The Bioenergetics of Alkalophilic Bacilli

References

• Garland P. B. Energy transduction and transmission in microbial systems. Symp. Soc. Gen. Microbiol. 1977; 27: 1
   Google Scholar
• Horikoshi K., Akiba T. Alkalophilic Microorganisms. Springer-Verlag, New York 1982
   Google Scholar
• Krulwich T. A. Bioenergetics of alkalophilic bacteria. J. Membr. Biol. 1986; 89: 113
   Google Scholar
• Krulwich T. A., Guffanti A. A. Physiology of acidophilic and alkalophilic bacteria. Adv. Microb. Physiol. 1983; 24: 173
   PubMedGoogle Scholar
• Guffanti A. A., Finkelthal O., Hicks D. B., Falk L., Sidhu A., Garro A., Krulwich T. A. Isolation and characterization of new facultatively alkalophilic strains of Bacillus. J. Bacteriol. 1986; 167: 766
   PubMedGoogle Scholar
• Mitchell P. Coupling of phosphorylation to electron and hydrogen transfer by a chemiosmotic type of mechanism. Nature (London) 1961; 191: 144
   PubMed Web of Science ®Google Scholar
• Harold F. M. The Vital Force: A Study of Bioenergetics. W. H. Freeman, New York 1986
   Google Scholar
• Krulwich T. A. The fine structure of obligately alkalophilic bacilli. FEMS Microbiol. Lett. 1982; 13: 299
   Google Scholar
• Koga Y., Nishihara M., Morii H. Lipids of alkalophilic bacteria: identification, composition and metabolism. J. Univ. Occup. Environ. Health 1982; 4: 227
   Google Scholar
• Clejan S., Krulwich T. A., Mondrus K. R., Seto-Young D. Membrane lipid composition of obligately and facultatively alkalophilic strains of Bacillus spp. J. Bacteriol. 1986; 168: 334
   Google Scholar
• Nishihara M., Morii H., Koga Y. Bis(monoacyl glycerophosphate in alkalophilic bacteria. J. Biochem. 1982; 92: 1469
   Google Scholar
• Taylor R. F. Bacterial triterpenoids. Microbiol. Rev. 1984; 48: 181
   Google Scholar
• Ourisson G., Rohmer M., Poralla K. Prokaryotic hopanoids and other polyterpenoid sterol surrogates. Annu. Rev. Microbiol. 1987; 41: 301
   PubMed Web of Science ®Google Scholar
• Rohmer M., Bouvier P., Ourisson G. Molecular evolution of biomembranes: structural equivalents and phylogenetic precursors of sterols. Proc. Natl. Acad. Sci. U.S.A. 1979; 76: 847
   PubMed Web of Science ®Google Scholar
• Bisserat P., Wolff G., Albrecht A.-M., Tanaka T., Nakatani Y., Ourisson G. A direct study of the cohesion of lecithin bilayers: the effect of hopanoids and α,ω-dihydroxycarotenoids. Biochem. Biophys. Res. Commun. 1983; 110: 320
   Google Scholar
• Kannenberg E., Blume A., McElhaney R. N., Poralla K. Monolayer and calorimetric studies of phosphatidylcholines containing branched-chain fatty acids and of their interactions with cholesterol and with a bacterial hopanoid in model membranes. Biochim. Biophys. Acta 1983; 733: 111
   Web of Science ®Google Scholar
• Milon A., Lazrak T., Albrecht A.-M., Wolff G., Weill G., Ourisson G., Nakatani Y. Osmotic swelling of unilamellar vesicles by the stopped-flow light scattering method, influence of vesicle size, solute, temperature, cholesterol and three α,ω-dihydroxycarotenoids. Biochim. Biophys. Acta 1986; 859: 1
   Google Scholar
• Rilfors L., Khan A., Brentel I., Wieslander A., Lindblom G. Cubic liquid crystalline phase with phosphatidyl-ethanolamine from Bacillus megaterium containing branched acyl chains. FEBS Lett. 1982; 149: 293
