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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 122 (1979), S. 129-135 
    ISSN: 1432-072X
    Keywords: Anaerobic degradation ; Methanogenesis ; Sludge ; Syntrophic association ; H2 transfer ; Butyrate ; Propionate ; Acetate ; H2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A new species of anaerobic bacterium that degrades the even-numbered carbon fatty acids, butyrate, caproate and caprylate, to acetate and H2 and the odd-numbered carbon fatty acids, valerate and heptanoate, to acetate, propionate and H2 was obtained in coculture with either an H2-utilizing methanogen or H2-utilizing desulfovibrio. The organism could be grown only in syntrophic association with the H2-utilizer and no other energy sources or combination of electron donor and acceptors were utilized. It was a Gram-negative helical rod with 2 to 8 flagella, about 20 nm in diameter, inserted in a linear fashion about 130 nm or more apart along the concave side of the cell. It grew with a generation time of 84 h in co-culture with Methanospirillum hungatii and was present in numbers of at least 4.5×10-6 per g of anaerobic digestor sludge.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 133 (1982), S. 249-256 
    ISSN: 1432-072X
    Keywords: Anaerobic benzoate degrader ; Syntrophic association-Coculture ; Acetate production ; Methane production
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An anaerobic, motile, gram-negative, rod-shaped bacterium is described which degrades benzoate in coculture with an H2-utilizing organism and in the absence of exogenous electron acceptors such as O2, SO 4 = or NO 3 - . The bacterium was isolated from a municipal primary, anaerobic sewage digestor using anaerobic roll-tube medium with benzoate as the main energy source and in syntrophic association with an H2-utilizing sulfate-reducing Desulfovibrio sp. which cannot utilize benzoate or fatty acids apart from formate as energy source. The benzoate utilizer produced acetate (3 mol/mol of substrate degraded) and presumably CO2 and H2, or formate from benzoate. In media without sulfate and with Methanospirillum hungatei (a methanogen that utilizes only H2−CO2 or formate as the energy source) added, 3 mol of acetate and 0.7 mol of methane were produced per mol of benzoate and CO2 was probably formed. Low numbers of Desulfovibrio sp. were present in the methanogenic coculture and a pure coculture of the benzoate utilizer with M. hungatei was not obtained. The generation times for growth of the sulfate-reducing and methanogenic cocultures were 132 and 166h, respectively. The benzoate utilizer did not utilize other common aromatic compounds, C 3 - −C7 monocarboxylic acids, or C4-C6 dicarboxylic acids for growth, nor did it appear to use SO 4 = , NO 3 - or fumarate as alternative electron acceptors. Addition of H2 inhibited growth and benzoate degradation.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-072X
    Keywords: Thermophilic Methanocoecus ; Deep sea hydrothermal vent methanogen ; Plasmids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An extremely thermophilic methanogen was isolated from a hydrothermal vent core sample from Guaymas Basin, Gulf of California, at a depth of 2003 m. The isolate, designated strain AG86, was a coccoid autotroph using H2-CO2 as energy and carbon source with a growth temperature range of 48 to 92°C, optimum, 85°C. AG86 required NaCl and Mg2+ and trace amounts of selenite and tungstate. Vitamins were not required. However, yeast extract, Casamino acids and Trypticase stimulated growth significantly. When grown in the presence of these stimulants and at the optimal growth temperature and pH 6.5, the minimum doubling time was 20 min. Cells were fragile and readily lysed by detergents. The mol% G+C was 33%. These results and partial 16S rRNA sequencing indicated that AG86 belonged to the genus Methanococcus and closely resembled Methanococcus jannaschii. Tests for extrachromosomal DNA revealed a plasmid in AG86 and two plasmids in M. jannaschii. Different patterns were obtained from restriction endonuclease digestion of the three plasmids, and no homology was observed with DNA-DNA hybridization.
    Type of Medium: Electronic Resource
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