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4.5. References
Aitken, D.M., and Brown, A.D. 1969. Citrate and glyoxylate cycles in the halophil, Halobacterium salinarum. Biochim. Biophys. Acta 177: 351–354.
Alam, M., Lebert, M., Oesterhelt, D., and Hazelbauer, G.L. 1989. Methyl-accepting taxis proteins in Halobacterium halobium. EMBO J. 8: 631–640.
Altekar, W., and Rajagopalan, R. 1990. Ribulose bisphosphate carboxylase activity in halophilic Archaebacteria. Arch. Microbiol. 153: 169–174.
Altekar, W., and Rangaswamy, V. 1990. Induction of a modified EMP pathway for fructose breakdown in a halophilic archaebacterium. FEMS Microbiol. Lett. 69: 139–144.
Altekar, W., and Rangaswamy, V. 1991. Ketohexokinase (ATP: D-fructose 1-phosphotransferasc) initiates fructose breakdown via the modified EMP pathway in halophilic archaebacteria. FEMS Microbiol. Lett. 83:241–246.
Altekar, W., and Rangaswamy, V. 1992. Degradation of endogenous fructose during catabolism of sucrose and mannitol in halophilic archaebacteria. Arch. Microbiol. 158: 356–363.
Alvarez-Ossorio, M., Muriana, F.J.G., De La Rosa, F.F., and Relimpio, A.M. 1992. Purification and characterization of nitrate reductase from the halophile archaebacterium Haloferax mediterranei. Z. Naturforsch. 47c: 670–676.
Basinger, G.W., and Oliver, J.D. 1979. Inhibition of Halobacterium cutirubrum lipid biosynthesis by bacitracin. J. Gen. Microbiol. 111: 423–427.
Begonia, G.B., and Salin, M.L. 1991. Elevation of superoxide dismutase in Halobacterium halobium by heat shock. J. Bacteriol. 173: 5582–5584.
Bertrand, J.C., Almallah, M., Aquaviva, M., and Mille, G. 1990. Biodegradation of hydrocarbons by an extremely halophilic archaebacterium. Lett. Appl. Microbiol. 11: 260–263.
Bhaumik, S.R., and Sonawat, H.M. 1994. Pyruvate metabolism in Halobacterium salinarium studied by intracellular13C nuclear magnetic resonance spectroscopy. J. Bacteriol. 176: 2172–21
Bickel-Sandkötter, S., Gärtner, W., and Dane, M. 1996. Conversion of energy in halobacteria: ATP synthesis and phototaxis. Arch. Microbiol. 166: 1–11.
Bickel-Sandkötter, S., Wagner, V., and Schumann, D. 1998. ATP-synthesis in archaea: structure-function relations of the halobacterial A-ATPase. Photosynthesis Res. 57: 335–345.
Birkeland, N.K., and Ratkje, S.K. 1985. Active uptake of glutamate in vesicles of Halobacterium salinarium. Membr. Biochem. 6: 1–17.
Bolobova, A.V., Simankova, M.C., and Markovich, N.A. 1992. Cellulase complex of a new halophilic bacterium Halocella cellulolytica. Mikrobiologiya 61: 804–811 (Microbiology 61: 557–562).
Bonelo, G., Ventosa, A., Megías, M., and Ruiz-Berraquero, F. 1984. The sensitivity of halobacteria to antibiotics. FEMS Microbiol. Lett. 21: 341–345.
Bonet, M.L., and Schobert, B. 1992. The catalytic site is located on subunit I of the ATPase from Halobacterium saccharovorum — a direct photoaffinity labeling study. Eur. J. Biochem. 207: 369–376.
Bonora, P., Principi, H., Hochkoeppler, A., Borghese, R., and Zannoni, D. 1998. The respiratory chain of the halophilic anoxygenic purple bacterium Rhodospirillum sodomense. Arch. Microbiol. 170: 435–441.
Borowitzka, L.J. 1981. The microflora. Adaptations to life in extremely saline lakes. Hydrobiologia 81: 33–46.
Brandt, K.K., and Ingvorsen, K. 1997. Desulfobacter halotolerans sp. nov., a halotolerant acetate-oxidizing sulfate-reducing bacterium isolated from sediments of Great Salt Lake, Utah. Syst. Appl. Microbiol. 20: 366–373.
Bräsen, C., and Schönheit, P. 2001. Mechanisms of acetate formation and acetate activation in halophilic archaea. Arch. Microbiol. 175: 360–368.
Brooun, A., Zhang, W.S., and Alam, M. (1997) Primary structure and functional analysis of the soluble transducer protein HtrXI in the Archaeon Halobacterium salinarium. J. Bacteriol. 179: 2963–2968.
Brown-Peterson, N.J., and Salin, M.L. 1994. Salt stress in a halophilic bacterium: alterations in oxidative metabolism and oxy-intermediate scavenging systems. Can. J. Microbiol. 40: 1057–1063.
Brown-Peterson, N.J., Chen, H., and Salin, M.L. 1994. Enhanced superoxide production by membrane vesicles from Halobacterium halobium in a hyposaline environment. Biochem. Biophys. Res. Commun. 205: 1736–1740.
Brown-Peterson, N.J., Begonia, G.B., and Salin, M.L. 1995. Alterations in oxidative activity and superoxide dismutase in Halobacterium halobium in response to aerobic respiratory inhibitors. Free Radical Biol. Med. 18: 249–256.
Bykhovsky, V.Y.A., Pusheva, M.A., Zaitseva, N.I., Zhilina, T.N., Pankovskii, D.B., and Detkova, E.N. 1994. Biosynthesis of corrinoids and its possible precursors in extremely halophilic homoacetogenic bacterium Acetohalobium arabaticum gen. nov., sp. nov. Pritladnaya Mikrobiologiya Biochimiya 30: 93–103 (in Russian).
Cartení-Farina, M., Porcelli, M., Cacciapuoti, G., De Rosa, M., Gambacorta, A., Grant, W.D., and Ross, H.N.M. 1985. Polyamines in halophilic archaebacteria. FEMS Microbiol. Lett. 28: 323–327.
Caumette, P., Cohen, Y., and Matheron, R. 1990. Isolation and characterization of Desulfovibrio halophilus sp. nov., a halophilic sulfate-reducing bacterium isolated from Solar Lake (Sinai). Syst. Appl. Microbiol. 14: 33–38.
Cayol, J.-L., Fardeau, M.-L., Garcia, J.-L., and Ollivier, B. 2002. Evidence of interspecies hydrogen transfer from glycerol in saline environments. Extremophiles 6: 131–134.
Cheah, K.S. 1970. The membrane-bound ascorbate oxidase system of Halobacterium halobium. Biochim. Biophys. Acta 205: 148–160.
Chen, K.Y., and Martynowicz, H. 1984. Lack of detectable polyamines in an extremely halophilic bacterium. Biochem. Biophys. Res. Commun. 30: 423–429.
Chow, K.-C., and Mark, K.-K. 1980. Antibiotic susceptibility of Halobacterium cutirubrum. Microbios Lett. 15: 117–122.
Cimmino, C., Scoarughi, G.L., and Donini, P. 1993. Stringency and relaxation among the halobacteria. J. Bacteriol. 175: 6659–6662.
Conrad, R., Frenzel, P., and Cohen, Y. 1995. Methane emission from hypersaline microbial mats: lack of aerobic methane oxidation activity. FEMS Microbiol. Ecol. 16: 297–305.
Dane, M., Steinert, K., Esser, K., Bickel-Sandkötter, S., and Rodriguez-Valera, F. 1992. Properties of the plasma membrane ATPases of the halophilic archaebacteria Haloferax mediterranei and Haloferax volcanii. Z. Naturforsch. 47c: 835–844.
Danon, A., and Caplan, S.R. 1977. CO 2 fixation by Halobacterium halobium. FEBS Lett. 74: 255–258.
Dees, C., and Oliver, J.D. 1977. Growth inhibition of Halobacterium cutirubrum by cerulenin, a potent inhibitor of fatty acid synthesis. Biochem. Biophys. Res. Commun. 78: 36–44.
DeFrank, J.J., and Cheng, T.C. 1991. Purification and properties of an organophosphorus acid anhydrase from a halophilic bacterial isolate. J. Bacteriol. 173: 1938–1943.
DeFrank, J.J., Beaudry, W.T., Cheng, T.C., Harvey, S.P., Stroup, A.N., and Szafraniec, L.L. 1993. Screening of halophilic bacteria and Alteromonas species for organophosphorus hydrolyzing enzyme activity. Chem. Biol. Interact. 87: 141–148.
Del Moral, A., Roldan, E., Navarro, M., Monteoliva-Sanchez, M., and Ramos-Cormenzana, A. 1987. Formation of calcium carbonate crystals by moderately halophilic bacteria. Geomicrobiol. J. 5: 79–87.
Denda, K., Fujiwara, T., Seki, M., Yoshida, M., Fukumori, Y., and Yamanaka, T. 1991. Molecular cloning of the cytochrome aa 3 gene from the archaeon (archaebacterium) Halobacterium halobium. Biochem. Biophys. Res. Commun. 181: 316–322.
Dhar, N.M., and Altekar, W. 1986a. A class I (Schiff base) fructose-1,6-bisphosphate aldolase of halophilic archaebacterial origin. FEBS Lett. 199: 151–154.
Dhar, N.M., and Altekar, W. 1986b. Distribution of class I and class II fructose bisphosphate aldolases in halophilic archaebacteria. FEMS Microbiol. Lett. 35: 177–181.