   Google Scholar
• Verkleij A. J. Lipidic intramembranous particles. Biochim. Biophys. Acta 1984; 779: 43
   PubMed Web of Science ®Google Scholar
• De Krruijff B., Cullis P. R. Cytochrome c specifically induces nonbilayer structures in cardiolipin-containing model membranes. Biochim. Biophys. Acta 1980; 602: 477
   Google Scholar
• Koyama N., Takinishi H., Nosoh Y. A possible relation of membrane proteins to the alkalostability of a fundamentally alkalophilic Bacillus. FEMS Microbiol. Lett. 1983; 16: 213
   Google Scholar
• Kitada M., Krulwich T. A. Purification and characterization of the cytochrome oxidase from alkalophilic Bacillus firmus RAB. J. Bacteriol. 1984; 158: 963
   Google Scholar
• Davidson M. W., Gray K. A., Knaff D. B., Krulwich T. A. Purification and characterization of two soluble cytochromes from the alkalophile Bacillus firmus RAB. Biochim. Biophys. Acta
   Google Scholar
• Krulwich T. A., Agus R., Schneier M., Guffanti A. A. The buffering capacity of bacilli that grow in different ranges of pH. J. Bacteriol. 1985; 162: 768
   PubMed Web of Science ®Google Scholar
• Kitada M., Guffanti A. A., Krulwich T. A. Bioenergetic properties and viability of the alkalophilic Bacillus firmus RAB as a function of pH and Na+ content of the medium. J. Bacteriol. 1982; 152: 1096
   Google Scholar
• Lewis R. J., Krulwich T. A., Reynafarje B., Lehninger A. L. Respiration-dependent proton translocation in alkalophilic Bacillus firmus RAB and its non-alkalophilic mutant derivative. J. Biol. Chem. 1983; 258: 2109
   Google Scholar
• Clejan S., Krulwich T. A. Permeability of cells and liposomes from facultatively and obligately alkalophilic strains of. Bacillus, 9th Int. Biophys. Congr. IUPAB, Jerusalem 1987; 208
   Google Scholar
• Lewis R. J., Belkina S., Krulwich T. A. Alkalophiles have much higher cytochrome contents than conventional bacteria and than their own non-alkalophilic mutant derivatives. Biochem. Biophys. Res. Commun. 1980; 95: 857
   Google Scholar
• Lewis R. J., Prince R., Dutton P. L., Knaff D., Krulwich T. A. The respiratory chain of Bacillus alcalophilus and its non-alkalophilic mutant derivative. J. Biol Chem. 1981; 256: 10543
   Google Scholar
• Kitada M., Lewis R. J., Krulwich T. A. The respiratory chain of the alkalophilic bacterium Bacillus firmus RAB and its non-alkalophilic mutant derivative. J. Bacteriol. 1983; 154: 330
   Google Scholar
• Guffanti A. A., Susman P., Blanco R., Krulwich T. A. The protonmotive force and α-aminoisobutyric acid transport in an obligately alkalophilic bacterium. J. Biol. Chem. 1978; 253: 708
   Google Scholar
• Tokuda H., Unemoto T. Characterization of the respiration-dependent Na+ pump in the marine bacterium Vibrio alginolyticus. J. Biol. Chem. 1982; 257: 10007
   Google Scholar
• Tokuda H., Udagawa T., Unemoto T. Generation of the electrochemical potenital of Na+ by the Na+-motive NADH oxidase in inverted membrane vesicles of Vibrio alginolyticus. FEBS Lett. 1985; 183: 95
   Google Scholar
• Ken-Dror S., Preger R., Avi-Dor Y. Functional characterization of the uncoupler-insenstive Na+ pump of the halotolerant bacterium, Ba1. Arch. Biochem. Biophys. 1986; 244: 122
   Google Scholar
