首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Metatranscriptome of an Anaerobic Benzene-Degrading Nitrate-Reducing Enrichment Culture Reveals Involvement of Carboxylation in Benzene Ring Activation
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Metatranscriptome of an Anaerobic Benzene-Degrading Nitrate-Reducing Enrichment Culture Reveals Involvement of Carboxylation in Benzene Ring Activation

机译:厌氧苯降解减少硝酸盐的富集培养的转录组揭示了羧基化在苯环活化中的参与。

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摘要

The enzymes involved in the initial steps of anaerobic benzene catabolism are not known. To try to elucidate this critical step, a metatranscriptomic analysis was conducted to compare the genes transcribed during the metabolism of benzene and benzoate by an anaerobic benzene-degrading, nitrate-reducing enrichment culture. RNA was extracted from the mixed culture and sequenced without prior mRNA enrichment, allowing simultaneous examination of the active community composition and the differential gene expression between the two treatments. Ribosomal and mRNA sequences attributed to a member of the family Peptococcaceae from the order Clostridiales were essentially only detected in the benzene-amended culture samples, implicating this group in the initial catabolism of benzene. Genes similar to each of two subunits of a proposed benzene-carboxylating enzyme were transcribed when the culture was amended with benzene. Anaerobic benzoate degradation genes from strict anaerobes were transcribed only when the culture was amended with benzene. Genes for other benzoate catabolic enzymes and for nitrate respiration were transcribed in both samples, with those attributed to an Azoarcus species being most abundant. These findings indicate that the mineralization of benzene starts with its activation by a strict anaerobe belonging to the Peptococcaceae, involving a carboxylation step to form benzoate. These data confirm the previously hypothesized syntrophic association between a benzene-degrading Peptococcaceae strain and a benzoate-degrading denitrifying Azoarcus strain for the complete catabolism of benzene with nitrate as the terminal electron acceptor.
机译:涉及厌氧苯分解代谢初始步骤的酶尚不清楚。为了阐明这一关键步骤,进行了转录组分析,比较了厌氧苯降解,硝酸盐还原富集培养物中苯和苯甲酸酯代谢过程中转录的基因。从混合培养物中提取RNA并测序,无需事先进行mRNA富集,从而可以同时检查两种处理之间的活性群落组成和差异基因表达。基本上仅在苯修饰的培养样品中检测到来源于梭菌顺序的属于肽球菌科成员的核糖体和mRNA序列,这与苯的初始分解代谢有关。当用苯修正培养物时,转录出与拟议的苯羧化酶的两个亚基相似的基因。仅当用苯修正培养物时,才转录来自严格厌氧菌的厌氧苯甲酸酯降解基因。在这两个样品中都转录了其他苯甲酸酯分解代谢酶和硝酸盐呼吸的基因,其中那些归因于固氮菌种类最丰富。这些发现表明,苯的矿化作用是通过严格的属于拟球菌科的厌氧菌活化苯而开始的,涉及羧化步骤以形成苯甲酸盐。这些数据证实了先前假设的降解苯的肽球菌科菌株和降解苯甲酸酯的反硝化阿佐阿库斯菌株之间的同养关系,该降解过程是苯以硝酸盐为末端电子受体的完全分解代谢。

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