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Appl Environ Microbiol. 1984 May; 47(5): 971–978. | PMCID: PMC240030 |
Methanosarcina acetivorans sp. nov., an Acetotrophic Methane-Producing Bacterium Isolated from Marine Sediments Kevin R. Sowers, Stephen F. Baron, and James G. Ferry* Department of Anaerobic Microbiology, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061 Abstract A new acetotrophic marine methane-producing bacterium that was isolated from the methane-evolving sediments of a marine canyon is described. Exponential phase cultures grown with sodium acetate contained irregularly shaped cocci that aggregated in the early stationary phase and finally differentiated into communal cysts that released individual cocci when ruptured or transferred to fresh medium. The irregularly shaped cocci (1.9 ± 0.2 mm in diameter) were gram negative and occurred singly or in pairs. Cells were nonmotile, but possessed a single fimbria-like structure. Micrographs of thin sections showed a monolayered cell wall approximately 10 nm thick that consisted of protein subunits. The cells in aggregates were separated by visible septation. The communal cysts contained several single cocci encased in a common envelope. An amorphous form of the communal cyst that had incomplete septation and internal membrane-like vesicles was also present in late exponential phase cultures. Sodium acetate, methanol, methylamine, dimethylamine, and trimethylamine were substrates for growth and methanogenesis; H2-CO2 (80:20) and sodium formate were not. The optimal growth temperature was 35 to 40°C. The optimal pH range was 6.5 to 7.0. Both NaCl and Mg2+ were required for growth, with maximum growth rates at 0.2 M NaCl and 0.05 M MgSO4. The DNA base composition was 41 ± 1% guanine plus cytosine. Methanosarcina acetivorans is the proposed species. C2A is the type strain (DSM 2834, ATCC 35395). Full text Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (2.7M), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References. Images in this article Click on the image to see a larger version. These references are in PubMed. This may not be the complete list of references from this article. - Balch WE, Fox GE, Magrum LJ, Woese CR, Wolfe RS. Methanogens: reevaluation of a unique biological group. Microbiol Rev. 1979 Jun;43(2):260–296. [PubMed]
- Balch WE, Wolfe RS. New approach to the cultivation of methanogenic bacteria: 2-mercaptoethanesulfonic acid (HS-CoM)-dependent growth of Methanobacterium ruminantium in a pressureized atmosphere. Appl Environ Microbiol. 1976 Dec;32(6):781–791. [PubMed]
- Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. [PubMed]
- Bryant MP. Commentary on the Hungate technique for culture of anaerobic bacteria. Am J Clin Nutr. 1972 Dec;25(12):1324–1328. [PubMed]
- Cappenberg TE, Prins RA. Interrelations between sulfate-reducing and methane-producing bacteria in bottom deposits of a fresh-water lake. 3. Experiments with 14C-labeled substrates. Antonie Van Leeuwenhoek. 1974;40(3):457–469. [PubMed]
- Conway de Macario E, Macario AJ, Wolin MJ. Specific antisera and immunological procedures for characterization of methanogenic bacteria. J Bacteriol. 1982 Jan;149(1):320–328. [PubMed]
- Jones JB, Bowers B, Stadtman TC. Methanococcus vannielii: ultrastructure and sensitivity to detergents and antibiotics. J Bacteriol. 1977 Jun;130(3):1357–1363. [PubMed]
- Jones William J, Paynter Malcolm J B. Populations of Methane-Producing Bacteria and In Vitro Methanogenesis in Salt Marsh and Estuarine Sediments. Appl Environ Microbiol. 1980 Apr;39(4):864–871. [PubMed]
- Kandler O, König H. Chemical composition of the peptidoglycan-free cell walls of methanogenic bacteria. Arch Microbiol. 1978 Aug 1;118(2):141–152. [PubMed]
