Department of Microbiology and School of Oceanography, Oregon State University, Corvallis, Oregon 97331-3804, and Pacific Marine Environmental Laboratory, National Oceanic and Atmospheric Administration, Seattle, Washington 98115.
Appl Environ Microbiol. 1982 Aug;44(2):435-46. doi: 10.1128/aem.44.2.435-446.1982.
Measurements of methane oxidation rates were made in southeastern Bering Sea water samples with [C]methane. The rate at which CO(2) evolved from samples exposed to one methane concentration was defined as the relative methane oxidation rate. Rate determinations at three methane concentrations were used to estimate methane oxidation kinetics. The rate constant calculated from the kinetics and the observed methane concentration in the same water sample were used to calculate an in situ methane oxidation rate and the turnover time. First-order kinetics were observed in essentially all experiments in which methane oxidation kinetics were measured. Relative methane oxidation rates were greater in waters collected at inshore stations than at the offshore stations and were greater in bottom samples than in surface samples. In most water samples analyzed, there was essentially no radioactivity associated with the cells. The resulting respiration percentages were therefore very high with a mean of >98%. These data suggest that most of the methane was used by the microflora as an energy source and that very little of it was used in biosynthesis. The relative methane oxidation rates were not closely correlated with methane concentrations and did not appear to be linked to either oxygen or dissolved inorganic nitrogen concentrations. However, there was a significant correlation with relative microbial activity. Our data suggest that the methane oxidizers were associated with the general microbial heterotrophic community. Since these organisms did not appear to be using methane as a carbon source, it is unlikely that they have been isolated and identified as methane oxidizers in the past.
测量了东南白令海水样中[C]甲烷的甲烷氧化速率。将暴露于一种甲烷浓度的样品中 CO2 释放的速率定义为相对甲烷氧化速率。在三种甲烷浓度下进行的速率测定用于估计甲烷氧化动力学。从动力学和同一水样中观察到的甲烷浓度计算出的速率常数用于计算原位甲烷氧化速率和周转时间。在基本所有测量甲烷氧化动力学的实验中,均观察到一级动力学。与近海站位相比,在近岸站位采集的水样中的相对甲烷氧化速率更高,在底层样本中的相对甲烷氧化速率高于在表层样本中的相对甲烷氧化速率。在大多数分析的水样中,与细胞相关的放射性基本不存在。因此,呼吸百分比非常高,平均值>98%。这些数据表明,大部分甲烷被微生物菌群用作能源,很少用于生物合成。相对甲烷氧化速率与甲烷浓度没有密切关联,似乎与氧气或溶解无机氮浓度无关。然而,与相对微生物活性存在显著相关性。我们的数据表明,甲烷氧化菌与一般微生物异养群落有关。由于这些生物体似乎没有将甲烷用作碳源,因此过去不太可能将它们分离并鉴定为甲烷氧化菌。