Doronina, N.Y., and Trotsenko, Y.A. 1997. Aerobic methylotrophic bacterial communities of hypersaline ecosystems. Mikrobiologiya 66: 130–136 (Microbiology 66: 111–117).
Ducharme, L., Matheson, A.T., Yaguchi, M., and Visentin, L.P. 1972. Utilization of amino acids by Halobacterium cutirubrum in chemically defined medium. Can. J. Microbiol. 18: 1349–1351.
Dundas, I.E.D. 1977. Physiology of Halobacteriaceae. Adv. Microb. Physiol. 15: 85–120.
Dundas, I.D., and Halvorson, H.O. 1966. Arginine metabolism in Halobacterium salinarium, an obligately halophilic bacterium. J. Bacteriol. 91: 113–119.
Dundas, I.D., Srinivasan, V.R., and Halvorson, H.O. 1963. A chemically defined medium for Halobacterium salinarium strain I. Can. J. Microbiol. 9: 619–624.
Eddy, M.L., and Jablonski, P.E. 2000. Purification and characterization of a membrane-associated ATPase from Natronococcus occultus, a haloalkaliphilic archaeon. FEMS Microbiol. Lett. 189: 211–214.
Emerson, D., Chauhan, S., Oriel, P., and Breznak, J.A. 1994. Haloferax sp. D1227, a halophilic Archaeon capable of growth on aromatic compounds. Arch. Microbiol. 161: 445–452.
Ewersmeyer-Wenk, B, Zähner, H., Krone, B., and Zeeck, A. 1981. Metabolic products of microorganisms. 207. Haloquinone, a new antibiotic active against halobacteria. I. Isolation, characterization and biological properties. J. Antibiot. 34: 1531–1537.
Fernandez-Linares, L., Acquaviva, M., Bertrand, J.-C., and Gauthier, M. 1996. Effect of sodium chloride concentration on growth and degradation of eicosane by the marine halotolerant bacterium Marinobacter hydrocarbonoclasticus. Syst. Appl. Microbiol. 19: 113–121.
Ferrer, M.R., Quevedo-Sarmiento, J., Bejar, V., Delgado, R., Ramos-Cormenzana, A., and Rivadeneyra, M.A. 1988a. Calcium carbonate formation by Deleya halophila: effect of salt concentration and incubation temperature. Geomicrobiol. J. 6: 49–57.
Ferrer, M.R., Quevedo-Sarmiento, J., Rivadeneyra, M.A., Bejar, V., Delgado, R., and Ramos-Cormenzana, A. 1988b. Calcium carbonate precipitation by two groups of moderately halophilic microorganisms at different temperatures and salt concentrations. Curr. Microbiol. 17: 221–227.
Fischer, R.S., Bonner, C.A., Boone, D.R., and Jensen, R.A. 1993. Clues from a halophilic methanogen about aromatic amino acid biosynthesis in archaebacteria. Arch. Microbiol. 160: 440–446.
Fischer, M., Gokhman, I., Pick, U., and Zamir, A. 1996. A salt-resistant plasma membrane carbonic anhydrase is induced by salt in Dunaliella salina. J. Biol. Chem. 271: 17718–17723.
Fischer, M., Gokhman, I., Pick, U., and Zamir, A. 1997. A structurally novel transferrin-like protein accumulates in the plasma membrane of the unicellular green alga Dunaliella salina. J. Biol. Chem. 272: 1565–1570.
Fischer, M., Zamir, A, and Pick, U. 1998. Iron uptake by the halotolerant alga Dunaliella is mediated by a plasma membrane transferrin. J. Biol. Chem. 273: 17553–17558.
Flannery, W.L., and Kennedy, D.M. 1962. The nutrition of Vibrio costicola. I. A simplified synthetic medium. Can. J. Microbiol. 8: 923–928.
Forterre, P., Elie, C., and Kohiyama, M. 1984. Aphidicolin inhibits growth and DNA synthesis in halophilic archaebacteria. J. Bacteriol. 159: 800–802.
Franzmann, P.D., Stackebrandt, E., Sanderson, K., Volkmann, J.K., Cameron, D.E., Stevenson, P.L., McMeekin, T.A., and Burton, H.R. 1988. Halobacterium lacusprofundi sp. nov., a halophilic bacterium isolated from Deep Lake, Antarctica. Syst. Appl. Microbiol. 11: 20–27.
Fu, W., and Oriel., P. 1998. Gentisate 1,2-dioxygenase from Haloferax sp. D1227. Extremophiles 3: 45–53.
Fu, W., and Oriel, P. 1999. Degradation of 3-phenylpropionic acid by Haloferax sp. D1227. Extremophiles 2: 439–446.
Fujiwara,, T., Fukumori, Y., and Yamanaka, T. 1987. aa3-Type cytochrome c oxidase occurs in Halobacterium halobium and its activity is inhibited by higher concentrations of salts. Plant Cell Physiol. 28: 29–36.
Fujiwara, T., Fukumori, Y., and Yamanaka, T. 1989. Purification and properties of Halobacterium halobium “cytochromeaa3” which lacks CuA and CuB. J. Biochem. 105: 287–292.
Fujiwara, T., Fukumori, Y., and Yamanaka, T. 1993. Halobacterium halobium cytochrome b-558 and cytochrome b-562: purification and some properties. J. Biochem. 113: 48–54.
Fukumori, Y., Fujiwara, T., Okada-Takahashi, Y., Mukohata, Y., and Yamanaka, T. 1985. Purification and properties of a peroxidase from Halobacterium halobium L-33. J. Biochem. 98: 1055–1061.
Gauthier, M.J., Lafay, B., Christen, R., Fernandez, L., Acquaviva, M., Bonin, P., and Bertrand, J.-C. 1992. Marinobacter hydrocarbonoclasticus gen. nov., sp. nov., a new, extremely halotolerant, hydrocarbondegrading marine bacterium. Int. J. Syst. Bacteriol. 42: 568–576.
Ghosh, M., and Sonawat, H.M. 1998. Kreb’s cycle in Halobacterium salinarum investigated by 13 C nuclear magnetic resonance spectroscopy. Extremophiles 2: 427–433.
Giani, D., Giani, L., Cohen, Y., and Krumbein, W.E. 1984. Methanogenesis in the hypersaline Solar Lake (Sinai). FEMS Microbiol. Lett. 25: 219–224.
Gochnauer, M.B., and Kushner, D.J. 1969. Growth and nutrition of extremely halophilic bacteria. Can. J. Microbiol. 15: 1157–1165.
Grant, M.A., and Hochstein, L.I. 1984. A dissimilatory nitrite reductase in Paracoccus halodenitrificans Arch. Microbiol. 137: 79–84.
Grant, M.A., Cronin, S.E., and Hochstein, L.I. 1984. Solubilization and resolution of the membrane-bound nitrite reductase from Paracoccus halodenitrifricans into nitrite and nitric oxide reductases. Arch. Microbiol. 140: 183–186.
Grey, V.L., and Fitt, P.S. 1976. An improved synthetic growth medium for Halobacterium cutirubrum. Can. J. Microbiol. 22: 440–442.
Hallberg, C., and Baltscheffsky, H. 1979. Partial purification of membrane-bound b-type cytochrome from Halobacterium halobium. Acta Chem. Scand. B 33: 600–601.
Hallberg, C., and Baltscheffsky, H. 1981. Solubilization and separation of two b-type cytochromes from a carotenoid mutant of Halobacterium halobium. FEBS Lett. 125: 201–204.
Hallberg, C., and Hederstedt, L. 1981. Succinate dehydrogenase activity and succinate-reducible cytochrome in Halobacterium halobium. Acta Chem. Scand. B 35: 601–605.
Hallberg-Gradin, C., and Colmsjö, A. 1989, Four different b-type cytochromes in the halophilic archaebacterium, Halobacterium halobium. Arch. Biochem. Biophys. 272: 130–136.
Hamaide, F., Sprott, G.D., and Kushner, D.J. 1984a. Energetics of sodium-dependent α-aminoisobutyric acid transport in the moderate halophile Vibrio costicola. Biochim. Biophys. Acta 766: 77–87.
Hamaide, F., Sprott, G.D., and Kushner, D.J. 1984b. Energetic basis of development of salt-tolerant transport in a moderately halophilic bacterium, Vibrio costicola. Arch. Microbiol. 140:231–235.
Hamana, K. 1997. Polyamine distribution patterns within the families Aeromonadaceae, Vibrionaceae, Pasteurellaceae, and Halomonadaceae, and related genera of the gamma subclass of the Proteobacteria. J. Gen. Appl. Microbiol. 43: 49–59.
Hamana, K., Kamekura, M., Onishi, H., Akazawa, T., and Matsuzaki, S. 1985. Polyamines in photosynthetic eubacteria and extreme-halophilic archaebacteria. J. Biochem. 97: 1653–1658.
Hamana, K., Hamana, H., and Itoh, T. 1995. Ubiquitous occurrence of agmatine as the major polyamine within extremely halophilic archaebacteria. J. Gen. Appl. Microbiol. 41: 153–158.
Hartmann, R., Sickinger, H.-D., and Oesterhelt. D. 1980. Anaerobic growth of halobacteria. Proc. Natl. Acad. Sci. USA 77: 3821–3825.
Hartsel, S.C., Kolodziej, B.J., and Cassim, J.Y. 1988. Spectral evidence for cytochrome o in the brown membrane of Halobacterium halobium. Arch. Biochem. Biophys. 264: 74–81.
Hayes, V.E.A., Ternan, N.G., and McMullan, G. 2000. Organophosphonate metabolism by a moderately halophilic bacterial isolate. FEMS Microbiol. Lett. 186: 171–175.
