The Mechanism of ATP Synthesis Is Shared Among Bacteria, Mitochondria, and Chloroplasts

Although bacteria lack internal membranes, aerobic bacteria nonetheless carry out oxidative phosphorylation by the same processes that occur in eukaryotic mitochondria and chloroplasts (Figure 12-30). Enzymes that catalyze the reactions of both the glycolytic pathway and the citric acid cycle are present in the cytosol of bacteria; enzymes that oxidize NADH to NAD+ and transfer the electrons to the ultimate acceptor O2 reside in the bacterial plasma membrane. The movement of electrons through these membrane carriers is coupled to the pumping of protons out of the cell. The movement of protons back into the cell, down their concentration gradient through ATP synthase, drives the synthesis of ATP. The bacterial ATP synthase (F0F1 complex) is essentially identical in structure and function to the mitochondrial and chloroplast ATP synthases, but is simpler to purify and study.

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FIGURE 12-30 ATP synthesis by chemiosmosis is similar in bacteria, mitochondria, and chloroplasts. In chemiosmosis, a proton-motive force generated by proton pumping across a membrane is used to power ATP synthesis. The mechanism and membrane orientation of the process are similar in bacteria, mitochondria, and chloroplasts. In each illustration, the membrane surface facing a shaded area is a cytosolic face; the surface facing an unshaded, white area is an exoplasmic face. Note that the cytosolic face of the bacterial plasma membrane, the matrix face of the inner mitochondrial membrane, and the stromal face of the thylakoid membrane are all equivalent. During electron transport, protons are always pumped from the cytosolic face to the exoplasmic face, creating a proton concentration gradient (exoplasmic face > cytosolic face) and an electric potential (negative cytosolic face and positive exoplasmic face) across the membrane. During the synthesis of ATP, protons flow in the reverse direction (down their electrochemical gradient) through ATP synthase (F0F1 complex), which protrudes in a knob at the cytosolic face in all cases.

Why is the mechanism of ATP synthesis shared among both prokaryotic organisms and eukaryotic organelles? Primitive aerobic bacteria were probably the progenitors of both mitochondria and chloroplasts in eukaryotic cells (see Figure 12-7). According to this endosymbiont hypothesis, the inner mitochondrial membrane was derived from the bacterial plasma membrane, with its cytosolic face pointing toward what became the matrix of the mitochondrion. Similarly, in plants, the progenitor bacterium’s plasma membrane became the chloroplast’s thylakoid membrane, and its cytosolic face pointed toward what became the stromal space of the chloroplast (chloroplast structure will be described in Section 12.6). In all cases, ATP synthase is positioned with the globular F1 domain, which catalyzes ATP synthesis, on the cytosolic face of the membrane, so ATP is always formed on the cytosolic face (see Figure 12-30). Protons always flow through ATP synthase from the exoplasmic to the cytosolic face of the membrane. This flow is driven by the proton-motive force. Invariably, the cytosolic face has a negative electric potential relative to the exoplasmic face.

In addition to ATP synthesis, the proton-motive force across the bacterial plasma membrane is used to power other processes, including the uptake of nutrients such as sugars (using proton/sugar symporters) and the rotation of bacterial flagella. Chemiosmotic coupling thus illustrates an important principle introduced in our discussion of active transport in Chapter 11: the membrane potential, the concentration gradients of protons (and other ions) across a membrane, and the phosphoanhydride bonds in ATP are equivalent and interconvertible forms of potential energy. Indeed, ATP synthesis through ATP synthase can be thought of as active transport in reverse.

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