油田微生物学:确定微生物影响腐蚀风险的分子技术案例研究

Douglas Grant Bennet
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引用次数: 1

摘要

本文的目的是解释在油田调查微生物学研究中获得的有益信息,其中使用了分子微生物学技术。这些技术的包含突出了本来会被遗漏和/或误解的信息。在本次调查中使用的分子微生物技术包括定量聚合酶链反应(qPCR)和下一代测序(NGS)。PCR技术的目的是从无法检测到的起始物质中特异性地增加目标(基因)。第一步是从样品中提取DNA,随后进行qPCR技术。在qPCR过程中,基因拷贝在热循环过程中产生,并积累荧光标记物,可用于量化目标基因。与PCR技术类似,从样品中提取DNA并扩增DNA。在NGS中,这些DNA片段在被扩增之前被分类到一个小DNA片段库中。在测序步骤中,通过与DNA文库比较,从发出的光信号中依次识别扩增的每个DNA片段。获得的结果显示了传统方法无法检测到的重要附加信息。除了对已知的总原核生物和硫酸盐还原原核生物种群进行更高、更真实的定量分析外,还可以通过NGS技术分析鉴定其他DNA群。研究结果提供了宝贵的信息,这些信息随后被用于实施成功的、有针对性的缓解战略,以降低MIC对资产的风险。
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Oilfield Microbiology: Case Study of Molecular Techniques for Determining the Risk of Microbiologically Influenced Corrosion MIC
The objective of this paper is to explain the beneficial information obtained during a microbiological study of an oilfield survey, where molecular microbiology techniques where utilised. The inclusion of these techniques highlighted information that would have otherwise been missed and/or misinterpreted. The molecular microbiology techniques deployed during this survey included Quantitative Polymerase Chain Reaction (qPCR) and Next Generation Sequencing (NGS). The aim of PCR technology is to specifically increase a target (gene) from an undetectable amount of starting material. The first step is extraction of DNA from the sample, which will subsequently be subjected to the qPCR technology. During qPCR gene copies are made during thermocycling and a fluorescent marker accumulates, which can be used to quantify the target gene. Similar to the PCR technology, DNA is extracted from the sample and the DNA is amplified. In NGS, this is then sorted into a library of small DNA segments before they are amplified. During the sequencing step each DNA fragment amplified is sequentially identified from light signals emitted by comparing with a DNA library. The results obtained indicated crucial additional information that was not detected by traditional methods. In addition to much higher, truer quantification of known populations of Total Prokaryotes and Sulphate Reducing Prokaryotes, identification of other groups of DNA was possible through the NGS technique analysis. The results provided valuable information, which has subsequently been used to apply successful, targeted mitigation strategies to reduce the risk of MIC to assets.
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