- King Gary M, Klug MJ, Lovley DR. Metabolism of Acetate, Methanol, and Methylated Amines in Intertidal Sediments of Lowes Cove, Maine. Appl Environ Microbiol. 1983 Jun;45(6):1848–1853. [PubMed]
- King Gary M, Wiebe WJ. Tracer Analysis of Methanogenesis in Salt Marsh Soils. Appl Environ Microbiol. 1980 Apr;39(4):877–881. [PubMed]
- Laanbroek HJ, Pfennig N. Oxidation of short-chain fatty acids by sulfate-reducing bacteria in freshwater and in marine sediments. Arch Microbiol. 1981 Jan;128(3):330–335. [PubMed]
- Lovley Derek R, Klug Michael J. Intermediary Metabolism of Organic Matter in the Sediments of a Eutrophic Lake. Appl Environ Microbiol. 1982 Mar;43(3):552–560. [PubMed]
- Lovley Derek R, Klug Michael J. Sulfate Reducers Can Outcompete Methanogens at Freshwater Sulfate Concentrations. Appl Environ Microbiol. 1983 Jan;45(1):187–192. [PubMed]
- Martens Christopher S, Berner Robert A. Methane Production in the Interstitial Waters of Sulfate-Depleted Marine Sediments. Science. 1974 Sep 27;185(4157):1167–1169. [PubMed]
- Mink Ronald W, Dugan Patrick R. Tentative Identification of Methanogenic Bacteria by Fluorescence Microscopy. Appl Environ Microbiol. 1977 Mar;33(3):713–717. [PubMed]
- Mountfort Douglas O, Asher Rodney A. Role of Sulfate Reduction Versus Methanogenesis in Terminal Carbon Flow in Polluted Intertidal Sediment of Waimea Inlet, Nelson, New Zealand. Appl Environ Microbiol. 1981 Aug;42(2):252–258. [PubMed]
- Oremland Ronald S, Polcin Sandra. Methanogenesis and Sulfate Reduction: Competitive and Noncompetitive Substrates in Estuarine Sediments. Appl Environ Microbiol. 1982 Dec;44(6):1270–1276. [PubMed]
- Rivard Christopher J, Henson J Michael, Thomas Michael V, Smith Paul H. Isolation and Characterization of Methanomicrobium paynteri sp. nov., a Mesophilic Methanogen Isolated from Marine Sediments. Appl Environ Microbiol. 1983 Aug;46(2):484–490. [PubMed]
- Sansone Francis J, Martens Christopher S. Methane Production from Acetate and Associated Methane Fluxes from Anoxic Coastal Sediments. Science. 1981 Feb 13;211(4483):707–709. [PubMed]
- Schauer NL, Ferry JG. Metabolism of formate in Methanobacterium formicicum. J Bacteriol. 1980 Jun;142(3):800–807. [PubMed]
- Senior Eric, Lindström E Börje, Banat Ibrahim M, Nedwell David B. Sulfate Reduction and Methanogenesis in the Sediment of a Saltmarsh on the East Coast of the United Kingdom. Appl Environ Microbiol. 1982 May;43(5):987–996. [PubMed]
- Sørensen Jan, Christensen Dorte, Jørgensen Bo Barker. Volatile Fatty Acids and Hydrogen as Substrates for Sulfate-Reducing Bacteria in Anaerobic Marine Sediment. Appl Environ Microbiol. 1981 Jul;42(1):5–11. [PubMed]
- Sowers Kevin R, Ferry James G. Isolation and Characterization of a Methylotrophic Marine Methanogen, Methanococcoides methylutens gen. nov., sp. nov. Appl Environ Microbiol. 1983 Feb;45(2):684–690. [PubMed]
- Steensland H, Larsen H. A study of the cell envelope of the halobacteria. J Gen Microbiol. 1969 Mar;55(3):325–336. [PubMed]
- Weiss RL. Subunit cell wall of Sulfolobus acidocaldarius. J Bacteriol. 1974 Apr;118(1):275–284. [PubMed]
- Whitman WB, Ankwanda E, Wolfe RS. Nutrition and carbon metabolism of Methanococcus voltae. J Bacteriol. 1982 Mar;149(3):852–863. [PubMed]
- Winfrey Michael R, Ward David M. Substrates for Sulfate Reduction and Methane Production in Intertidal Sediments. Appl Environ Microbiol. 1983 Jan;45(1):193–199. [PubMed]
- WOLIN EA, WOLIN MJ, WOLFE RS. FORMATION OF METHANE BY BACTERIAL EXTRACTS. J Biol Chem. 1963 Aug;238:2882–2886. [PubMed]
- Zhilina TN, Zavarzin GA. Obrazovanie tsist metanosartsinoĭ. Mikrobiologiia. 1979 May–Jun;48(3):451–456. [PubMed]
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