Abstract
From dilution series in defined mineral medium, a marine iregular coccoid methanogenic bacterium (strain MTP4) was isolated that was able to grow on methanethiol as sole source of energy. The strain also grew on dimethylsulfide, mono-, di-, and trimethylamine, methanol and acetate. On formate the organism produced methane without significant growth. Optimal growth on MT, with doubling times of about 20 h, occurred at 30°C in marine medium. The isolate required p-aminobenzoate and a further not identified vitamin. Strain MTP4 had a high tolerance to hydrogen sulfide but was very sensitive to mechanical forces or addition of detergents such as Triton X-100 or sodium dodecylsulfate. Methanethiol was fermented by strain MTP4 according to the following equation:
The growth yield was 3.06 g cell dry mass per mol of MT. During growth on MT the isolate released small amounts of DMS and, vice versa, degradation of DMS was accompanied by significant intermediate MT production.
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Abbreviations
- MT =:
-
methanethiol
- DMS =:
-
dimethylsulfide
References
Andreae MO, Barnard WR (1984) The marine chemistry of dimethylsulfide. Mar Chem 14: 267–279
Banwart WL, Bremner JM (1976) Evolution of volatile sulfur compounds from solids treated with sulfur containing organic materials. Soil Biol Biochem 8: 439–443
Clinde JD (1969) Spectrophotometric determination of hydrogen sulfide in natural waters. Limnol Oceanogr 14: 454–458
Kanagawa T, Kelly DP (1986) Breakdwon of dimethyl sulphide by mixed cultures and by Thiobacillus thioparus. FEMS Microbiol Lett 34: 13–19
Kiene RP (1986) Dimethyl sulfide metabolism in salt marsh sediments. FEMS Microbiol Ecol 53: 71–78
Kiene RP, Capone DG (1988) Microbial transformations of methylated sulfur compounds in anoxic saltmarsh sediments. Microbiol Ecol 15: 275–291
Kiene RP, Oremland RS, Catena A, Miller LM, Capone DG (1986) Metabolism of reduced methylated sulfur compounds in anaerobic sediments and by a pure culture of an estuarine methanogen. Appl Environ Microbiol 52: 1037–1037
Kiene RP, Visscher PT (1987) Production of methylated sulfur compounds from methionine an dimethylsulfoniopropionate in anoxic salt marsh sediments. Appl Environ Microbiol 53: 2426–2434
Kiene RP, Malloy KD, Taylor BF (1990) Sulfur-containing amino acids as precursors of thiols in anoxic coastal sediments. Appl Environ Microbiol 56: 156–161
King GM (1983) Utilization of hydrogen, acetate, and “noncompetitive” substrates by methanogenic bacteria in marine sediments. Geomicrobiol J 3: 275–306
King GM, Klug MJ, Lovley DR (1983) Metabolism of acetate, methanol, and methylated amines in intertidal sediments of Lowe's Cove, Maine Appl Environ Microbiol 43: 1848–1853
Lovelock JE, Maggs RJ, Rasmussen RA (1972) Atmospheric dimethylsulfide and the natural sulfur cycle. Nature 237: 452–453
Mathrani IM, Boone DR, Mah RA, Fox GE, Lau PP (1988) Methanohalophilus zhilinae sp. nov., an alkaliphilic, halophilic, methylotrophic methanogen. Int. J Sys Bacteriol 38: 139–142
Ni S, Boone DR (1991) Isolation and characterization of a dimethylsulfide-degrading methanogen, Methanolobus siciliae HI350, from an oil well, characterization of M. siciliae T4/MT, and emendation of M. siciliae. Int J Sys Bacteriol 41: 410–416
Oremland RS, Kiene RP, Mathrani I, Whiticar MJ, Boone DR (1989) Description of an estuarine methylotrophic methanogen which grows on dimethyl sulfide. Appl Environ Microbiol 55: 994–1002
Pfennig N, Wagener S (1986) An improved method for preparing wet mounts for photomicrographs of microorganisms. J Microbiol Methods 4: 303–306
Smith NA, Kelly DP (1988) Mechanism of oxidation of dimethyl disulphide by Thiobacillus thioparus strain E6. J Gen Microbiol 134: 3031–3039
Sowers KR, Ferry JG (1983) Isolation and characterization of a methylothrophic marine methanogen, Methanococcoides methylutens gen. nov., sp. nov. Appl Environ Microbiol 45: 684–690
Stetter KO (1989) Genus II. Methanolobus. In: Staley JT, Bryant MP, Pfennig N, Holt HG (eds) Bergey's manual of systematic bacteriology, vol 3. William & Wilkins, Baltimore, pp 2205–2207
Suylen GMH, Stefess GC, Kuenen JG (1986) Chemolithotrophic potential of a Hyphomicrobium species, capable of growth on methylated sulfur compounds. Arch Microbiol 146: 192–198
Widdel F, Bak F (1991) Gram-negative mesophilic sulfate-reducing bacteria. In: Balows A, Trüper HG, Dworkin M, Harder W, Schleifer KH (eds) The prokaryotes, 2nd ed, Vol IV, chapter 183. Springer-Verlag, New York pp 3352–3378
Widdel F (1988) Microbiology and ecology of sulfate- and sulfurreducing bacteria. In: Zehnder AJB (ed) Biology of anaerobic microorganisms. John Wiley & Sons. New York Chichester Brisbane, pp 469–585
Vogels GD, Keltjens JT, Drift Cvan der (1988) Biogeochemistry of methane production. In: Zehnder AJB (ed) Biology of anaerobic microorganisms. John Wiley & Sons, New York Chichester Brisbane, pp 707–770
Zinder SH, Brock TD (1978a) Methane, carbon dioxide, and hydrogen sulfide production from the terminal methiol group of methionine by anaerobic lake sediments. Appl Environ Microbiol 35: 344–352
Zinder SH, Brock TD (1978b) Production of methane and carbon dioxide from methane thiol and dimethyl sulphide by anaerobic lake sediments. Nature 279: 226–228
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Finster, K., Tanimoto, Y. & Bak, F. Fermentation of methanethiol and dimethylsulfide by a newly isolated methanogenic bacterium. Arch. Microbiol. 157, 425–430 (1992). https://doi.org/10.1007/BF00249099
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DOI: https://doi.org/10.1007/BF00249099