Hildebrandt, P., Matysik, J., Schrader, B., Scharf, B., and Engelhard, M. 1994. Raman spectroscopic study of the blue copper protein halocyanin from Natronobacterium pharaonis. Biochemistry 33: 11426–11431.
Hilpert, R., Winter, J., Hammes, W., and Kandler, O. 1981. The sensitivity of archaebacteria to antibiotics. Zbl. Baktl. Hyg., 1 Abt. Orig. C 2: 11–20.
Hochman, A., Nissany, A., and Amizur, M. 1988. Nitrate reduction and assimilation by a moderately halophilic, halotolerant bacterium Ba 1 Biochim. Biophys. Acta 965: 82–89.
Hochstein, L.I. 1978. Carbohydrate metabolism in the extremely halophilic bacteria: the role of glucose in the regulation of citrate synthase activity, pp. 397–412 In: Caplan, S.R., and Ginzburg, M. (Eds.), Energetics and structure of halophilic microorganisms. Elsevier/North Holland Biomedical Press, Amsterdam.
Hochstein, L.I. 1988. The physiology and metabolism of the extremely halophilic bacteria, pp. 67–83 In: Rodriguez-Valera, F. (Ed.), Halophilic bacteria, Vol. II. CRC Press, Boca Raton.
Hochstein, L.I. 1991. Nitrate reduction in the extremely halophilic bacteria, pp. 129–137 In: Rodriguez-Valera. F. (Ed.), General and applied aspects of halophilic microorganisms. Plenum Press, New York.
Hochstein, L.I. 1992. ATP synthesis in Halobacterium saccharovorum: evidence that synthesis may be catalysed by and F 0 F 1 -ATP synthase. FEMS Microbiol. Lett. 97: 155–160.
Hochstein, L.I., and Lang, F. 1991. Purification and properties of a dissimilatory nitrate reductase from Haloferax denitrificans. Arch. Biochem. Biophys. 288: 380–385.
Hochstein, L.I., and Lawson, D. 1993. Is ATP synthesized by a vacuolar-ATPase in the extremely halophilic bacteria? Experientia 49: 1059–1063.
Hochstein, L.I., and Tomlinson, G.A. 1984. The growth of Paracoccus halodenitrificans in a defined medium. Can. J. Microbiol. 30: 837–840.
Hochstein, L.I., and Tomlinson, G.A. 1985. Denitrification by extremely halophilic bacteria. FEMS Microbiol. Lett. 27: 329–331.
Hochstein, L.I., Dalton, B.P., and Pollock, G. 1976. The metabolism of carbohydrates by extremely halophilic bacteria: identification of galactonic acid as a product of galactose metabolism. Can. J. Microbiol. 22: 1191–1196.
Hochstein, L.I., Kristjansson, H., and Altekar, W. 1987. The purification and subunit structure of a membranebound ATPase from the archaebacterium Halobacterium saccharovorum. Biochem. Biophys. Res. Commun. 147: 295–300.
Hochuli, M., Patzelt, H., Oesterhelt, D., Wüthrich, K., and Szyperski, T. 1999. Amino acid biosynthesis in the halophilic archaeon Haloarcula hispanica. J. Bacteriol. 181: 3226–3237.
Holmes, M.L., and Dyall-Smith, M.L. 1991. Mutations in DNA gyrase results in novobiocin resistance in halophilic archaebacteria. J. Bacteriol. 173: 642–648.
Hou, S., Larsen, R.W., Boudko, D., Riley, C.W., Karatan, E., Zimmer, M., Ordal, G.W., and Alam, M. 2000. Myoglobin-like aerotaxis transducers in Archaea and Bacteria. Nature 203: 540–544.
Hunter, M.I.S., and Millar, S.J.W. 1980. Effect of wall antibiotics on the growth of the extremely halophilic coccus, Sarcina marina NCMB 778. J. Gen. Microbiol. 120: 255–258.
Ihara, K., Abe, T., Sugimura, K.-I., and Mukohata, Y. 1992. Halobacterial A-ATP synthase in relation to VATPase. J. Exp. Biol. 172: 475–485.
Javor, B.J. 1983a. Planktonic standing crop and nutrients in a saltern ecosystem. Limnol. Oceanogr. 28: 153–159.
Javor, B.J. 1983b. Nutrients and ecology of the Western Salt and Exportadora de Sal saltern brines, pp. 195–205 In: 6th International symposium on salt, Vol. 1. Salt Institute, Toronto.
Javor, B.J. 1984. Growth potential of halophilic bacteria isolated from solar salt environments: carbon sources and salt requirements. Appl. Environ. Microbiol. 48: 352–360.
Javor, B.J. 1988. CO 2 fixation in halobacteria. Arch. Microbiol. 149: 433–440.
Jensen, R.A., d’Amato, T.A., and Hochstein, L.I. 1988. An extreme-halophile archaebacterium possesses the interlock type of prephenate dehydratase characteristic of the Gram-positive eubacteria. Arch. Microbiol. 148: 365–371.
Johnsen, U, Selig, M., Xavier, K.B., Santos, H., and Schönheit, P. 2001. Different glycolytic pathways for glucose and fructose in the halophilic archaeon Halococcus saccharolyticus. Arch. Microbiol. 175: 52–61.
Jolley, K.A., Maddocks, D.G., Gyles, S.L., Mullan, Z., Tang, S.-L., Dyall-Smith, M.L., Hough, D.W., and Danson, M.J. 2000. 2-Oxoacid dehydrogenase multienzyme complexes in the halophilic Archaea? Gene sequences and protein structural predictions. Microbiology UK 146: 1061–1069.
Kaidoh, K., Miyauchi, S., Abe, A., Tanabu, S., Nara, T., and Kamo, N. 1996. Rhodamine 123 efflux transporter in Haloferax volcanii is induced when cultured under ‘metabolic stress’ by amino acids: the efflux system resembles that in a doxorubicin-resistant mutant. Biochem. J. 314: 355–359.
Kalyuzhnaya, M.G., Khmelenina, V.N., Starostina, N.G., Baranova, S.B., Suzina, N.E., and Trotsenko, Y.A. 1998. A new moderately halophilic methanotroph of the genus Methylobacter. Mikrobiologiya 67: 532–539 (Microbiology 67: 438–444).
Kalyuzhnaya, M.G., Khmelenina, V.N., Suzina, N.E., Lysenko, A.M., and Trotsenko, Y.A. 1999. New methanotrophic isolates from soda lakes of the southeastern Transbaikal region. Mikrobiologiya 68: 677–685 (Microbiology 68: 592–600).
Kamekura, M., Wallace, R., Hipkiss, A.R., and Kushner, D.J. 1985. Growth of Vibrio costicola and other moderate halophiles in a chemically defined minimal medium. Can. J. Microbiol. 31: 870–872.
Kamekura, M., Bardocz, S., Anderson, P., Wallace, R., and Kushner, D.J. 1986. Polyamines in moderately and extremely halophilic bacteria. Biochim. Biophys. Acta 880: 204–208.
Karamanou, S., and Katinakis, P. 1988. Heat shock proteins in the moderately halophilic bacterium Deleya halophila: protective effect of high salt concentration against thermal shock. Ann. Microbiol. 139: 505–514.
Katinakis, P. 1989. The pattern of protein synthesis induced by heat-shock of the moderately halophilic bacterium Chromobacterium marismortui. protective effect of high salt concentration against the thermal shock. Microbiologica 12: 61–67.
Kauri, T., Wallace, R., and Kushner, D.J. 1990. Nutrition of the halophilic archaebacterium, Haloferax volcanii. Syst. Appl. Microbiol. 13: 14–18.
Kevbrin, V.V., and Zavarzin, G.A. 1992a. Methanethiol utilization and sulfur reduction by anaerobic halophilic saccharolytic bacteria. Curr. Microbiol. 24: 247–250.
Kevbrin, V.V., and Zavarzin, G.A. 1992b. Effect of sulfur compounds on the growth of the halophilic homoacetogenic bacterium Acetohalobium arabaticum. Mikrobiologiya 61: 812–817 (Microbiology 61: 563–567).
Kevbrin, V.V., Zhilina, T.N., and Zavarzin, G.A. 1995. Physiology of the halophilic homoacetic bacterium Acetohalobium arabaticum. Mikrobiologiya 64: 165–170 (Microbiology 64: 134–138).
Kevbrina, M.V., and Plakunov, V.K. 1992. Acetate metabolism in Natronococcus occultus. Mikrobiologiya 61: 770–775 (Microbiology 61: 534–538).
Kevbrina, M.V., Zvyagintseva, I.S., and Plakunov, V.K. 1989. The uptake of [14 C] acetate in Natronococcus occultus. Mikrobiologiya 58: 892–896 (Microbiology 58: 719–723).
Khmelenina, V.N., Starostina, N.G., Tsvetkova, M.G., Sokolov, A.P., Suzina, N.E., and Trotsenko, Y.A. 1996. Methanotrophic bacteria in saline reservoirs of Ukraina and Tuva. Mikrobiologiya 65: 696–703 (Microbiology 65: 609–615).
Khmelenina, V.N., Kalyuzhneya, M.G., Starostina, N.G., Suzina, N.E., and Trotsenko, Y.A. 1997. Isolation and characterization of halotolerant alkaliphilic methanotrophic bacteria from Tuva soda lakes. Curr. Microbiol. 35: 257–261.
Khmelenina, V.N., Kalyuzhnaya, M.G., Sakharovsky, V.G., Suzina, N.E., Trotsenko, Y.A., and Gottschalk, G. 1999. Osmoadaptation in halophilic and alkaliphilic methanotrophs. Arch. Microbiol. 172: 321–329.
