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烃类污染环境和富集培养物中苄基琥珀酸合酶和烷基琥珀酸合酶基因的多样性。

Diversity of benzyl- and alkylsuccinate synthase genes in hydrocarbon-impacted environments and enrichment cultures.

机构信息

Department of Botany and Microbiology and Institute for Energy and the Environment, University of Oklahoma, Norman, Oklahoma 73019, USA.

出版信息

Environ Sci Technol. 2010 Oct 1;44(19):7287-94. doi: 10.1021/es1002023.

Abstract

Hydrocarbon-degrading microorganisms play an important role in the natural attenuation of spilled petroleum in a variety of anoxic environments. The role of benzylsuccinate synthase (BSS) in aromatic hydrocarbon degradation and its use as a biomarker for field investigations are well documented. The recent discovery of alkylsuccinate synthase (ASS) allows the opportunity to test whether its encoding gene, assA, can serve as a comparable biomarker of anaerobic alkane degradation. Degenerate assA- and bssA-targeted PCR primers were designed in order to survey the diversity of genes associated with aromatic and aliphatic hydrocarbon biodegradation in petroleum-impacted environments and enrichment cultures. DNA was extracted from an anaerobic alkane-degrading isolate (Desulfoglaeba alkenexedens ALDC), hydrocarbon-contaminated river and aquifer sediments, a paraffin-degrading enrichment, and a propane-utilizing mixed culture. Partial assA and bssA genes were PCR amplified, cloned, and sequenced, yielding several novel clades of assA genes. These data expand the range of alkane-degrading conditions for which relevant gene sequences are available and indicate that considerable diversity of assA genes can be found in hydrocarbon-impacted environments. The detection of genes associated with anaerobic alkane degradation in conjunction with the in situ detection of alkylsuccinate metabolites was also demonstrated. Comparable molecular signals of assA/bssA were not found when environmental metagenome databases of uncontaminated sites were searched. These data confirm that the assA gene is a useful biomarker for anaerobic alkane metabolism.

摘要

在各种缺氧环境中,烃类降解微生物在溢油的自然衰减中起着重要作用。苯丁烯二酸合酶(BSS)在芳烃降解中的作用及其作为现场调查生物标志物的用途已有充分的文献记载。最近发现的烷丁烯二酸合酶(ASS)为测试其编码基因 assA 是否可以作为厌氧烷烃降解的可比生物标志物提供了机会。设计了针对 assA 和 bssA 的简并 PCR 引物,以便调查与受石油影响的环境和富集培养物中的芳烃和脂肪烃生物降解相关的基因多样性。从厌氧烷烃降解分离物(Desulfoglaeba alkenexedens ALDC)、烃污染的河流和含水层沉积物、石蜡降解富集物和丙烷利用混合培养物中提取了 DNA。对部分 assA 和 bssA 基因进行了 PCR 扩增、克隆和测序,得到了几个新的 assA 基因分支。这些数据扩大了可获得相关基因序列的烷烃降解条件范围,并表明在烃污染环境中可以发现相当多的 assA 基因多样性。还证明了在原位检测烷基琥珀酸代谢物的同时检测与厌氧烷烃降解相关的基因。在搜索未污染地点的环境宏基因组数据库时,没有发现与 assA/bssA 相关的分子信号。这些数据证实了 assA 基因是厌氧烷烃代谢的有用生物标志物。

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