• Hayashi M., Unemoto T. Subunit component and their roles in the sodium-transport NADH:quinone reductase of a marine bacterium. Vibrio alginolyticus, Biochim. Biophys. Acta 1987; 890: 47
   Google Scholar
• Sugiyama S., Matsukura H., Imae Y. Relationship between Na+-dependent cytoplasmic pH homeostasis and Na+-dependent flagellar rotation and amino acid transport in alkalophilic Bacillus. Biochim. Biophys. Acta 1986; 852: 38
   Google Scholar
• Koyama N., Nosoh Y. Effect of potassium and sodium ions on the cytoplasmic pH of an alkalophilic Bacillus. Biochim. Biophys. Acta 1985; 812: 206
   Google Scholar
• Sugiyama S., Matsukura H., Imae Y. Relationship between Na+-dependent cytoplasmic pH homeostasis and Na+-dependent flagellar rotation and amino acid transport in alkalophilic Bacillus. FEBS Lett. 1985; 182: 265
   Google Scholar
• Hirota N., Imae Y. Na+-driven flagellar motors of an alkalophilic Bacillus strain YN-1. J. Biol. Chem. 1983; 258: 10577
   Google Scholar
• Kitada M., Horikoshi K. Bioenergetic properties of alkalophilic Bacillus sp. strain C-59 on an alkaline medium containing K2CO3. J. Bacteriol. 1987; 169: 5761
   Google Scholar
• Krulwich T. A., Guffanti A. A., Bornstein R. F., Hoffstein J. A sodium requirement for growth, solute transport, and pH homeostasis in Bacillus firmus RAB. J. Biol. Chem. 1982; 257: 1885
   Google Scholar
• Krulwich T. A., Guffanti A. A., Fong M. Y., Falk L., Hicks D. B. Alkalophilic Bacillus firmus RAB generates variants which can grow at lower Na+ concentrations than the parental strain. J. Bacteriol. 1986; 165: 884
   Google Scholar
• Kitada M., Wijayanti L., Horikoshi K. Biochemical properties of a thermophilic alkalophile. Agric. Biol. Chem. 1987; 51: 2429
   Web of Science ®Google Scholar
• Krulwich T. A., Federbush J. G., Guffanti A. A. Presence of a nonmetabolizable solute that is translocated with Na+ enhances Na+-dependent pH homeostasis in an alkalophilic Bacillus. J. Biol. Chem. 1985; 260: 4055
   Google Scholar
• Koyama N., Ishikawa Y., Nosoh Y. Dependence of the growth of pH-sensitive mutants of a facultatively alkalophilic Bacillus on the regulation of cytoplasmic pH. FEMS Microbiol. Lett. 1986; 34: 195
   Google Scholar
• McLaggan D., Selwyn M. J., Dawson A. P. Dependence on Na+ of control of cytoplasmic pH in a facultative alkalophile. FEBS Lett. 1984; 165: 254
   Google Scholar
• Zilberstein D., Agmon V., Schuldiner S., Padan E. The sodium/proton antiporter is part of the pH homeostasis mechanism in Escherichia coli. J. Biol. Chem. 1982; 257: 3687
   Google Scholar
• Ishikawa T., Hama H., Tsuda M., Tsuchiya T. Isolation and properties of a mutant of Escherichia coli possessing defective Na+/H+ antiporter. J. Biol. Chem. 1987; 262: 7443
   Google Scholar
• Goldberg E. B., Arbel T., Chen J., Karpel R., Mackie G. A., Schuldiner S., Padan E. Characterization of a Na+/H+ antiporter gene of Escherichia coli. Proc. Natl. Acad. Sci. USA. 1987; 84: 2615
   Google Scholar
• MacNab R. M., Castle A. M. A variable stoichiometry model for pH homeostasis in bacteria. Biophys. J. 1987; 52: 637
   Google Scholar
• Garcia M. L., Guffanti A. A., Krulwich T. A. Characterization of the Na+/H+ antiporter of alkalophiic bacilli in vivo: Δ±-dependent 22Na+ efflux from whole cells. J. Bacteriol. 1983; 156: 1151
