Cell Respiration and Metabolism 113
space for every pair of electrons moved along the electron-
transport system. The second pump (the cytochrome c reduc-
tase complex) also transports 4 protons into the intermembrane
space, and the third pump (the cytochrome c oxidase complex)
transports 2 protons into the intermembrane space. As a result,
there is a higher concentration of H^1 in the intermembrane
space than in the matrix, favoring the diffusion of H^1 back out
into the matrix. The inner mitochondrial membrane, however,
does not permit diffusion of H^1 , except through the fourth
respiratory complex of proteins.
This last respiratory complex is a molecular machine, lik-
ened to a rotary turbine, that functions as an ATP synthase.
It contains a channel that permits the passage of H^1 from the
intermembrane space to the matrix, and it is this movement of
Coupling of Electron Transport
to ATP Production
According to the chemiosmotic theory, the electron-transport
system, powered by the transport of electrons, pumps protons
(H^1 ) from the mitochondrial matrix into the space between
the inner and outer mitochondrial membranes. The electron
transport system consists of four respiratory complexes com-
posed of about 90 proteins. Mitochondrial DNA codes for 13
of these proteins, and nuclear DNA codes for the rest. The
first three of these respiratory complexes serve as proton
pumps ( fig. 5.9 ).
The first pump (the NADH-coenzyme Q reductase com-
plex) transports 4 H^1 from the matrix to the intermembrane
Figure 5.7 The complete citric acid cycle. Notice that, for each “turn” of the cycle, 1 ATP, 3 NADH, and 1 FADH 2 are
produced.
FAD
FADH 2
AT P
NADH
NAD
NAD
NADH
GTP GDP
2H
2H
2H
+ H+
+ H+
Oxaloacetic acid (C 4 )
Acetyl CoA (C 2 )
Malic acid (C 4 )
Fumaric acid (C 4 )
Succinic acid (C 4 )
Citric acid (C 6 )
Isocitric acid (C 6 )
훂-Ketoglutaric acid (C 5 )
cis-Aconitic acid (C 6 )
NADH
NAD
2H
+ H+
1
2
3
4
5
6
7
8
HCCSCoA+ H 2 O
HS CoA
HO
H
H
H
H
HOOC H
H
C
C
OH
COOH
COOH
COOH
HH
C
C
O
COOH
COOH
C
C
H
HH
C
C
H
COOH
COOH
H
HO COOH
C
C
H
COOH
HCH
COOH
H
H COOH
C
C
H
COOH
HCOH
COOH
H
H H
C
C
H
COOH
CO
COOH
H
COOH
C
C
H
COOH
CH
COOH
H 2 O
H 2 O
H 2 O
H 2 O
CO 2
CO 2
H 2 O
ADP