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Cambridge International A Level Biology Revision Guide

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<strong>Cambridge</strong> <strong>International</strong> A <strong>Level</strong> <strong>Biology</strong><br />

270<br />

ATP<br />

ATP as energy ‘currency’<br />

Look back at the structure of ATP, shown in Figure 6.4,<br />

page 113.<br />

When a phosphate group is removed from ATP,<br />

adenosine diphosphate (ADP) is formed and 30.5 kJmol −1 of<br />

energy is released. Removal of a second phosphate produces<br />

adenosine monophosphate (AMP), and 30.5 kJ mol −1 of<br />

energy is again released. Removal of the last phosphate,<br />

leaving adenosine, releases only 14.2 kJ mol −1 (Figure 12.4).<br />

In the past, the bonds attaching the two outer phosphate<br />

groups have been called high-energy bonds, because<br />

more energy is released when they are broken than<br />

when the last phosphate is removed. This description is<br />

misleading and should be avoided, since the energy does<br />

not come simply from breaking those bonds, but rather<br />

from changes in chemical potential energy of all parts of<br />

the system.<br />

ATP + H 2 O<br />

ADP + H 2 O AMP + H 2 O adenosine<br />

30.5 kJ mol –1 30.5 kJ mol –1 14.2 kJ mol –1<br />

P i P i P i<br />

Figure 12.4 Hydrolysis of ATP (P i<br />

is inorganic phosphate,<br />

H 3<br />

PO 4<br />

).<br />

These reactions are all reversible. It is the<br />

interconversion of ATP and ADP that is all-important in<br />

providing energy for the cell:<br />

ATP + H 2<br />

O ADP + H 3<br />

PO 4<br />

± 30.5 kJ<br />

The rate of interconversion, or turnover, is enormous. It is<br />

estimated that a resting human uses about 40 kg of ATP<br />

in 24 hours, but at any one time contains only about 5 g of<br />

ATP. During strenuous exercise, ATP breakdown may be<br />

as much as 0.5 kg per minute.<br />

The cell’s energy-yielding reactions are linked to<br />

ATP synthesis. The ATP is then used by the cell in<br />

all forms of work. ATP is the universal intermediary<br />

molecule between energy-yielding and energy-requiring<br />

reactions used in a cell, whatever the type of cell. In other<br />

words, ATP is the ‘energy currency’ of the cell. The cell<br />

‘trades’ in ATP, rather than making use of a number of<br />

different intermediates. ATP is a highly suitable molecule<br />

for this role. Not only is it readily hydrolysed to release<br />

energy, it is also small and water-soluble. This allows it to<br />

be easily transported around the cell.<br />

Energy transfers are inefficient. Some energy is<br />

converted to thermal energy whenever energy is<br />

transferred. At the different stages in a multi-step<br />

reaction such as respiration, the energy made available<br />

may not perfectly correspond with the energy needed<br />

to synthesise ATP. Any excess energy is converted to<br />

thermal energy. Also, many energy-requiring reactions<br />

in cells use less energy than that released by hydrolysis of<br />

ATP to ADP. Again, any extra energy will be released as<br />

thermal energy.<br />

Be careful to distinguish between molecules used<br />

as energy currency and as energy storage. An energy<br />

currency molecule acts as the immediate donor of energy<br />

to the cell’s energy-requiring reactions. An energy<br />

storage molecule is a short-term (glucose or sucrose)<br />

or long-term (glycogen, starch or triglyceride) store of<br />

chemical potential energy.<br />

Synthesis of ATP<br />

Energy for ATP synthesis can become available in two<br />

ways. In respiration, energy released by reorganising<br />

chemical bonds (chemical potential energy) during<br />

glycolysis and the Krebs cycle (pages 272–273) is used to<br />

make some ATP. However, most ATP in cells is generated<br />

using electrical potential energy. This energy is from the<br />

transfer of electrons by electron carriers in mitochondria<br />

and chloroplasts. It is stored as a difference in proton<br />

(hydrogen ion) concentration across some phospholipid<br />

membranes in mitochondria and chloroplasts, which<br />

are essentially impermeable to protons. Protons are then<br />

allowed to flow down their concentration gradient (by<br />

facilitated diffusion) through a protein that spans the<br />

phospholipid bilayer. Part of this protein acts as an enzyme<br />

that synthesises ATP and is called ATP synthase. The<br />

transfer of three protons allows the production of one ATP<br />

molecule, provided that ADP and an inorganic phosphate<br />

group (P i<br />

) are available inside the organelle. This process<br />

occurs in both mitochondria (page 275) and chloroplasts<br />

(page 288) and is summarised in Figure 12.5. The process<br />

was first proposed by Peter Mitchell in 1961 and is called<br />

chemiosmosis.<br />

Note that a hydrogen atom consists of one proton and<br />

one electron. The loss of an electron forms a hydrogen<br />

ion, which is a single proton.<br />

H<br />

H + + e −

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