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Application of Denaturing High-Performance Liquid Chromatography for Monitoring Sulfate-Reducing Bacteria in Oil Fields

机译:变性高效液相色谱法在油田硫酸盐还原菌监测中的应用

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Sulfate-reducing bacteria (SRB) participate in microbially induced corrosion (MIC) of equipment and H2S-driven reservoir souring in oil field sites. Successful management of industrial processes requires methods that allow robust monitoring of microbial communities. This study investigated the applicability of denaturing high-performance liquid chromatography (DHPLC) targeting the dissimilatory sulfite reductase ?-subunit (dsrB) gene for monitoring SRB communities in oil field samples from the North Sea, the United States, and Brazil. Fifteen of the 28 screened samples gave a positive result in real-time PCR assays, containing 9 × 101 to 6 × 105 dsrB gene copies ml?1. DHPLC and denaturing gradient gel electrophoresis (DGGE) community profiles of the PCR-positive samples shared an overall similarity; both methods revealed the same samples to have the lowest and highest diversity. The SRB communities were diverse, and different dsrB compositions were detected at different geographical locations. The identified dsrB gene sequences belonged to several phylogenetic groups, such as Desulfovibrio, Desulfococcus, Desulfomicrobium, Desulfobulbus, Desulfotignum, Desulfonatronovibrio, and Desulfonauticus. DHPLC showed an advantage over DGGE in that the community profiles were very reproducible from run to run, and the resolved gene fragments could be collected using an automated fraction collector and sequenced without a further purification step. DGGE, on the other hand, included casting of gradient gels, and several rounds of rerunning, excising, and reamplification of bands were needed for successful sequencing. In summary, DHPLC proved to be a suitable tool for routine monitoring of the diversity of SRB communities in oil field samples.
机译:硫酸盐还原细菌(SRB)参与了设备的微生物诱导腐蚀(MIC)和H2S驱动的油田现场油藏酸化。工业过程的成功管理需要能够对微生物群落进行强大监控的方法。这项研究调查了针对异化亚硫酸盐还原酶β亚基(dsrB)基因的变性高效液相色谱法(DHPLC)在监测北海,美国和巴西油田样品中的SRB群落中的适用性。在实时筛选的28个样本中,有15个在实时PCR分析中得到了阳性结果,其中包含9×101至6×105 dsrB基因拷贝ml?1。 PCR阳性样品的DHPLC和变性梯度凝胶电泳(DGGE)群落图具有总体相似性。两种方法均揭示出同一样本具有最低和最高的多样性。 SRB社区多种多样,并且在不同地理位置检测到不同的dsrB组成。鉴定出的dsrB基因序列属于几个系统发育组,例如脱硫弧菌,脱硫球菌,脱硫微生物,脱硫球菌,脱硫菌属,脱硫菌属和脱硫菌属。 DHPLC显示出优于DGGE的优势,因为每次运行之间的群落概况都非常可重现,并且可以使用自动馏分收集器收集分离的基因片段并进行测序,而无需进一步的纯化步骤。另一方面,DGGE包括梯度凝胶的浇铸,成功进行测序需要几轮重新运行,切除和重新扩增条带。总之,DHPLC被证明是常规监测油田样品中SRB群落多样性的合适工具。

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