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土壤甲烷氧化菌对大气甲烷的氧化与同化。

Oxidation and assimilation of atmospheric methane by soil methane oxidizers.

出版信息

Appl Environ Microbiol. 1997 Mar;63(3):874-80. doi: 10.1128/aem.63.3.874-880.1997.

Abstract

The metabolism of atmospheric methane in a forest soil was studied by radiotracer techniques. Maximum (sup14)CH(inf4) oxidation (163.5 pmol of C cm(sup-3) h(sup-1)) and (sup14)C assimilation (50.3 pmol of C cm(sup-3) h(sup-1)) occurred at the A(inf2) horizon located 15 to 18 cm below the soil surface. At this depth, 31 to 43% of the atmospheric methane oxidized was assimilated into microbial biomass; the remaining methane was recovered as (sup14)CO(inf2). Methane-derived carbon was incorporated into all major cell macromolecules by the soil microorganisms (50% as proteins, 19% as nucleic acids and polysaccharides, and 5% as lipids). The percentage of methane assimilated (carbon conversion efficiency) remained constant at temperatures between 5 and 20(deg)C, followed by a decrease at 30(deg)C. The carbon conversion efficiency did not increase at methane concentrations between 1.7 and 1,000 ppm. In contrast, the overall methane oxidation activity increased at elevated methane concentrations, with an apparent K(infm) of 21 ppm (31 nM CH(inf4)) and a V(infmax) of 188 pmol of CH(inf4) cm(sup-3) h(sup-1). Methane oxidizers from soil depths with maximum methanotrophic activity respired approximately 1 to 3% of the assimilated methane-derived carbon per day. This apparent endogenous respiration did not change significantly in the absence of methane. Similarly, the potential for oxidation of atmospheric methane was relatively insensitive to methane starvation. Soil samples from depths above and below the zone with maximum atmospheric methane oxidation activity showed a dramatic increase in the turnover of the methane assimilated (>20 times increase). Physical disturbance such as sieving or mixing of soil samples decreased methane oxidation and assimilation by 50 to 58% but did not alter the carbon conversion efficiency. Ammonia addition (0.1 or 1.0 (mu)mol g fresh weight) decreased both methane oxidation and carbon conversion efficiency. This resulted in a dramatic decrease in methane assimilation (85 to 99%). In addition, ammonia-treated soil showed up to 10 times greater turnover of the assimilated methane-derived carbon (relative to untreated soil). The results suggest a potential for microbial growth on atmospheric methane. However, growth was regulated strongly by soil parameters other than the methane concentration. The pattern observed for metabolism of atmospheric methane in soils was not consistent with the physiology of known methanotrophic bacteria.

摘要

利用放射性示踪技术研究了森林土壤中大气甲烷的代谢。最大(上 14)CH(下 4)氧化(163.5 pmol 的 C cm(上-3)h(上-1))和(上 14)C 同化(50.3 pmol 的 C cm(上-3)h(上-1))发生在距土壤表面 15 至 18 厘米的 A(下 2)层。在这个深度,31%至 43%的大气甲烷被氧化为微生物生物量;其余的甲烷作为(上 14)CO(下 2)被回收。土壤微生物将甲烷衍生的碳纳入所有主要细胞大分子(50%为蛋白质,19%为核酸和多糖,5%为脂质)。在 5 至 20°C 之间,甲烷同化的百分比(碳转化效率)保持不变,然后在 30°C 时下降。在 1.7 至 1000 ppm 之间的甲烷浓度下,甲烷同化的碳转化率并没有增加。相比之下,在升高的甲烷浓度下,整体甲烷氧化活性增加,表观 Km 为 21 ppm(31 nM CH(下 4)),Vmax 为 188 pmol 的 CH(下 4)cm(上-3)h(上-1)。具有最大甲烷氧化活性的土壤深度的甲烷氧化菌每天呼吸约 1%至 3%同化的甲烷衍生碳。在没有甲烷的情况下,这种明显的内源性呼吸没有显著变化。同样,大气甲烷氧化的潜力对甲烷饥饿相对不敏感。在最大大气甲烷氧化活性区域以上和以下的土壤样本中,甲烷同化的周转率(增加 20 倍以上)显著增加。土壤样本的物理干扰,如筛选或混合,使甲烷氧化和同化减少 50%至 58%,但不会改变碳转化率。添加氨(0.1 或 1.0(mu)mol g [鲜重](上-1))会降低甲烷氧化和碳转化率。这导致甲烷同化的急剧下降(85%至 99%)。此外,氨处理的土壤显示出高达 10 倍的同化甲烷衍生碳的周转率(相对于未处理的土壤)。结果表明微生物有可能以大气甲烷为生长基质。然而,生长受除甲烷浓度以外的土壤参数强烈调节。在土壤中观察到的大气甲烷代谢模式与已知的甲烷氧化细菌的生理学不一致。

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