Kneifel, H., Stetter, K.O., Andreesen, J.R., Wiegel, J., König, H., and Schoberth, S.M. 1986. Distribution of polyamines in representative species of archaebacteria. Syst. Appl. Microbiol. 7: 241–245.
Kokoeva, M.V., and Oesterhelt, D. 2000. BasT, a membrane-bound transducer protein for amino acid detection in Halobacterium salinarum. Mol. Microbiol. 35: 647–656.
Konishi, T., and Murakami, N. 1984. Detection of two DCCD binding components in the envelope membrane of H. halobium. FEBS Lett. 169: 283–296.
Koops, H.-P., and Möller, U. 1992. The lithotrophic ammonia-oxidizing bacteria, pp. 2625–2638 In: Balows, A., Trüper, H.G., Dworkin, M., Harder, W., and Schleifer, K.-H. (Eds.), The prokaryotes. A handbook on the biology of bacteria: ecophysiology, isolation, identification, applications. 2nd ed. Springer-Verlag, New York.
Koops, H.-P., Böttcher, B., Möller, U., Pommerening-Röser, A., and Stehr, G. 1990. Description of a new species of Nitrosococcus. Arch. Microbiol. 154: 244–248.
Krekeler, D., Sigalevich, P., Teske, A., Cypionka, H., and Cohen, Y. 1997. A sulfate-reducing bacterium from the oxic layer of a microbial mat from Solar Lake (Sinai), Desulfovibrio oxyclinae sp. nov. Arch. Microbiol. 167: 369–375.
Krishnan, G., and Altekar, W. 1991. An unusual class I (Schiff base) fructose-1,6-bisphosphate aldolase from the halophilic archaebacterium Haloarcula vallismortis. Eur. J. Biochem. 195: 343–350.
Kristjansson, H., and Hochstein, L.I. 1985. Dicyclohexylcarbodiimide-sensitive ATPase in Halobacterium saccharovorum. Arch. Biochem. Biophys. 241: 590–595.
Krone, B., Hinrichs, A., and Zeeck, A. 1981. Metabolic products of microorganisms. 208. Haloquinone, a new antibiotic active against halobacteria. II. Chemical structure and derivatives. J. Antibiot. 34: 1538–1543.
Kulichevskaya, I.S., Milekhina, E.I., Borezinkov, I.A., Zvyagintseva, I.S., and Belyaev, S.S. 1991. Oxidation of petroleum hydrocarbons by extremely halophilic archaehacteria. Mikrobiologiya 60: 860–866 (Microbiology 60: 596–601).
Kushner, D.J. 1993. Growth and nutrition of halophilic bacteria, pp. 87–103 In: Vreeland, R.H., and Hochstein, L.I. (Eds.), The biology of halophilic bacteria. CRC Press, Boca Raton.
Lai, M.-C., and Gunsalus, R.P. 1992. Glycine betaine and potassium ion are the major compatible solutes in the extremely halophilic methanogen Methanohalophilus strain Z7302. J. Bacteriol. 174: 7474–7477.
Lai, M., Sowers, K.R., Robertson, D.E., Roberts, M.F., and Gunsalus, R.P. 1991. Distribution of compatible solutes in the halophilic methanogenic archaebacteria. J. Bacteriol. 173: 5352–5358.
Lanyi, J.K., Renthal, R., and MacDonald, R.E. 1976. Light-induced glutamate transport in Halobacterium halobium envelope vesicles. II. Evidence that the driving force is a light-dependent sodium gradient. Biochemistry 15: 1603–1610.
Liaw, H.J., and Mah, R.A. 1992. Isolation and characterization of Haloanaerobacter chitinovorans gen. nov., sp. nov., a halophilic, anaerobic, chitinolytic bacterium from a solar saltern. Appl. Environ. Microbiol. 58: 260–266.
Lin, X., and White, R.H. 1987. Structure of sulfohalopterin-2 from Halobacterium marismortui. Biochemistry 26: 6211–6217.
Lin, X., and White, R.H. 1988. Distribution of charged pterins in nonmethanogenic archaebacteria. Arch. Microbiol. 150: 541–546.
Litchfield, C.D., Irby, A., and Vreeland, R.H. 1999. The microbial ecology of solar salt plants, pp. 39–52 In: Oren, A. (Ed.), Microbiology and biogeochemistry of hypersaline environments. CRC Press, Boca Raton.
Lobyreva, L.B., Ivashko, R.S., and Plakunov, V.K. 1991. Intracellular pool and transport of aromatic amino acids in Halobacterium salinarium cells. Mikrobiologiya 60: 227–231 (Microbiology 60: 149–152).
Lobyreva, L.B., Kokoeva, M.V., and Plakunov, V.K. 1994. Physiological role of tyrosine transport systems in Halobacterium salinarium. Arch. Microbiol. 162: 126–130.
Long, S., and Salin, M.L. 2000. Archaeal promoter-directed expression of the Halobacterium salinarum catalase-peroxidase gene. Extremophiles 4: 351–356.
MacDonald, R.E., and Lanyi, J.K. 1975. Light-induced transport in Halobacterium halobium envelope vesicles: a chemiosmotic system. Biochemistry 14: 2882–2889.
MacLeod, R.A. 1986. Salt requirements for membrane transport and solute retention in some moderate halophiles. FEMS Microbiol. Rev. 39: 109–113.
Majumdar, A., and Sonawat, H.M. 1998. A two-dimensional 1 H detected 13 C NMR investigation of pyruvate metabolism in Halobacterium salinarium. J. Biochem. 123: 115–119.
Maltseva, O., McGowan, C., Fulthorpe, R., and Oriel, P. 1996. Degradation of 2,4-dichlorophenoxyacetic acid by haloalkaliphilic bacteria. Microbiology UK 142: 1115–1122.
Mancinelli, R.L., and Hochstein, L.I. 1986. The occurrence of denitrification in extremely halophilic bacteria. FEMS Microbiol. Lett. 35: 55–58.
Mancinelli, R.L., Cronin, S., and Hochstein, L.I. 1986. The purification and properties of a cd-cytochrome nitrite reductase from Paracoccus halodenitrificans. Arch. Microbiol. 145: 202–208.
Mankin, A.S., and Garrett, R.A. 1991. Chloramphenicol resistance mutations in the single 23S rRNA gene of the archaeon Halobacterium halobium. J. Bacteriol. 173: 3559–3563.
Martin, E.L., Duryea-Rice, T., Vreeland, R.H., Hilsabeck, L., and Davis, C. 1983. Effects of NaCl on the uptake of α-[ 14 C]aminoisobutyric acid by the halotolerant bacterium Halomonas elongata. Can. J. Microbiol. 29: 1424–1429.
Martinez-Espinosa, R.M., Marhuenda-Egea, F.C., and Bonete, M.J. 2001. Purification and characterisation of a possible assimilatory nitrite reductase from the halophile archaeon Haloferax mediterranei. FEMS Microbiol. Lett. 196: 113–118.
Mattar, S., and Engelhard, M. 1997. Cytochrome ba 3 from Natronobacterium pharaonis — an archaeal four-subunit cytochrome-c type oxidase. Eur. J. Biochem. 250: 332–341.
Mattar, S., Scharf, B., Kent, S.B.H., Rodewald, K., Oesterhelt, D., and Engelhard, M. 1994. The primary structure of halocyanin, an archaeal blue copper protein, predicts a lipid anchor for membrane fixation. J. Biol. Chem. 269: 14939–14945.
Matveeva, N.I., Nikolaev, Y.A., and Plakunov, V.K. 1990. Dependence of transport of amino acids into cells of halophilic and halotolerant bacteria on NaCl content and osmolarity of the medium. Mikrobiologiya 59: 5–11 (Microbiology 59: 1–5).
May, B.P., and Dennis, P.P. 1987. Superoxide dismutase from the extremely halophilic archaebacterium Halobacterium cutirubrum. J. Bacteriol. 169: 1417–1422.
May, B.P., Tam, P., and Dennis, P.P. 1989. The expression of the superoxide dismutase gene in Halobacterium cutirubrum and Halobacterium volcanii. Can. J. Microbiol. 35: 171–175.
McMeekin, T.A., and Franzmann, P.D. 1988. Effect of temperature on the growth rates of halotolerant and halophilic bacteria isolated from Antarctic saline lakes. Polar Biol. 8: 281–285.
Meyer, T.E. 1985. Isolation and characterization of soluble cytochromes, ferredoxins and other chromophoric proteins from the halophilic phototrophic bacterium Ectothiorhodospira halophila. Biochim. Biophys. Acta 806: 175–183.
Meyer, T.E., Fitch, J.C., Bartsch, R.G., Tollin, G., and Cusanovich, M.A. 1990a. Soluble cytochromes and a photoactive yellow protein isolated from the moderately halophilic purple phototrophic bacterium, Rhodospirillum salexigens. Biochim. Biophys. Acta 1016: 364–370.
Meyer, T.E., Fitch, J.C., Bartsch, R.G., Tollin, G., and Cusanovich, M.A. 1990b. Unusual high redox potential ferredoxins and soluble cytochromes from the moderately halophilic purple phototrophic bacterium, Rhodospirillum salinarum. Biochim. Biophys. Acta 1017: 118–124.
Michel, H., and Oesterhelt, D. 1980. Electrochemical proton gradient across the cell membrane of Halobacterium halobium: effect of DCCD, relation to intracellular ATP, ADP and phosphate concentration, and influence of the potassium gradient. Biochemistry 19: 4607–4614.