   Google Scholar
• Bassilana M., Dramiano E., Leblanc G. Kinetic properties of Na+-H+ antiport in Escherichia coli membrane vesicles: effects of imposed electrical potential, proton gradient and internal pH. Biochemistry 1984; 23: 5288
   Google Scholar
• Mandel K. G., Guffanti A. A., Krulwich T. A. Monovalent cation/proton antiporters in membrane vesicles from Bacillus alcalophilus. J. Biol. Chem. 1980; 255: 7391
   Google Scholar
• Guffanti A. A. ATP-dependent Na+/H+ antiport activity in Bacillus alcalophilus requires generation of an electrochemical gradient of protons. FEMS Microbiol. Lett. 1983; 17: 307
   Google Scholar
• Seto- Young D., Garcia M. L., Krulwich T. A. Reconstitution of a bacterial Na+/H+ antiporter. J. Biol. Chem. 1985; 260: 11393
   Google Scholar
• Nakamura T., Hsu C.-M., Rosen B. P. Cation/proton antiport systems in Escherichia coli. J. Biol. Chem. 1986; 261: 678
   Google Scholar
• Booth I. R., Kroll R. G. Regulation of cytoplasmic pH (pHin) in bacteria and its relationship to metabolism. Biochem. Soc. Trans. 1983; 11: 29
   Google Scholar
• Lanyi J. K. The role of Na+ in transport processes of bacterial membranes. Biochim. Biophys. Acta 1979; 559: 377
   PubMedGoogle Scholar
• Ohta K., Kiyomiya A., Koyama N., Nosoh Y. The basis of the alkalophilic property of a species of Bacillus. J. Gen. Microbiol. 1975; 86: 259
   Google Scholar
• Koyama N., Kiyomiya A., Nosoh Y. Na+-dependent uptake of amino acids by an alkalophilic Bacillus. FEMS Microbiol. Lett. 1976; 72: 77
   Google Scholar
• Kitada M., Horikoshi K. Sodium ion-stimulated ‘1-14C’-aminoisobutyric acid uptake in alkalophilic Bacillus species. J. Bacteriol. 1977; 131: 784
   Google Scholar
• Guffanti A. A., Blanco R., Benenson R. A., Krulwich T. A. Bioenergetic properties of alkaline-tolerant and alkalophilic strains of Bacillus firmus. J. Gen. Microbiol. 1980; 119: 79
   Google Scholar
• Kitada M., Horikoshi K. Further properties of sodium ion stimulated ‘l-14C’ aminoisobutyric acid uptake in alkalophilic Bacillus No. 8–1. J. Biochem. 1980; 87: 1279
   Google Scholar
• Kitada M., Horikoshi K. Sodium ion-stimulated amino acid uptake in membrane vesicles of alkalophilic Bacillus No. 8–1. J. Biochem. 1980; 88: 1757
   Google Scholar
• Bonner S., Mann M. J., Guffanti A. A., Krulwich T. A. Na+/solute symport in membrane vesicles from Bacillus alcalophilus. Biochim. Biophys. Acta 1982; 679: 315
   Google Scholar
• Ando A., Yabuki M., Kusaka I. Na+-driven Ca++ transport in alkalophilic Bacillus. Biochim. Biophys. Acta 1981; 640: 179
   Google Scholar
• Ando A., Irie S., Masuda L. M., Matsushita T., Fujii T., Yabuki M., Kusaka I. H+- or K+- dependent transport systems of phosphate in alkalophilic Bacillus. Biochim. Biophys. Acta 1983; 734: 290
   Google Scholar
• Guffanti A. A., Blanco R., Krulwich T. A. A requirement for ATP for B-galactoside transport by Bacillus alcalophilus. J. Biol. Chem. 1979; 254: 1033
   Google Scholar
• Kitada M., Horikoshi K. Alkaline protease production from methylacetate by alkalophilic Bacillus sp. J. Fermentation Technol. 1976; 54: 383
   Google Scholar
• Guffanti A. A., Eisenstein H. C. Purification and characterization of flagella from the alkalophilic Bacillus firmus RAB. J. Gen. Microbiol. 1983; 129: 3239
