Abstract
Respiratory and reverse electron transport by chemoautotrophic bacteria have been formulated in chemiosmotic terms. A thermodynamic analysis of this model, assuming equilibrium conditions, indicates that respiration by most chemoautotrophs can generate a protonmotive force easily sufficient to drive both ATP synthesis and reverse electron transport.
Similar content being viewed by others
References
Aleem MIH (1966) Generation of reducing power in chemosynthesis. II. Energy-linked reduction of pyridine nucleotides in the chemoautotroph Nitrosomonas europaea. Biochim Biophys Acta 113:216–224
Bowien B, Cook AM, Schlegel HG (1974) Evidence for the in vivo regulation of glucose 6-phosphate dehydrogenase activity in Hydrogenomonas eutropha H16 from measurements of the intra-cellular concentrations of metabolic intermediates. Arch Microbiol 97:273–281
Burton K, Wilson TH (1953) The free-energy changes for the reduction of diphosphopyridine nucleotide and the dehydrogenation of L-malate and L-glycerol-1-phosphate. Biochem J 54:86–94
Cox JC, Nicholls DG, Ingledew WJ (1979) Transmembrane electrical potential and transmembrane pH gradient in the acidophile Thiobacillus ferro-oxidans. Biochem J 178:195–200
Fillingame RH (1980) The proton-translocating pumps of oxidative phosphorylation. Ann Rev Biochem 49:1079–1113
Hollocher TC, Kumar S, Nicholas DJD (1982) Respiration-dependent proton translocation in Nitrosomonas europaea and its apparent absence in Nitrobacter agilis during inorganic oxidations. J Bacteriol 149:1013–1020
Matin A, Gottschal JC (1976) Influence of dilution rate on NAD(P) and NAD(P)H concentrations and ratios in a Pseudomonas sp. grown in continuous culture. J Gen Microbiol 94:333–341
Meyer O, Schlegel H-G (1980) Carbon monoxide: methylene blue oxidoreductase from Pseudomonas carboxydovorans. J Bacteriol 141:74–80
Mitchell P (1961) Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism. Nature 191:144–148
Mitchell P (1966) Chemiosmotic coupling in oxidative and photosynthetic phosphorylation. Glynn Research, Bodmin
Roth CW, Hempfling WP, Conners JN, Vishniac WV (1973) Thiosulfate- and sulfide-dependent pyridine nucleotide reduction and gluconeogenesis in intact Thiobacillus neapolitanus. J Bacteriol 114:592–599
Schneider K, Schlegel HG (1977) Localization and stability of hydrogenases from aerobic hydrogen bacteria. Arch Microbiol 112:229–238
Smith AJ, London J, Stanier RY (1967) Biochemical basis of obligate autotrophy in blue-green algae and thiobacilli. J Bacteriol 94:972–983
Thauer RK, Jungerman K, Decker K (1977) Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev 41:100–180
Wagman DD, Eans WH, Parker VB, Halow I, Bailey SM, Schum RH (1968) Selected values of chemical thermodynamic properties. Table for the first thirtyfour elements. Technical Note 270-3. U.S. Dept. of Commerce, National Bureau of Standards, Washington, DC
Wimpenny JWT, Firth A (1972) Levels of nicotinamide adenine dinucleotide and reduced nicotinamide adenine dinucleotide in facultative bacteria and the effect of oxygen. J Bacteriol 111:24–32
Author information
Authors and Affiliations
Additional information
Dedicated to the memory of Roger Stanier, who first called to my attention the problem discussed here; and whose analysis of the relationship between it and the phenomenon of “obligate” autotrophy (Smith et al. 1967), although later shown to be inadequate, remains for me a model of creative biochemical insight
Rights and permissions
About this article
Cite this article
Wheelis, M. Energy conservation and pyridine nucleotide reduction in chemoautotrophic bacteria: a thermodynamic analysis. Arch. Microbiol. 138, 166–169 (1984). https://doi.org/10.1007/BF00413017
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00413017