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Thauer, R. , Jungerman, K. , and Decker, K. (1977). Energy conservation in chemotrophic anaerobic bacteria. Bacteriol. Rev. 41, 100-180. , and Kröger, A. (1981). The function of subunits of the fumarate reductase complex of Vibrio succinogenes. Biochim. Biophys. Acta 120, 577-584. , and Kröger, A. (1982). Reconstitution in liposomes of the electron transport chain catalyzing fumarate reduction by formate. Biochim. Biophys. Acta 682, 258-263. , and Kröger, A. (1986). Reconstitution of a functional electron transport chain from isolated enzymes in liposomes.

In addition to this system, the marine Vibrio has a respiration-driven Na + pump that directly generates ΔμΝ3+ especially at alkaline pH. The ΔμΝ3+ is utilized as a direct driving force for the solute transport and cell motility. The membrane of marine Vibrio contains H + translocating FjF^ATPase and ΔμΗ+ may be utilized for ATP synthesis. This organism also has substrate-level phosphorylation systems. The ΔμΝ3+-driven ATP synthesis was observed by Dibrov et al (1986b), but a Na + -dependent ATP synthase has not been identified.

1981). Molecular and enzymatic properties of cytochrome aa3-typc terminal oxidase derived from Nitrobacter agilis. J. Biochem. 89, 265-273. , and Yamanaka, T. (1985). Cytochrome aj of Nitrosomonas europea resembles aa3-type cytochrome c oxidase in many respects. Biochim. Biophys. Acta 810,174-183. Yang, T. (1986). Biochemical and biophysical properties of cytochrome o of Azotobacter vinelandii. Biochim. Biophys. Acta 848, 342-351. , and Trumpower, B. L. (1985). Purification of a three-subunit ubiquinolucytochrome c oxidoreductase complex from Paracoccus denitrificans.

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