Miyauchi, S., Komatsubara, M., and Kamo, K. 1992. In archaebacteria, there is a doxorubicin efflux pump similar to mammalian P-glycoprotein. Biochim. Biophys. Acta 1110: 144–150.
Miyauchi, S., Tanabu, S., Abe, A., Okumura, R., and Kamo, N. 1997. Culture in the presence of sugars increases activity of multi-drug efflux transporter on Haloferax volcanii. Microb. Drug Resist. 3: 359–363.
Moldoveanu, N., and Kates, M. 1989. Effect of bacitracin on growth and phospholipid, glycolipid and bacterioruberin biosynthesis in Halobacterium cutirubrum. J. Gen. Microbiol. 135: 2504–2508.
Monstadt, G.M., and Holldorf, A.M. 1991. Arginine deiminase from Halobacterium salinarum: purification and properties. Biochem. J. 273: 739–746.
Montalvo-Rodriguez, R., López-Garriga, J., Vreeland, R.H., Oren, A., Ventosa, A., and Kamekura, M. 2000. Haloterrigena thermotolerans sp. nov., a halophilic Archaeon from Puerto Rico. Int. J. Syst. Evol. Microbiol. 50: 1065–1071.
Montero, C.G., Ventosa, A., Rodriguez-Valera, F., Kates, M., Moldoveanu, N., and Ruiz-Berraquero, F. 1989. Halococcus saccharolyticus sp. nov., a new species of extremely halophilic non-alkaliphilic cocci. Syst. Appl. Microbiol. 12: 167–171.
Moschettini, G., Hochkoeppler, A., Monti, B., Benelli, B., and Zannoni, D. 1997. The electron transport system of the halophilic purple nonsulfur bacterium Rhodospirillum salinarum. 1. A functional and thermodynamic analysis of the respiratory chain in aerobically and photosynthetically grown cells. Arch. Microbiol. 168: 302–309.
Moschettini, G., Bonora, P., Zaccherini, E., Hochkoeppler, A., Principi, I., and Zannoni, D. 1999. The primary quinone acceptor and the membrane-bound c-type cytochromes of the halophilic purple nonsulftir bacterium Rhodospirillum salinarum: a spectroscopic and thermodynamic study. Photosyth. Res. 62: 43–53.
Mouné, S., Manac’h, M., Hirshler, A., Caumette, P., Willison, J.C., and Matheron, R. 1999. Haloanaerobacter salinarius sp. nov., a novel halophilic fermentative bacterium that reduces glycine-betaine to trimethylamine with hydrogen or serine as electron donors; emendation of the genus Haloanaerobacter. Int. J. Syst. Bacteriol. 49: 103–112.
Mukohata, Y., and Yoshida, M. 1987a. Activation and inhibition of ATPase synthesis in cell envelope vesicles of Halobacterium halobium. J. Biochem. 101:311–318.
Mukohata, Y., and Yoshida, M. 1987b. The H + -translocating ATP synthase in Halobacterium halobium differs from F 0 F 1 -ATPase/synthase. J. Biochem. 102: 797–802.
Mukohata, Y., Isoyama, M., and Fuke, A. 1986. ATP synthesis in cell envelope vesicles of Halobacterium halobium driven by membrane potential and/or base-acid transition. J. Biochem. 99: 1–8.
Mylona, P., and Katinakis, P. 1992. Oxidative stress in the moderately halophilic bacterium Deleya halophila: effect of NaCl concentration. Experientia 48: 54–57.
Nagata, Y., Tanaka, K., Iida, T., Kera, Y., Yamada, R., Nakajima, Y., Fujiwara, T., Fukumori, Y., Yamanaka, T., Koga, Y., Tsuji, S., and Kawaguchi-Nagata, K. 1999. Occurrence of D-amino acids in a few archaea and dehydrogenase activities in hyperthermophile Pyrobaculum islandicum. Biochim. Biophys. Acta 1435: 160–166.
Nanba, T., and Mukohata, Y. 1987. A membrane-bound ATPase from Halobacterium halobium: purification and characterization. J. Biochem. 102: 591–598.
Newton, G.L., and Javor, B. 1985. γ-Glutamylcysteine and thiosulfate are the major low-molecular-weight thiols in halobacteria. J. Bacteriol. 161: 438–441.
Ng, W.V., Kennedy, S.P., Mahairas, G.G., Berquist, B., Pan, M, Shukla, H.D., Lasky, S.R., Baliga, N.S., Thorsson, V., Sbrogna, J., Swartzell, S., Weir, D., Hall, J., Dahl, T.A., Welti, R., Goo, Y.A., Leithauser, B., Keller, K., Cruz, R., Danson, M.J., Hough, D.W., Maddocks, D.G., Jablonski, P.E., Krebs, M.P., Angevine, C.M., Dale, H., Isenberger, T.A., Peck, R.F., Pohlschroder, M., Spudich, J.L, Jong, K.-H., Alam, M., Freitas, T., Hou, S., Daniels, C.J., Dennis, P.P., Omer, A.D., Ebhardt, H., Lowe, T.M., Liang, P., Riley, M., Hood, L., and DasSarma, S. 2000. Genome sequence of Halobacterium species NRC-1. Proc. Natl. Acad. Sci. USA 97: 12176–12181.
Nikolayev, Y.A., and Matveyeva, N.I. 1990a. A comparative study of the energization of alanine transport in the moderately halophilic bacterium Vibrio costicola and in the halotolerant bacterium Micrococcus varians, at different pH. Mikrobiologiya 59: 933–937 (Microbiology 59: 643–646).
Nikolayev, Y.A., Matveyeva, N.I., and Plakunov, V.K. 1990b. Properties of amino acids transport systems in some weak and temperate halophiles and in halotolerant bacteria. Mikrobiologiya 59: 213–221 (Microbiology 59: 132–138).
Nissenbaum, A., Stiller, M., and Nishri, A. 1990. Nutrients in pore waters from Dead Sea sediments. Hydrobiologia 197: 83–90.
Oesterhelt, D. 1982. Anaerobic growth of halobacteria. Meth. Enzymol. 88: 417–420.
Oesterhelt, D., and Krippahl, G. 1983. Phototrophic growth of halobacteria and its use for isolation of photosynthetically-deficient mutants. Ann. Microbiol. 134B: 137–150.
Oh-Hama, T., Stolowich, N.J., and Scott, A.I. 1991. 5-Aminolevulinic acid biosynthesis in Propionibacterium shermanii and Halobacterium salinarium: distribution of the two pathways of 5-aminolevulinic acid biosynthesis in prokaryotes. J. Gen. Appl. Microbiol. 39: 513–519.
Ollivier, B., Hatchikian, C.E., Prensier, G., Guezennec, J., and Garcia, J.-L. 1991. Desulfohalobium retbaense gen. nov. sp. nov., a halophilic sulfate-reducing bacterium from sediments of a hypersaline lake in Senegal. Int. J. Syst. Bacteriol. 41: 74–81.
Ollivier, B., Caumette, P., Garcia, J.-L., and Mah, R.A. 1994. Anaerobic bacteria from hypersaline environments. Microbiol. Rev. 58: 27–38.
Ollivier, B., Fardeau, M.-L., Cayol, J.-L., Magot, M., Patel, B.K.C., Prensier, G., and Garcia, J.-L. 1998. Methanocalculus halotolerans gen. nov., sp. nov., isolated from an oil-producing well. Int. J. Syst. Bacteriol. 48:821–828.
Onishi, H., McCance, M.E., and Gibbons, N.E. 1965. A synthetic medium for extremely halophilic bacteria. Can. J. Microbiol. 11: 365–373.
Oremland, R.S., and King, G.M. 1989. Methanogenesis in hypersaline environments, pp. 180–190 In: Cohen, Y., and Rosenberg, E. (Eds.), Microbial mats. Physiological ecology of benthic microbial communities. American Society for Microbiology, Washington, DC.
Oremland, R.S., and Miller, L.G. 1993. Biogeochemistry of natural gases in three alkaline, permanently stratified (meromictic) lakes, pp. 439–452 In: Harwell, D. (Ed.), United States Geological Service professional paper 1570.
Oren, A. 1983a. Bacteriorhodopsin-mediated CO 2 photoassimilation in the Dead Sea. Limnol. Oceanogr. 28: 33–41.
Oren, A. 1983b. Clostridium lortetii sp. nov., a halophilic obligatory anaerobic bacterium producing endospores with attached gas vacuoles. Arch. Microbiol. 136: 42–48.
Oren, A. 1986. Intracellular salt concentration of the anaerobic halophilic eubacteria Haloanaerobium praevalens and Halobacteroides halobius. Can. J. Microbiol. 32: 4–9.
Oren, A. 1988. Anaerobic degradation of organic compounds at high salt concentrations. Antonie van Leeuwenhoek 54: 267–277.
Oren, A. 1990, Anaerobic degradation of organic compounds in hypersaline environments: possibilities and limitations, pp. 155–175 In: Wise, D.L. (Ed.), Bioprocessing and biotreatment of coal. Marcel Dekker, New York.
Oren, A. 1991. Anaerobic growth of halophilic archaeobacteria by reduction of fumarate. J. Gen. Microbiol. 137: 1387–1390.
Oren, A. 1993. Availability, uptake, and turnover of glycerol in hypersaline environments. FEMS Microbiol. Ecol. 12: 15–23.
Oren, A. 1994a. The ecology of the extremely halophilic archaca. FEMS Microbiol. Rev. 13: 415–440.
Oren, A. 1994b. Enzyme diversity in halophilic archaea. Microbiología SEM 10: 217–228.
Oren, A. 1995a. The role of glycerol in the nutrition of halophilic archaeal communities: a study of respirator, electron transport. FEMS Microbiol. Ecol. 16: 281–290.
