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Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids

III. Characterization of the filamentous gliding Desulfonema limicola gen. nov. sp. nov., and Desulfonema magnum sp. nov.

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Abstract

Gliding motility, ultrastructure and nutrition of two newly isolated filamentous sulfate-reducing bacteria, strains 5ac10 and 4be13, were investigated. The filaments were always attached to surfaces. Growth was supported by addition of insoluble aluminium phosphate or agar as substrata for gliding movement. Electron microscopy of ultrathin sections revealed cell walls characteristic of Gramnegative bacteria; the undulated structure of the outer membrane may pertain to the translocation mechanism. Intracytoplasmic membranes were present. Acetate, higher fatty acids, succinate or fumarate served as electron donors and carbon sources. Strain 5ac10 grew also with lactate, but not with benzoate that was used only by strain 4be13. Strain 5ac10 was able to grow slowly on H2 plus CO2 or formate in the presence of sulfate without additional organic carbon source. The capacity of complete oxidation was shown by stoichiometric measurements with acetate plus sulfate. Both strains contained b- and c-type cytochromes. Desulfoviridin was detected only in strain 5ac10. The two filamentous gliding sulfate reducers are described as new species of a new genus, Desulfonema limicola and Desulfonema magnum.

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References

  • Akagi JM, Adams V (1973) Isolation of a bisulfite reductase activity from Desulfotomaculum nigrificans and its identification as the carbon monoxide-binding pigment P582. J Bacteriol 116:392–396

    PubMed  Google Scholar 

  • Anderson RL, Ordal EJ (1961) Cytophaga succinicans sp. n., a facultatively anaerobic, aquatic myxobacterium. J Bacteriool 81:130–138

    Google Scholar 

  • Arlauskas J, Burchard RP (1982) Substratum requirements for bacterial gliding motility. Arch Microbiol 133:137–141

    Google Scholar 

  • Bachmann BJ (1955) Studies on Cytophaga fermentans, n. sp., a facultatively anaerobic lower myxobacterium. J Gen Microbiol 13:541–551

    PubMed  Google Scholar 

  • Bryant MP (1973) Nutritional requirements of the predominant rumen cellulolytic bacteria. Federation Proc 32:1809–1813

    Google Scholar 

  • Burchard RP (1980) Gliding motility of bacteria. BioScience 30:157–162

    Google Scholar 

  • Burchard RP (1981) Gliding motility of prokaryotes: ultrastructure, physiology, and genetics. Ann Rev Microbiol 35:497–529

    Google Scholar 

  • Burchard RP (1982a) Evidence for contractile flexing of the gliding bacterium Flexibacter FS-1. Nature 298:663–665

    PubMed  Google Scholar 

  • Burchard RP (1982b) Trail following by gliding bacteria. J Bacteriol 152:495–501

    PubMed  Google Scholar 

  • Castenholz RW (1973) Movements. In: Carr NG, Whitton BA (eds) The biology of blue-green algae. Blackwell Scientific Publications, Oxford London Edinburg Melbourne, pp 320–339

    Google Scholar 

  • Cline JD (1969) Spectrophotometric determination of hydrogen sulfide in natural waters. Limnol Oceanogr 14:454–458

    Google Scholar 

  • Costerton JWF, Murray RGE, Robinow CF (1961) Observations on the motility and the structure of Vitreoscilla. Can J Microbiol 7:329–339

    PubMed  Google Scholar 

  • Evans WC (1977) Biochemistry of the bacterial catabolism of aromatic compounds in anaerobic environments. Nature 270:17–22

    PubMed  Google Scholar 

  • Fenchel T (1969) The ecology of marine microbenthos. IV. Structure and function of the benthic ecosystem, its chemical and physical factors and the microfauna communities with special reference to the ciliated protozoa. Ophelia 6:1–182

    Google Scholar 

  • Ferry JG, Wolfe RS (1976) Anaerobic degradation of benzoate to methane by a microbial consortium. Arch Microbiol 107:33–40

    PubMed  Google Scholar 

  • Gräf W (1961) Anaerobe Myxobakterien, neue Mikroben in der menschlichen Mundhöhle. Arch Hyg Bakteriol 145:405–459

    PubMed  Google Scholar 

  • Güde H (1979) Grazing by protozoa as selection factor for activated sludge bacteria. Microbiol Ecol 5:225–237

    Google Scholar 

  • Halfen LN (1973) Gliding motility of Oscillatoria: ultrastructural and chemical characterization of the fibrillar layer. J Phycol 9:248–253

    Google Scholar 

  • Halfen LN, Castenholz RW (1971) Gliding motility in the blue-green alga, Oscillatoria princeps. J Phycol 7:133–145

    Google Scholar 

  • Hirsch P (1981) The family Pelonemataceae. In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The prokaryotes, vol I. Springer, Berlin Heidelberg New York, pp 412–421

    Google Scholar 

  • Holt SC, Leadbetter ER, Socransky SS (1979) Capnocytophaga: new genus of Gram-negative gliding bacteria. II. Morphology and ultrastructure. Arch Microbiol 122:17–27

