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Cambridge International A Level Biology Revision Guide

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Chapter 12: Energy and respiration<br />

great deal of chemical potential energy. When free oxygen<br />

is available, some of this energy can be released via the<br />

Krebs cycle and oxidative phosphorylation. However, the<br />

pyruvate first enters the link reaction, which takes place in<br />

the mitochondria (page 275).<br />

The link reaction<br />

Pyruvate passes by active transport from the<br />

cytoplasm, through the outer and inner membranes of<br />

a mitochondrion and into the mitochondrial matrix.<br />

Here it is decarboxylated (this means that carbon dioxide<br />

is removed), dehydrogenated (hydrogen is removed)<br />

and combined with coenzyme A (CoA) to give acetyl<br />

coenzyme A. This is known as the link reaction<br />

(Figure 12.9). Coenzyme A is a complex molecule<br />

composed of a nucleoside (adenine plus ribose) with a<br />

vitamin (pantothenic acid), and acts as a carrier of acetyl<br />

groups to the Krebs cycle. The hydrogen removed from<br />

pyruvate is transferred to NAD.<br />

pyruvate + CoA + NAD<br />

acetyl CoA + CO 2<br />

+ reduced NAD<br />

Fatty acids from fat metabolism may also be used to<br />

produce acetyl coenzyme A. Fatty acids are broken down<br />

in the mitochondrion in a cycle of reactions in which<br />

each turn of the cycle shortens the fatty acid chain by<br />

a two-carbon acetyl unit. Each of these can react with<br />

coenzyme A to produce acetyl coenzyme A, which, like<br />

that produced from pyruvate, now enters the Krebs cycle.<br />

The Krebs cycle<br />

The Krebs cycle (also known as the citric acid cycle or<br />

tricarboxylic acid cycle) was discovered in 1937 by Hans<br />

Krebs. It is shown in Figure 12.9.<br />

The Krebs cycle is a closed pathway of enzymecontrolled<br />

reactions.<br />

■■<br />

■■<br />

■■<br />

Acetyl coenzyme A combines with a four-carbon<br />

compound (oxaloacetate) to form a six-carbon<br />

compound (citrate).<br />

The citrate is decarboxylated and dehydrogenated in a<br />

series of steps, to yield carbon dioxide, which is given<br />

off as a waste gas, and hydrogens which are accepted by<br />

the carriers NAD and FAD (page 275).<br />

Oxaloacetate is regenerated to combine with another<br />

acetyl coenzyme A.<br />

For each turn of the cycle, two carbon dioxide molecules<br />

are produced, one FAD and three NAD molecules are<br />

reduced, and one ATP molecule is generated via an<br />

intermediate compound.<br />

Although part of aerobic respiration, the reactions<br />

link<br />

reaction<br />

oxaloacetate (4C)<br />

(4C)<br />

(4C)<br />

reduced<br />

FAD<br />

ATP<br />

ADP<br />

reduced<br />

NAD<br />

NAD<br />

(4C)<br />

pyruvate (3C)<br />

NAD<br />

CO 2<br />

reduced<br />

NAD<br />

acetyl (2C) CoA<br />

FAD<br />

Krebs cycle<br />

(4C)<br />

reduced<br />

NAD<br />

NAD<br />

reduced<br />

NAD<br />

NAD<br />

Figure 12.9 The link reaction and the Krebs cycle.<br />

CoA<br />

of the Krebs cycle make no use of molecular oxygen.<br />

However, oxygen is necessary for the final stage of aerobic<br />

respiration, which is called oxidative phosphorylation.<br />

The most important contribution of the Krebs cycle to<br />

the cell’s energetics is the release of hydrogens, which can<br />

be used in oxidative phosphorylation to provide energy to<br />

make ATP.<br />

QUESTION<br />

citrate (6C)<br />

(6C)<br />

(5C)<br />

12.2 Explain how the events of the Krebs cycle can be<br />

cyclical.<br />

CO 2<br />

CO 2<br />

Oxidative phosphorylation and the<br />

electron transport chain<br />

In the final stage of aerobic respiration, oxidative<br />

phosphorylation, the energy for the phosphorylation<br />

of ADP to ATP comes from the activity of the electron<br />

transport chain. Oxidative phosphorylation takes place in<br />

the inner mitochondrial membrane (Figure 12.10).<br />

273

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