Oren, A. 1995b. Uptake and turnover of acetate in hypersaline environments. FEMS Microbiol. Ecol. 18: 75–84.
Oren, A. 1996. Sensitivity of selected members of the Halobacteriaceae to quinolone antimicrobial compounds. Arch. Microbiol. 165: 354–358.
Oren, A. 1999. Bioenergetic aspects of halophilism. Microbiol. Mol. Biol. Rev. 63: 334–348.
Oren, A. 2001. The bioenergetic basis for the decrease in metabolic diversity at increasing salt concentrations: implications for the functioning of salt lake ecosystem. Hydrobiologia 466: 61–72.
Oren, A. 2002. Diversity of halophilic microorganisms: environments, phylogeny, physiology, and applications. J. Ind. Microbiol. Bioteclmol. 28: 56–63.
Oren, A., and Gurevich, P. 1994a. Distribution of glycerol dehydrogenase and glycerol kinase activity in halophilic archaea. FEMS Microbiol. Lett. 118: 311–316.
Oren, A., and Gurevich, P. 1994b. Production of D-lactate, acetate, and pyruvate from glycerol in communities of halophilic archaea in the Dead Sea and in saltern crystallizer ponds. FEMS Microbiol. Ecol. 14: 147–156.
Oren, A., and Gurevich, P. 1995a. Occurrence of the methylglyoxal bypass in halophilic Archaea. FEMS Microbiol. Lett. 125: 83–88.
Oren, A., and Gurevich, P. 1995b. Isocitrate lyase activity in halophilic archaea. FEMS Microbiol. Lett. 130: 91–95.
Oren, A., and Litchfield, C.D. 1999. A procedure for the enrichment and isolation of Halobacterium. FEMS Microbiol. Lett. 173: 353–358.
Oren, A., and Shilo, M. 1985. Factors determining the development of algal and bacterial blooms in the Dead Sea: a study of simulation experiments in outdoor ponds. FEMS Microbiol. Ecol. 31: 229–237.
Oren, A., and Trüper, H.G. 1990. Anaerobic growth of halophilic archaeobacteria by reduction of dimethylsulfoxide and trimethylamine N-oxide. FEMS Microbiol. Lett. 70: 33–36.
Oren, A., Pohla, H., and Stackebrandt, E. 1987. Transfer of Clostridium lortetii to a new genus Sporohalobacter gen. nov. as Sporohalobacter lortetii comb, nov., and description of Sporohalobacter marismortui sp. nov. Syst. Appl. Microbiol. 9: 239–246.
Oren, A., Gurevich, P., and Henis, Y. 1991. Reduction of nitrosubstituted aromatic compounds by the halophilic eubacteria Haloanaerobium praevalens and Sporohalobacter marismortui. Appl. Environ. Microbiol. 57: 3367–3370.
Oren, A., Gurevich, P., Azachi, M., and Henis, Y. 1992. Microbial degradation of pollutants at high salt concentrations. Biodegradation 3: 387–398.
Oren, A., Heldal, M., and Norland, S. 1997. X-ray microanalysis of intracellular ions in the anaerobic halophilic eubacterium Haloanaerobium praevalens. Can. J. Microbiol. 43: 588–592.
Oriel, P., Chauhan, S., Maltseva, O., and Fu, W. 1997. Degradation of aromatics and haloaromalics by halophilic bacteria, pp. 123–130 In: Horikoshi, K., Fukuda, M., and Kudo, T. (Eds.), Microbial diversity and genetics of biodegradation. Japan Scientific Societies Press, Tokyo/Karger, Basel.
Pecher, T., and Böck, A. 1981. In vivo susceptibility of halophilic and methanogenic organisms to protein synthesis inhibitors. FEMS Microbiol. Lett. 10: 295–297.
Pérez-Fillol, M., Rodríguez-Valera, F., and Ferry, J.G. 1985. Isolation of methanogenic bacteria able to grow in high salt concentration. Microbiología SEM 1: 29–33.
Pfeifer, F. 1988. Genetics of halobacteria, pp. 105–133 In: Rodriguez-Valera, F. (Ed.), Halophilic bacteria, Vol. II. CRC Press, Boca Raton.
Piatibratov, M., Hou, S., Broom, A., Yang, A., Yang, J., Chen, H., and Alam, M. 2000. Expression and fastflow purification of a polyhistidine-tagged myoglobin-like aerotaxis transducer. Biochim. Biophys. Ada 1524: 149–154.
Post, F.J. 1977. The microbial ecology of the Great Salt Lake. Microb. Ecol. 3: 143–165.
Post, F.J., and Stube, J.C. 1988. A microcosm study of nitrogen utilization in the Great Salt Lake, Utah. Hydrobiologia 158: 89–100.
Pusheva, M.A., and Detkova, E.N. 1996. Bioenergetic aspects of acetogenesis on various substrates by the extremely halophilic acetogenic bacterium Acetohalobium arabaticum. Mikrobiologiya 65: 589–593 (Microbiology 65: 516–520).
Pusheva, M.A., Detkova, E.N., Bolotina, N.P., and Zhilina, T.N. 1992. Properties of periplasmatic hydrogenase of Acetohalobium arabaticum, an extremely halophilic homoacetogenic bacterium. Mikrobiologiya 61: 933–938 (Microbiology 61: 653–657).
Pusheva, M.A., Pitryuk, A.V., Detkova, E.N., and Zavarzin, G.A. 1999a. Bioenergetics of acetogenesis in the extremely alkaliphilic homoacetogenic bacteria Natroniella acetigena and Natronoincola histidinivorans. Mikrobiologiya 68: 651–656 (Microbiology 68: 568–573).
Pusheva, M.A., Pitryuk, A.V., and Netrusov, A.I. 1999b. Inhibitory analysis of the energy metabolism of the extremely haloalkaliphilic homoacetogenic bacterium Natroniella acetigena. Mikrobiologiya 68: 647–650 (Microbiology 68: 565–567).
Rajagopalan, R., and Altekar, W. 1991. Products of non-reductive CO 2 assimilation in the halophilic archaebacterium Haloferax volcanii. Indian J. Biochem. Biophys. 28: 65–67.
Rajagopalan, R., and Altekar, W. 1994. Characterisation and purification of ribulose-bisphosphate carboxylase from heterotrophically grown halophilic archaebacterium, Haloferax mediterranei. Eur. J. Biochem. 221:863–869.
Ravot, G., Magot, M., Ollivier, B., Patel, B.K.C., Ageron, E., Grimont, P.A.D., Thomas, P., and Garcia, J.-L. 1997. Haloanaerobium congolense sp. nov., an anaerobic, moderately halophilic, thiosulfate-and sulfurreducing bacterium from an African oil field. FEMS Microbiol. Lett. 147: 81–88.
Rawal, N., Kelkar, S.M., and Altekar, W. 1988a. Alternative routes of carbohydrate metabolism in halophilic archaebacteria. Indian J. Biochem. Biophys. 25: 674–686.
Rawal, N., Kelkar, S.M., and Altekar, W. 1988b. Ribulose 1,5-bisphosphate dependent CO 2 fixation in the halophilic archaebacterium, Halobacterium mediterranei. Biochem. Biophys. Res. Commun. 156: 451–456.
Rengpipat, S., Lowe, S.E., and Zeikus, J.G. 1988. Effect of extreme salt concentrations on the physiology and biochemistry of Halobacteroides acetoethylicus. J. Bacteriol. 170: 3065–3071.
Rivadeneyra, M.A., Delgado, R., Quesada, E., and Ramos-Cormenzana, A. 1989. Does the high Mg 2+ content inhibit the CaCO 3 precipitation by Deleya halophila?, p. 418 In: Da Costa, M.S., Duarte, J.C., and Williams, R.A.D. (Eds.), Microbiology of extreme environments and its potential for biotechnology. Elsevier Applied Science, London.
Rivadeneyra, M.A., Delgado, R., Quesada, E., and Ramos-Cormenzana, A. 1991. Precipitation of calcium carbonate by Deleya halophila in media containing NaCl as sole salt. Curr. Microbiol. 22: 185–190.
Rivadeneyra, M.A., Delgado, R., del Moral, A., Ferrer, M.R., and Ramos-Cormenzana, A. 1994. Precipitation of calcium carbonate by Vibrio spp. from an inland saltern. FEMS Microbiol. Ecol. 13: 197–204.
Rivadeneyra, M.A., Ramos-Cormenzana, A., Delgado, G., and Delgado, R. 1996. Process of carbonate precipitation by Deleya halophila. Curr. Microbiol. 32: 308–313.
Rivaneneyra, M.A., Delgado, G., Ramos-Cormenzana, A., and Delgado, R. 1998. Biomineralization of carbonates by Halomonas eurihalina in solid and liquid media with different salinities: crystal formation sequence. Res. Microbiol. 149: 277–287.
Rivadeneyra, M.A., Delgado, G., Soriano, M., Ramos-Cormenzana, A., and Delgado, R. 1999. Biomineralization of carbonates by Marinococcus albus and Marinococcus halophilus isolated from the Salar de Atacama (Chile). Curr. Microbiol. 39: 53–57.
Rodriguez-Valera, F., Ruiz-Berraquero, F., and Ramos-Cormenzana, A. 1980. Isolation of extremely halophilic bacteria able to grow in defined inorganic media with single carbon sources. J. Gen. Microbiol. 119:535–538.
Rodriguez-Valera, F., Juez, G., and Kushner, D.J. 1983. Halobacterium mediterranei spec, nov., a new carbohydrate-utilizing extreme halophile. Syst. Appl. Microbiol. 4: 369–381.