   Google Scholar
• Hirota N., Kitada M., Imae Y. Flagellar motors of alkalophilic Bacillus are powered by an electrochemical potential gradient of Na+. FEBS Lett. 1981; 132: 278
   Web of Science ®Google Scholar
• Chernyak B. V., Dibrov P. A., Glagolev A. N., Sherman M. Y., Skulachev V. P. A novel type of energetics in a marine alkali-tolerant bacterium: Δ±Na+-driven motility and sodium cycle. FEBS Lett. 1983; 164: 38
   Google Scholar
• Dibrov P. A., Kostyrko V. A., Lasarova R. L., Skulachev V. P., Smirnova I. A. The sodium cycle. I. Na+-dependent motility and modes of membrane energization in the marine alkalotolerant Vibrio alginolyticus. Biochim. Biophys. Acta 1986; 850: 449
   Google Scholar
• Koyama N., Koshiya K., Nosoh Y. Purification and properties of ATPase from an alkalophilic Bacillus. Arch. Biochem. Biophys. 1980; 199: 103
   Google Scholar
• Hicks D. B., Krulwich T. A. The membrane ATPase of alkalophilic Bacillus firmus RAB is an F1-type ATPase. J. Biol. Chem. 1986; 261: 12896
   Google Scholar
• Foster D. L., Fillingame R. H. Stoichiometry of subunits in the H+-ATPase complex of Escherichia coli. J. Biol. Chem. 1982; 257: 2009
   Google Scholar
• Saraste M., Gay N. H., Eberle A., Runswick M. J., Walker J. E. The ATP operon: nucleotide sequence of the genes for the α,β, and γ subunits of Escherichia coli ATP synthase. Nucleic Acids Res. 1981; 9: 5287
   PubMedGoogle Scholar
• Hicks D. B., Krulwich T. A. Purification and characterization of the F1 ATPase from Bacillus subtilis and its uncoupler-resistant mutant derivatives. J. Bacteriol. 1987; 169: 4743
   Google Scholar
• Hochman Y., Carmeli C. Correlation between the kinetics of activation and inhibition of adenosine triphosphatase activity by divalent metal cations and the binding of manganese to chloroplast coupling factor 1. Biochemistry 1981; 20: 6287
   Google Scholar
• Carper S. W., Lancaster J. R., Jr. An electrogenic sodium-translocating ATPase in Methanococcus voltae. FEBS Lett. 1986; 200: 177
   Google Scholar
• Dharmavaram R. M., Konisky J. Identification of a vanadate-sensitive, membrane-bound ATPase in the archaebacterium Methanococcus voltae. J. Bacteriol. 1987; 169: 3921
   Google Scholar
• Kinoshita N., Unemoto T., Kobayashi H. Sodium-stimulated ATPase in Streptococcus faecalis. J. Bacteriol. 1984; 158: 844
   Google Scholar
• Hilpert W., Schink B., Dimroth P. Life by a new decarboxylation-dependent energy conservation mechanism with Na+ as coupling ion. EMBO J. 1984; 3: 1665
   PubMed Web of Science ®Google Scholar
• Laubinger W., Dimroth P. Characterization of the Na+-stimulated ATPase of Propionigenium modestum as an ezyme of the F1F0 type. Eur. J. Biochem. 1987; 168: 475
   Google Scholar
• Skulachev V. P. Membrane-linked energy transductions. Bioenergetic functions of sodium: H+ is not unique as coupling ion. Eur. J. Biochem. 1985; 151: 199
   Google Scholar
• Dibrov P. A., Lazarova R. L., Skulachev V. P., Verkhovskaya M. L. The sodium cycle. II. Na+-coupled oxidative phosphorylation in Vibrio alginolyticus cells. Biochim. Biophys. Acta 1986; 850: 458
   Google Scholar
• Tokuda H., Unemoto T. Growth of a marine Vibrio alginolyticus and moderately haiophilic V. costicola becomes uncoupler resistant when the respiration-dependent Na+ pump functions. J. Bacteriol. 1983; 156: 636
