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Denitrifying bacteria anaerobically oxidize methane in the absence of Archaea

机译:在没有古生菌的情况下,反硝化细菌厌氧氧化甲烷

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摘要

Recently, a microbial consortium was shown to couple the anaerobic oxidation of methane to denitrification, predominantly in the form of nitrite reduction to dinitrogen gas. This consortium was dominated by bacteria of an as yet uncharacterized division and archaea of the order Methanosarcinales. The present manuscript reports on the upscaling of the enrichment culture, and addresses the role of the archaea in methane oxidation. The key gene of methanotrophic and methanogenic archaea, mcrA, was sequenced. The associated cofactor F-430 was shown to have a mass of 905 Da, the same as for methanogens and different from the heavier form (951 Da) found in methanotrophic archaea. After prolonged enrichment (> 1 year), no inhibition of anaerobic methane oxidation was observed in the presence of 20 mM bromoethane sulfonate, a specific inhibitor of MCR. Optimization of the cultivation conditions led to higher rates of methane oxidation and to the decline of the archaeal population, as shown by fluorescence in situ hybridization and quantitative MALDI-TOF analysis of F-430. Mass balancing showed that methane oxidation was still coupled to nitrite reduction in the total absence of oxygen. Together, our results show that bacteria can couple the anaerobic oxidation of methane to denitrification without the involvement of Archaea.
机译:最近,显示了一个微生物联合体,将甲烷的厌氧氧化与反硝化耦合,主要是将亚硝酸盐还原成氮气。该财团以尚未鉴定的细菌和甲烷八叠球菌的古细菌为主导。本手稿报道了浓缩文化的升级,并探讨了古细菌在甲烷氧化中的作用。对甲烷营养和产甲烷古细菌的关键基因mcrA进行了测序。与之相关的辅助因子F-430的质量为905 Da,与产甲烷菌的质量相同,与甲烷营养古菌中发现的重形式(951 Da)不同。延长浓缩时间(> 1年)后,在20 mM溴乙烷磺酸盐(MCR的特异性抑制剂)存在下,未观察到厌氧甲烷氧化的抑制作用。如F-430的荧光原位杂交和定量MALDI-TOF分析所示,优化培养条件导致甲烷氧化速率加快,古细菌种群减少。质量平衡表明,在完全不存在氧气的情况下,甲烷氧化仍与亚硝酸盐还原有关。总之,我们的结果表明,细菌可以将甲烷的厌氧氧化与反硝化耦合,而无需古细菌的参与。

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