Roeßler, M.,. and Müller, V. 1998. Quantitative and physiological analyses of chloride dependence of growth in Halobacillus halophilus. Appl. Environ. Microbiol. 64: 3813–3817.
Rubentschik, L. 1929. Zur Nitrifikation bei hohen Salzkonzentrationen. Zentralbl. Bakteriol. II Abt. 77: 1–18.
Rudolph, J., Nordmann, B., Storch, K.F., Gruenberg, H., Rodewald, K., and Oesterhelt, D. 1996. A family of halobacterial transducer proteins. FEMS Microbiol. Lett. 139: 161–168.
Ruepp, A., and Soppa, J. 1996. Fermentative arginine degradation in Halobacterium salinarium (formerly Halobacterium halobium): genes, gene products, and transcripts of the arcRACB gene cluster. J. Bacteriol. 178: 4942–4947.
Ruepp, A., Müller, H.N., Lottspeich, F., and Soppa, J. 1995. Catabolic ornithine transcarbamylase of Halobacterium halobium (salinarium): purification, characterization, sequence determination and evolution. J. Bacteriol. 177: 1129–1136.
Salin, ML., and Brown-Peterson, N.J. 1993. Dealing with active oxygen intermediates: a halophilic perspective. Experientia 49: 523–529.
Schäfer, G., Engelhard, M., and Müller, V. 1999. Bioenergetics of the archaea. Microbiol. Mol. Biol. Rev. 63: 570–620.
Scharf, B., and Engelhard, M. 1993. Halocyanin, an archaebacterial blue copper protein (type I) from Natronobacterium pharaonis. Biochemistry 32: 12894–12900.
Scharf, B., Wittenberg, R., and Engelhard, M. 1997. Electron transfer proteins from the haloalkaliphilic archaeon Natronobacterium pharaonis: possible components of the respiratory chain include cytochrome bc and a terminal oxidase cytochrome ba 3. Biochemistry 36: 4471–4479.
Schinzel, R., and Burger, K.J. 1984. Sensitivity of halobacteria to aphidicolin, an inhibitor of eukaryotic α-type DNA polymerases. FEMS Microbiol. Lett. 25: 187–190.
Schobert, B. 1991. F1-like properties of an ATPase from the archaebacterium Halobacterium saccharovorum. J. Biol. Chem. 266: 8008–8014.
Schobert, B. 1992. The binding of a second divalent metal ion is necessary for the activation of ATP hydrolysis and its inhibition by tightly bound ADP in the ATPase from Halobacterium saccharovorum. J. Biol. Chem. 267: 10252–10257.
Schobert, B., and Lanyi, J.K. 1989. Hysteretic behavior of an ATPase from the archaebacterium Halobacterium saccharovorum. J. Biol. Chem. 264: 12805–12812.
Senyushkin, A.A., Severina, L.O., and Zhilina, T.N. 1992. Influence of the environmental conditions on glucose transport in cells of halophilic anaerobic eubacteria of the genus Halobacteroides. Mikrobiologiya 60: 796–800 (Microbiology 60: 545–549).
Serrano, J.A., Camacho, M., and Bonete. M.J. 1998. Operation of glyoxylate cycle in halophilic archaea: presence of malate synthase and isocitrate lyase in Haloferax volcanii. FEBS Lett. 434: 13–16.
Serrano, J.A., and Bonete, M.J. 2001. Sequencing, phylogenetic and transcriptional analysis of the glyoxylate bypass operon (ace) in the halophilic archaeon Haloferax volcanii. Biochim. Biophys. Acta 1520: 154–162.
Severina, L.O., Senyushkin, A.A., and Zhilina, T.N. 1992. Glucose transport systems in halophilic anaerobic eubacteria of the genus Halobacteroides. Mikrobiologiya 61: 353–358 (Microbiology 61: 237–242).
Shand, R.F., and Perez, A.M. 1999. Haloarchaeal growth physiology, pp. 414–424 In: Seckbach, J. (Ed.), Enigmatic microorganisms and life in extreme environments. Kluwer Academic Publishers, Dordrecht.
Simankova, M.V., Chernych, N.A., Osipov, G.A., and Zavarzin, G.A. 1993. Halocella cellulolytica gen. nov., sp. nov., a new obligately anaerobic, halophilic, cellulolytic bacterium. Syst. Appl. Microbiol. 16: 385–389.
Sioud, M., Baldacci, G., Forterre, P., and de Recondo, A.-M. 1987. Antitumor drugs inhibit the growth of halophilic archaebacteria. Eur. J. Biochem. 169: 231–236.
Sioud, M., Possat, O., Elie, C., Siebold, L, and Forterre, P. 1988. Coumarin and quinolone action in archaebacteria: evidence for the presence of a DNA gyrase-like enzyme. J. Bacteriol. 170: 946–953
Skyring, G.W. 1988. Acetate as the main energy substrate for the sulfate-reducing bacteria in Lake Eliza (South Australia) hypersaline sediments. FEMS Microbiol. Lett. 53: 87–94.
Slobodkin, A.I., and Zavarzin, G.A. 1992. Methane production in halophilic cyanobacterial mats in lagoons of Sivash Lake. Mikrobiologiya 61: 294–298 (Microbiology 61: 198–201).
Sokolov, A.P., and Trotsenko, Y.A. 1995. Methane consumption in (hyper)saline habitats of Crimea (Ukraine). FEMS Microbiol. Ecol. 18: 299–304.
Sorokin, D., Tourova, T., Schmid, M.C., Wagner, M., Koops, H.-P., Kuenen, J.G., and Jetten, M. 2001. Isolation and properties of obligately chemolithoautotrophic and extremely alkali-tolerant ammoniaoxidizing bacteria from Mongolian soda lakes. Arch. Microbiol. 176: 170–177.
Sonawat, H.M., Srivasta, R., Swaminathan, S., and Govil, G. 1990. Glycolysis and Entner-Doudoroff pathways in Halobacterium halobium: Some new observations based on 13 C NMR spectroscopy. Biochem. Biophys. Res. Commun. 173: 358–362.
Sowers, K.R., Robertson, D.E., Noll, D., Gunsalus, R.P., and Roberts, M.F. 1990. NE-acctyl-β-lysine: an osmolyte synthesized by methanogenic archaebacteria. Proc. Natl. Acad. Sci. USA 87: 9083–9087.
Sreeramulu, K., Schmidt, C.L., Schäfer, G., and Anemüller, S. 1998. Studies on the electron transport chain of the euryarchaeon Halobacterium salinarum: indications for a type II NADH dehydrogenase and a complex III analog. J. Bioenerg. Biomembr. 30: 443–453.
Stan-Lotter, H., and Hochstein, L.I. 1989. A comparison of an ATPase from the archaebacterium Halobacterium saccharovorum with the F 1 moiety from the Escherichia coli ATP synthase. Eur. J. Biochem. 179: 155–160.
Stan-Lotter, H., Sulzner, M., Egelseer, E., Norton, C.F., and Hochstein, L.I. 1993. Comparison of membrane ATPases from extreme halophiles isolated from ancient salt deposits. Origins of Life and Evolution of the Biosphere 23: 53–64.
Steinert, K., and Bickel-Sandkötter, S. 1996, Isolation, characterization, and substrate specificity of the plasma membrane ATPase of the halophilic archaeon Haloferax volcanii. Z. Naturforsch. 51c: 29–39.
Steinert, K., Kroth-Pancic, P.G., and Bickel-Sandkötter, S. 1995. Nucleotide sequence of the ATPase A and B subunits of the halophilic archaebacterium Haloferax volcanii and characterization of the enzyme. Biochitn. Biophys. Acta 149: 137–144.
Steinert, K., Wagner, V., Kroth-Pancic, G., and Bickel-Sandkötter, S. 1997. Characterization and subunit structure of the ATP synthase of the halophilic archaeon Haloferax volcanii and organization of the ATP synthase genes. J. Biol. Chem. 272: 6261–6269.
Stephens, D.W., and D.M. Gillespie. 1976. Phytoplankton production in the Great Salt Lake, Utah, and a laboratory study of algal response to enrichment. Limnol. Oceanogr. 21: 74–87.
Stevenson, J. 1966. The specific requirement for sodium chloride for the active uptake of L-glutamate by Halobacterium salinarium. Biochem. J. 99: 257–260.
Storch, K.-F., Rudolph, J., and Oesterhelt, D. 1999. Car: a cytoptasmic sensor responsible for argininc chemotaxis in the archaeon Halobacterium salinarum. EMBO J. 18: 1146–1158.
Sulzner, M., Stan-Lotter, H., and Hochstein, L.I. 1992. Nucleotide protectable labeling of sulfhydryl groups in subunit I of the ATPase from Halobacterium saccharovorum. Arch. Biochem. Biophys. 296: 347–349.
Sundquist, A.R., and Fahey, R.C. 1988. The novel disulfide reductase bis-γ-glutamylcystine reductase and dihydrolipoamide dehydrogenase from Halobacterium halobium: purification by immobilized metal-ion affinity chromatography and properties of the enzymes. J. Bacteriol. 170: 3459–3467.
Sundquist, A.R., and Fahey, R.C. 1989. The function of γ-glutamylcysteine and bis-γ-glutamylcysteine reductase in Halobacterium halobium. J. Biol. Chem. 264: 719–725.
Switzer Blum, J., Stolz, J.F., Oren, A., and Oremland, R.S. 2001. Selenihalanaerobacter shriftii gen. nov., sp. nov., a halophilic anaerobe from Dead Sea sediments that respires selenate. Arch. Microbiol. 175: 208–219.