   Google Scholar
• Hamaide F., Kushner D., Sprott G. D. Protonmotive force and Na+/H+ antiport in a moderate halophile. J. Bacteriol. 1983; 156: 537
   Google Scholar
• Kakinuma Y., Unemoto T. Sucrose uptake is driven by the Na+ electrochemical potential in the marine bacterium Vibrio alginolyticus. J. Bacteriol. 1985; 163: 1293
   Google Scholar
• Buchanan R. E., Gibbons N. E. Bergey's Manual of Determinative Bacteriology8th ed. Williams & Wilkins, Baltimore 1975
   Google Scholar
• Tokuda H., Unemoto T. Na+ is translocated at NADH:quinone oxidoreductase segment in the respiratory chain of Vibrio alginolyticus. J. Biol. Chem. 1984; 259: 7785
   Google Scholar
• Unemoto T., Hayashi M., Hayashi M. Na+ dependent activation of NADH oxidase in membrane fractions from haiophilic Vibrio alginolyticus and V. costicolus. J. Biochem. 1977; 82: 1389
   Google Scholar
• Tokuda H., Unemoto T. A respiration-dependent primary sodium extrusion system functioning at alkaline pH in the marine bacterium Vibrio alginolyticus. Biochem. Biophys. Res. Commun. 1981; 102: 265
   Google Scholar
• Nakumura T., Tokuda H., Unemoto T. K+/H+ antiporter functions as a regulator of cytoplasmic pH in a marine bacterium. Vibrio alginolyticus, Biochim. Biophys. Acta 1984; 776: 330
   Google Scholar
• Guffanti A. A., Fuchs R. T., Schneier M., Chiu E., Krulwich T. A. A transmembrane electrical potential generated by respiration is not equivalent to a diffusion potential of the same magnitude for ATP synthesis by Bacillus firmus RAB. J. Biol. Chem. 1984; 259: 2971
   Google Scholar
• Guffanti A. A., Chiu E., Krulwich T. A. Failure of an alkalophilic bacterium to synthesize ATP in response to a valinomycin-induced potassium diffusion potential at high pH. Arch. Biochem. Biophys. 1985; 239: 327
   Google Scholar
• Guffanti A. A., Bornstein R. F., Krulwich T. A. Oxidative phosphorylation by membrane vesicles from Bacillus alcalophilus. Biochim. Biophys. Acta 1981; 635: 619
   Google Scholar
• Ferguson S. J., Sorgato M. C. The phosphorylation potential generated by respiring bovine heart submitochondrial particles. Biochem. J. 1977; 168: 299
   Google Scholar
• Ferguson S. J. Fully delocalized chemiosmotic or localized proton flow pathways in energy coupling? A scrutiny of the experimental evidence. Biochim. Biophys. Acta 1985; 811: 47
   Google Scholar
• Williams R. J. P. Possible functions of chains of catalysts. J. Theor. Biol. 1961; 1: 1
   Google Scholar
• Rottenberg H. Proton-coupled energy conservation: chemiosomotic and intramembrane coupling. Mod. Cell Biol. 1985; 4: 47
   Google Scholar
• Westerhoff H. V., Melandri B. A., Venturoli G., Azzone G. F., Kell D. B. A minimal hypothesis for membrane-linked free energy transduction: the role of independent, small coupling units. Biochim. Biophys. Acta 1984; 768: 257
   PubMed Web of Science ®Google Scholar
• Hicks D. B., unpublished
   Google Scholar
• Clejan S., unpublished
   Google Scholar
• Clejan S., Krulwich T. A., unpublished
   Google Scholar
• Seto-Young D., unpublished
   Google Scholar
• Hicks D., unpublished
   Google Scholar
• Guffanti A., unpublished
   Google Scholar