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Chemiosmotic Theory June 2013
Chemiosmotic Theory June 2013
The mitochondria of animal cells can use energy made available in metabolic reactions,
such as those involved in the oxidation of sugars and fats, to make ATP. The process is
known as "oxidative phosphorylation"; energy released by oxidation is used to drive the
phosphorylation of ADP to ATP.
The location of the proteins and cofactors used in oxidative phosphorylation is important
in the process (see Figure 1).
NAD+ is reduced to NADH in the matrix of mitochondria by enzymes of the Krebs cycle.
The respiratory chain proteins and the ATP synthase enzyme are located in the inner
mitochondrial membrane.
The chemiosmotic theory was developed by the British biochemist, Peter Mitchell, to
explain the mechanism of oxidative phosphorylation in mitochondria (and
photophosphorylation in chloroplasts). He was awarded the Nobel Prize in 1978. The
processes of oxidative phosphorylation are summarised in Figure 2.
NADH produced in the Krebs cycle passes electrons to the respiratory chain and becomes
re-oxidized to NAD+. The electrons are transported down the chain to oxygen releasing
energy (think of burning sugar or fat); the reduction of oxygen forms water. Thus,
oxygen is the terminal electron acceptor of the mitochondrial respiratory chain. The
respiratory chain is shown by the red box in Figure 2.
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Electron transport through the complexes of the respiratory chain causes uptake of H +
from the matrix at the inside surface of the inner membrane, and the release of H + at the
outside surface (Figures 2 and 4). Protons are effectively moved (or "pumped") outwards
across the inner membrane using energy released in the electron transport reactions. The
movement of H+ makes the outer aqueous region positive and slightly acidic relative to
the matrix of the mitochondrion. This difference between the two sides of the membrane
(it is both an electrical and a pH difference) is called the protonmotive force, and it can
drive protons back across the membrane through the ATP synthase enzyme. Proton flow
through the enzyme causes a rotation of protein subunits in the ATP synthase which leads
to ATP synthesis from ADP and phosphate. Another British biochemist, John Walker, and
Paul Boyer from the US, shared the Nobel Prize for Chemistry in 1997 for their work on
this reaction.
A key point to understand is that the protonmotive force is an intermediate in the transfer
of energy from the oxidation/reduction reactions of the respiratory chain to ATP
synthesis.
It is important to note that the generation of the protonmotive force and ATP synthesis
occur even when the outer mitochondrial membrane is removed in experiments; the outer
membrane does not have a role in oxidative phosphorylation.
Bacteria do not have mitochondria. Many species of bacteria (including Escherichia coli)
have respiratory chains and ATP synthases in their cytoplasmic membrane (which lies
just inside their outer membrane/cell wall). Like mitochondria these bacteria perform
oxidative phosphorylation with a protonmotive force as the energy intermediate.
This document was kindly provided by Martin D Brand (Buck Institute, California),
Stuart J Ferguson (University of Oxford), J Baz Jackson (University of Birmingham),
David G Nicholls (Buck Institute, California), Peter R Rich (University College,
London).
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