Sydow, U, Wohland, P., Wolke, I., and Cypionka, H. 2002. Bioenergetics of the alkaliphilic sulfate-redticing bacterium Desulfonatronovibrio hydrogenovorans. Microbiology UK 148: 853–860.
Takano, J., Kaidoh, K., and Kamo, N. 1995. Fructose transport by Haloferax volcanii. Can. J. Microbiol. 41: 241–246.
Takao, M., Kobayashi, T., Oikawa, A., and Yasui, A. 1989. Tandem arrangement of photolyase and superoxide dismutase genes in Halobacterium halobium. J. Bacteriol. 171: 6323–6329.
Tanaka, T., Burgess, J.G., and Wright, P.C. 2001. High-pressure adaptation by salt stress in a moderately halophilic bacterium obtained from open seawater. Appl. Microbiol. Biotechnol. 57: 200–204.
Tanaka, M., Ogawa, N., Ihara, K., Sugiyama, Y., and Mukohata, Y. 2002. Cytochrome aa 3 in Haloferax volcanii. J. Bacteriol. 184: 840–855.
Tawara, E., and Kamo, N. 1991. Glucose transport of Haloferax volcanii requires the Na + -electrochemical potential gradient and inhibitors for the mammalian glucose transporter inhibit the transport. Biochim. Biophys. Acta 1070: 293–299.
Ternan, N.G., and McMullan, G. 2002. Utilisation of aminomethane sulfonate by Chromohalobacter marismortui VH1. FEMS Microbiol. Lett. 207: 49–53.
Then, J., and Trüper, H.G. 1983. Sulfide oxidation in Ectothiorhodospira abdelmalekii. Evidence for the catalytic role of cytoclirome c-551. Arch. Microbiol. 135: 254–258.
Tindall, B.J. 1992. The family Halobacteriaceae, pp. 768–808. In: Balows, A., Trüper, H.G., Dworkin, M., Harder, W., and Schleifer, K.-H. (Eds.), The Prokaryotes. A handbook on the biology of bacteria: ecophysiology, isolation, identification, applications. Vol. I. Springer-Verlag, New York.
Tindall, B.J., and Trüper, H.G. 1986. Ecophysiology of the aerobic halophilic archaebacteria. Syst. Appl. Microbiol. 7: 202–212.
Tomlinson, G.A., and Hochstein, L.I. 1972a. Isolation of carbohydrate metabolizing, extremely halophilic bacteria. Can. J. Microbiol. 18: 698–701.
Tomlinson, G.A., and Hochstein, L.I. 1972b. Studies on acid production during carbohydrate metabolism by extremely halophilic bacteria. Can. J. Microbiol. 18: 1973–1976.
Tomlinson, G.A., and Hochstein, L.I. 1976. Halobacterium saccharovorum sp. nov., a carbohydratemetabolizing, extremely halophilic bacterium. Can. J. Microbiol. 22: 587–591.
Tomlinson, G.A., Koch, T.K., and Hochstein, L.I. 1974. The metabolism of carbohydrates by extremely halophilic bacteria: glucose metabolism via a modified Entner-Doudoroff pathway. Can. J. Microbiol. 20: 1085–1091.
Tomlinson, O.A., Strohm, M.P., and Hochstein, L.I. 1978. The metabolism of carbohydrates by extremely halophilic bacteria: the identification of lactobionic acid as a product of lactose metabolism by Halobacterium saccharovorum. Can. J. Microbiol. 24: 898–903.
Tomlinson, G.A., Jahnke, L.L., and Hochstein, L.I. 1986. Halobacterium denitrificans sp. nov., an extremely halophilic denitrifying bacterium. Int. J. Syst. Bacteriol. 36: 66–70.
Trotsenko, Y.A., and Khmelenina, V.N. 2002a. Biology of extremophilic and extremotolerant methanotrophs. Arch. Microbiol. 177: 123–131.
Trotsenko, Y.A., and Khmelenina, V.N. 2002b. The biology and osmoadaptation of haloalkaliphilic methanotrophs. Mikrobiologiya 71: 149–159 (Microbiology 71: 123–132).
Tsai, C.-R., Garcia, J.-L., Patel, B.K.C., Cayol, J.-L., Baresi, L, and Mah, R.A. 1995. Haloanaerobium alcaliphilum sp. nov., an anaerobic moderate halophile from the sediments of Great Salt Lake, Utah. Int. J. Syst. Bacteriol. 45: 301–307.
Ventosa, A, Nieto, J.J., and Oren, A. 1998. Biology of moderately halophilic aerobic bacteria. Microbiol. Mol. Biol. Rev. 62: 504–544.
Wais, A.C. 1988. Recovery of halophilic archaebacteria from natural environments. FEMS Microbiol. Ecol. 53: 211–216.
Wanner, C., and Soppa, J. 1999. Genetic identification of three ABC transporters as essential elements for nitrate respiration in Haloferax volcanii. Genetics 152: 1417–1428.
Welsh, D.T., Lindsay, Y.E., Caumette, P., Herbert, R.A., and Hannan, J. 1996. Identification of trehalose and glycine betaine as compatible solutes in the moderately halophilic sulfate reducing bacterium Desulfovibrio halophilus. FEMS Microbiol. Lett. 140: 203–207.
Wieland, F., Dompert, W., Bernhardt, G., and Sumper, M. 1980. Halobacterial glycoprotein saccharides contain covalently linked sulphate. FEBS Lett. 120: 110–114.
Wieland, F., Lechner, J., and Sumper, M. 1982. The cell wall glycoprotein of Halobacterium: structural, functional and biosynthetic aspects. Zbl. Bakt. Hyg. I Abt. Orig. C 3: 161–170.
Wood, A.P., and Kelly, D.P. 1991. Isolation and characterisation of Thiobacillus halophilus sp. nov., a sulphur-oxidising autotrophic eubacterium from a Western Australian hypersaline lake. Arch. Microbiol. 156: 277–280.
Zavarzin, G.A., Zhilina, T.N., and Pusheva, M.A. 1994. Halophilic acetogenic bacteria, pp. 432–444 In: Drake, H.L. (Ed.), Acetogenesis. Chapman & Hall, New York.
Zhang, W., Brooun, A., McCandless J., Banda, P., and Alam, M. 1996. Signal transduction in the Archaeon Halobacterium salinarium is processed through three subfamilies of 13 soluble and membrane-bound transducer proteins. Proc. Natl. Acad. Sci. USA 93: 4649–4654.
Zhilina, T.N., and Zavarzin, G.A. 1987. Methanohalobium evestigatus, gen. nov. sp. nov., the extremely halophilic methanogenic archaebacterium. Dokl. Akad. Nauk. SSSR 293: 464–468 (in Russian).
Zhilina, T.N., and Zavarzin, G.A. 1990a. A new extremely halophilic homoacetogenic bacterium Acetohalobium arabaticum gen. nov., sp. nov. Dokl. Akad. Nauk. SSSR 311: 745–747 (in Russian).
Zhilina, T.N., and Zavarzin, G.A. 1990b. Extremely halophilic, methylotrophic, anaerobic bacteria. FEMS Microbiol. Rev. 87: 315–322.
Zhilina, T.N., Miroshnikova, L.V., Osipov, G.A., and Zavarzin, G.A. 1992a. Halobacteroides lacunaris sp. nov., new saccharolytic, anaerobic, extremely halophilic organism from the lagoon-like hypersaline lake Chokrak. Mikrobiologiya 60: 714–724 (Microbiology 60: 495–503).
Zhilina, T.N., Zavarzin, G.A., Bulygina, E.S., Kevbrin, V.V., Osipov, G.A, and Chumakov, K.M. 1992b. Ecology, physiology and taxonomy studies on a new taxon of Haloanaerobiaceae, Haloincola saccharolytica gen. nov., sp. nov. Syst. Appl. Microbiol. 15: 275–284.
Zhilina, T.N., Zavarzin, G.A., Detkova, E.N., and Rainey, F.A. 1996. Natroniella acetigena gen. nov. sp. nov., an extremely haloalkaliphilic, homoacetic bacterium, a new member of Haloanaerobiales. Curr. Microbiol. 32: 320–326.
Zhilina, T.N., Tourova, T.P., Lysenko, A.M., and Kevbrin, V.V. 1997. Reclassification of Halobacteroides halobius Z-7287 on the basis of phylogenetic analysis as a new species Halobacteroides elegans sp. nov. Mikrobiologiya 66: 114–121 (Microbiology 66: 97–103).
Zoratti, M., and Lanyi, J.K. 1987. Phosphate transport in Halobacterium halobium depends on cellular ATP levels. J. Bacteriol. 169: 5755–5760.
Zvyagintseva, I.S., Belyaev, S.S., Borzenkov, I.A., Kostrikina, N.A., Mileklhina, E.I., and Ivanov, M.V. 1995a. Halophilic archaebacteria from the Kalamkass oil field. Mikrobiologiya 64: 83–87 (Microbiology 64: 67–71).
Zvyagintseva, I.S., Gerasimenko, L.M., Kostrikina, N.A., Bulygina, E.S., and Zavarzin, G.A. 1995b. Interaction of halobacteria and cyanobacteria in a halophilic cyanobacterial community. Mikrobiologiya 64: 252–258 (Microbiology 64: 209–214).
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(2003). Cellular Metabolism and Physiology of Hhalophilic Microorganisms. In: Halophilic Microorganisms and their Environments. Cellular Origin, Life in Extreme Habitats and Astrobiology, vol 5. Springer, Dordrecht. https://doi.org/10.1007/0-306-48053-0_5
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