

The liver, kidney and heart.

18
Q

Describe the process that occurs in the glycerol phosphate shuttle

A
  • Glycerol 3-phosphate dehydrogenase transfers electrons from NADH to dihydroxyacetone phosphate to generate glycerol 3-phosphate (cytosol)
  • A membrane bound form of the same enzyme transfers electrons to FAD
  • Electrons are passed on to coenzyme Q
19
Q

Describe the reactions that occur in the Malate-Aspartate shuttle.

A
  • The main reactions are oxaloacetate taking an electron from NAD to make malate, which is then transported across the membrane and oxidised to make NADH.
  • So this can continue, transamination reactions occur. Oxaloacetate and glutamate react to form a-ketoglutarate and aspartate, and vice versa
20
Q

Why do transamination reactions occur in the malate-aspartame shuttle?

A
  • Malate travels into the mitochondria through an alpha-keyoglutarate transporter.
  • A glutamate aspartate transporter is also needed so the oxaloacetate can react with glutamate
21
Q

How are catabolic and anabolic pathways kept separate?

A

NADPH is used in anabolic reactions, and NADH is used in catabolic reactions. This keeps electron transport separate.

22
Q

How are NADP+ and NAD+ different?

A

They are different by one phosphate group.

23
Q

Give examples of pathways where NADP is used.

A

Thymidine synthesis and the synthesis of cholesterol.