United States Geological Survey, 345 Middlefield Road, Menlo Park, California 94025; University of Georgia Marine Institute, Sapelo Island, Georgia 31327 ; School of Public Health, University of California, Los Angeles, Los Angeles, California 90024 ; Federal Institute for Geosciences and Natural Resources, D-3000 Hannover 51, Hannover, Federal Republic of Germany ; and Department of Environmental Science and Engineering, Oregon Graduate Center, Beaverton, Oregon 97006-1999.
Appl Environ Microbiol. 1989 Apr;55(4):994-1002. doi: 10.1128/aem.55.4.994-1002.1989.
Characteristics of an obligately methylotrophic coccoid methanogen (strain GS-16) previously isolated from estuarine sediment are described. Growth was demonstrated on dimethyl sulfide (DMS) or trimethylamine (TMA), but not on methane thiol, methane thiol plus hydrogen, dimethyl disulfide, or methionine. DMS-grown cells were able to metabolize DMS and TMA simultaneously when inoculated into media containing substrate levels of these compounds. However, TMA-grown cells could not metabolize [C]DMS to CH(4), although they could convert [C]methanol to CH(4). These results suggest that metabolism of DMS proceeds along a somewhat different route than that of TMA and perhaps also that of methanol. The organism exhibited doubling times of 23 and 32 h for growth (25 degrees C) in mineral media on TMA and DMS, respectively. Doubling times were more rapid ( approximately 6 h) when the organisms were grown on TMA in complex broth. In mineral media, the fastest growth on DMS occurred between pH levels of 7.0 and 8.7, at 29 degrees C, and with 0.2 to 0.4 M Na and 0.04 M Mg. Somewhat different results occurred for growth on TMA in complex broth. Cells had a moles percent G+C value of 44.5% for their DNA. Growth on DMS, TMA, and methanol yielded stable carbon isotope fractionation factors of 1.044, 1.037, and 1.063, respectively. Fractionation factors for hydrogen were 1.203 (DMS) and 1.183 (TMA).
先前从河口沉积物中分离出的专性甲基营养球菌型产甲烷菌(GS-16 株)的特性描述如下。在二甲基硫(DMS)或三甲胺(TMA)上证明了生长,但在甲硫醇、甲硫醇加氢、二甲基二硫和蛋氨酸上则不行。当用含有这些化合物底物水平的培养基接种 DMS 培养的细胞时,它们能够同时代谢 DMS 和 TMA。然而,TMA 培养的细胞不能将 [C]DMS 代谢为 CH(4),尽管它们可以将 [C]甲醇代谢为 CH(4)。这些结果表明 DMS 的代谢途径与 TMA 和甲醇的代谢途径略有不同。在 25°C 下,在矿物培养基上分别以 TMA 和 DMS 生长时,该生物的倍增时间分别为 23 和 32 h。当在复杂肉汤中以 TMA 生长时,倍增时间更快(约 6 h)。在矿物培养基中,在 pH 值为 7.0 和 8.7 之间、29°C 时,以 0.2 至 0.4 M Na 和 0.04 M Mg 生长时,DMS 上的生长最快。在复杂肉汤中以 TMA 生长时,结果略有不同。细胞的 DNA 摩尔百分比 G+C 值为 44.5%。在 DMS、TMA 和甲醇上的生长产生了分别为 1.044、1.037 和 1.063 的稳定碳同位素分馏因子。氢的分馏因子分别为 1.203(DMS)和 1.183(TMA)。