    PubMed  Google Scholar 

  • Humphrey BA, Dickson MR, Marshall KC (1979) Physicochemical and in situ observations on the adhesion of gliding bacteria to surfaces. Arch Microbiol 120:231–238

    Google Scholar 

  • Keith CL, Bridges RL, Fina LR, Iverson KL, Cloran JA (1978) The anaerobic decomposition of benzoic acid during methane fermentation. IV. Dearomatization of the ring and volatile fatty acids formed on ring rupture. Arch Microbiol 118:173–176

    PubMed  Google Scholar 

  • Lapidus IR, Berg HC (1982) Gliding motility of Cytophaga sp. strain U67. J Bacteriol 151:384–398

    PubMed  Google Scholar 

  • Leadbetter ER, Holt SC, Socransky SS (1979) Capnocytophaga: new genus of Gram-negative gliding bacteria. I. General characteristics, taxonomic considerations and significance. Arch Microbiol 122:9–16

    PubMed  Google Scholar 

  • Newman MG, Socransky SS, Savitt ED, Propas DA, Crawford A (1976) Studies of the microbiology of periodontosis. J Periodontol 47:373–379

    PubMed  Google Scholar 

  • Nottingham PM, Hungate RE (1969) Methanogenic fermentation of benzoate. J Bacteriol 98:1170–1172

    PubMed  Google Scholar 

  • Pate JL, Chang L-YE (1979) Evidence that gliding motility in procaryotic cells is driven by rotary assemblies in the cell envelopes. Curr Microbiol 2:59–64

    Google Scholar 

  • Postgate JR (1959) A diagnostic reaction of Desulphovibrio desulphuricans. Nature 183:481–482

    Google Scholar 

  • Reichenbach H (1981) Taxonomy of the gliding bacteria. Ann Rev Microbiol 35:339–364

    Google Scholar 

  • Reichenbach H, Dworkin M (1981) Introduction to the gliding bacteria. In: Starr MP, Stolp H, Trüper HG, Balows A, Schlegel HG (eds) The prokaryotes, vol I. Springer, Berlin Heidelberg New York, pp 315–327

    Google Scholar 

  • Skuja J (1956) Taxonomische und biologische Studien über das Phytoplankton schwedischer Binnengewässer. Nova Acta Reg Soc Sci Upsal 16 No 3:1–104

    Google Scholar 

  • Skuja H (1974) Family Pelonemataceae. In: Buchanan RE, Gibbons NE (eds) Bergey's manual of determinative bacteriology, 8th ed. Williams & Wilkins, Baltimore, pp 122–127

    Google Scholar 

  • Strohl WR (1979) Ultrastructure of Cytophaga johnsonae and C. aquatilis by freeze-etching. J Gen Microbiol 112:261–268

    Google Scholar 

  • Strohl WR, Larkin JM (1978) Enumeration, isolation, and characterization of Beggiatoa from freshwater sediments. Appl Environ Microbiol 36:755–770

    Google Scholar 

  • Tarvin D, Buswell AM (1934) The methane fermentation of organic acids and carbohydrates. J Am Chem Soc 56:1751–1755

    Google Scholar 

  • Thauer RK (1982) Dissimilatory sulphate reduction with acetate as electron donor. Phil Trans R Soc Lond B298:467–471

    Google Scholar 

  • Trudinger PA (1970) Carbon monoxide-reacting pigment from Desulfotomaculum nigrificans and its possible relevance to sulfite reduction. J Bacteriol 104:158–170

    PubMed  Google Scholar 

  • Turekian KK (1969) The oceans, streams, and atmosphere. In: Wedepohl KH (ed) Handbook of geochemistry. Springer, Berlin Heidelberg New York, pp 295–323

    Google Scholar 

  • Veldkamp H (1961) A study of two marine agar-decomposing, facultatively anaerobic myxobacteria. J Gen Microbiol 26:331–342

    PubMed  Google Scholar 

  • Walther-Mauruschat A, Aragno M, Mayer F, Schlegel HG (1977) Micromorphology of Gram-negative hydrogen bacteria. II. Cell envelope, membranes, and cytoplasmic inclusions. Arch Microbiol 114:101–110

    PubMed  Google Scholar 

  • Weston JA, Knowles CJ (1973) A soluble CO-binding c-type cytochrome from the marine bacterium Beneckea natriegens. Biochim Biophys Acta 305:11–18

    PubMed  Google Scholar 

  • Widdel F (1983) Methods for enrichment and pure culture isolation of filamentos gliding sulfate-reducing bacteria. Arch Microbiol 134:282–285

    Google Scholar 

  • Widdel F, Pfennig N (1981) Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. I. Isolation of new sulfate-reducing bacteria enriched with acetate from saline environments. Description of Desulfobacter postgatei gen. nov., sp. nov. Arch Microbiol 129:395–400

    Google Scholar 

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Widdel, F., Kohring, GW. & Mayer, F. Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. Arch. Microbiol. 134, 286–294 (1983). https://doi.org/10.1007/BF00407804

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  • DOI: https://doi.org/10.1007/BF00407804

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