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Cambridge International A Level Biology Revision Guide

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Chapter 12: Energy and respiration<br />

CO 2 glucose O 2<br />

cell surface membrane of cell<br />

mitochondrion<br />

glycolysis<br />

pyruvate<br />

cytoplasm<br />

mitochondrial envelope<br />

intermembrane space<br />

link reaction<br />

inner<br />

membrane<br />

outer<br />

membrane<br />

ATP<br />

ACoA<br />

Krebs<br />

cycle<br />

reduced<br />

NAD<br />

reduced<br />

FAD<br />

matrix<br />

H +<br />

electron<br />

transport<br />

chain<br />

ADP + P i<br />

ATP<br />

oxidative<br />

phosphorylation<br />

crista<br />

H +<br />

H 2 O<br />

Figure 12.11 The sites of the events of respiration in a cell. ACoA = acetyl coenzyme A.<br />

molecule entering the chain produces on average two and a<br />

half molecules of ATP, and each reduced FAD produces one<br />

and a half molecules of ATP. The number of ATP molecules<br />

actually produced varies in different tissues and different<br />

circumstances, largely dependent on how much energy is used<br />

to move substances into and out of the mitochondria.<br />

Hydrogen carrier molecules<br />

NAD is made of two linked nucleotides (Figure 12.12).<br />

Both nucleotides contain ribose. One nucleotide<br />

contains the nitrogenous base adenine. The other has a<br />

nicotinamide ring, which can accept a hydrogen ion and<br />

two electrons, thereby becoming reduced.<br />

NAD + 2H reduced NAD<br />

NAD + + 2H NADH + + H +<br />

A slightly different form of NAD has a phosphate group<br />

instead of the hydrogen on carbon 1 in one of the ribose<br />

rings. This molecule is called NADP (nicotinamide<br />

adenine dinucleotide phosphate) and is used as a hydrogen<br />

carrier molecule in photosynthesis.<br />

FAD (flavin adenine dinucleotide) is similar in<br />

function to NAD and is used in respiration in the Krebs<br />

cycle. FAD is made of one nucleotide containing ribose<br />

and adenine and one with an unusual structure involving<br />

a linear molecule, ribitol, instead of ribose.<br />

O –<br />

nicotinamide ring<br />

O<br />

P<br />

O<br />

O<br />

CH 2<br />

H<br />

NH 2<br />

N<br />

N<br />

H<br />

N N<br />

O – P O CH 2<br />

O<br />

O<br />

H H<br />

H<br />

H<br />

OH<br />

OH OH<br />

Key<br />

replaced by a phosphate group in NADP<br />

site which accepts electrons<br />

Figure 12.12 NAD (nicotinamide adenine dinucleotide). You<br />

do not need to learn the structure of this molecule, but may<br />

like to compare it with the units that make up DNA and RNA.<br />

O<br />

H<br />

OH<br />

N<br />

H<br />

H<br />

H<br />

O<br />

C<br />

NH 2<br />

ribose<br />

adenine<br />

ribose<br />

275

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