首页> 外文会议>Proceedings of 2011 international symposium - multi-field coupling theory of rock and soil and its applications in exploitation and utilization of resources >Microbial Diversity Analysis of Reservoirs After Polymer Flooding in Daqing Oil Field at the Middle Stage of Microbial Profile Modification
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Microbial Diversity Analysis of Reservoirs After Polymer Flooding in Daqing Oil Field at the Middle Stage of Microbial Profile Modification

机译:大庆油田聚合物剖面改造中期聚合物驱后储层微生物多样性分析

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摘要

To gain a better understanding of the mechanism and technology of microbial enhanced oil recovery, microbial community structure and diversity of reservoirs after polymer flooding in Daqing oil field at the Middle Stage of microbial profile modification were studied. Research methodology: DNA was extracted from four oil well samples after polymer flooding in the Daqing Oilfield, Heilongjiang, China. A 16S rDNA clone library was constructed by PCR amplification with universal primers. Research result: 101 clones were obtained and classified into 9 different operational taxonomic units (OTUs). Four OTUs had more than five clones occupied most of the 16S rDNA clone library, while 5 OTUs had only one clone. At the same time, the microbial diversity of the 16S rDNA clone library was evaluated by coverage value (C), Shannon-Weiner index (H) and Margalef index (M). Phylogenetic analysis revealed that the dominant microbes of the library belonged to uncultured bacteria (55%). Cultured bacteria are composed of Alphaproteobacteria (3%), Gammaproteobacteria (35%), Deltaproteobacteria (4%) and Epsilonproteobacteria (1%). The Pseudomonas related with hydrocarbon biodegradation and surfactant production accounted for 25 % in the clone library.
机译:为了更好地了解微生物提高采收率的机理和技术,研究了大庆油田聚合物剖面改造中期聚合物驱后的微生物群落结构和储层多样性。研究方法:在黑龙江大庆油田进行聚合物驱后,从四个油井样品中提取DNA。通过通用引物的PCR扩增,构建了16S rDNA克隆文库。研究结果:获得101个克隆并将其分类为9个不同的操作分类单位(OTU)。四个OTU具有超过五个克隆,占据了16S rDNA克隆库的大部分,而五个OTU只有一个克隆。同时,通过覆盖率值(C),香农-韦纳指数(H)和玛格丽夫指数(M)评价16S rDNA克隆文库的微生物多样性。系统发育分析表明,该文库的优势微生物属于未培养细菌(55%)。培养的细菌由α-变形杆菌(3%),γ-变形杆菌(35%),Delta变形杆菌(4%)和Epsilon变形细菌(1%)组成。在克隆文库中,与烃生物降解和表面活性剂产生有关的假单胞菌占25%。

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