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用聚合酶链式反应(PCR)检测水生样本中变形菌门β亚类的氨氧化细菌。

Detection of ammonium-oxidizing bacteria of the beta-subclass of the class Proteobacteria in aquatic samples with the PCR.

作者信息

Voytek M A, Ward B B

机构信息

Marine Sciences Program, University of California, Santa Cruz 95064, USA.

出版信息

Appl Environ Microbiol. 1995 Apr;61(4):1444-50. doi: 10.1128/aem.61.4.1444-1450.1995.

Abstract

The PCR was used as the basis for the development of a sensitive and specific assay for the detection of ammonium-oxidizing bacteria belonging to the beta-subclass of the class Proteobacteria. PCR primers were selected on the basis of nucleic acid sequence data available for seven species of nitrifiers in this subclass. The specificity of the ammonium oxidizer primers was evaluated by testing known strains of nitrifiers, several serotyped environmental nitrifier isolates, and other members of the Proteobacteria, including four very closely related, nonnitrifying species (as determined by rRNA sequence analysis). DNA extracts from 19 bacterio-plankton samples collected from Lake Bonney, Antarctica, and the Southern California Bight were assayed for the presence of ammonium oxidizers. By using a two-stage amplification procedure, ammonium oxidizers were detected in samples collected from both sites. Chemical data collected simultaneously support the occurrence of nitrification and the presence of nitrifiers. This is the first report describing PCR primers specific for ammonium-oxidizing bacteria and the successful amplification of nitrifier genes coding for rRNA from DNA extracts from natural samples. This application of PCR is of particular importance for the detection and study of microbes, such as autotrophic nitrifiers, which are difficult or impossible to isolate from indigenous microbial communities.

摘要

聚合酶链反应(PCR)被用作开发一种灵敏且特异的检测方法的基础,该方法用于检测属于变形菌纲β亚类的氨氧化细菌。PCR引物是根据该亚类中七种硝化细菌的核酸序列数据选择的。通过检测已知的硝化细菌菌株、几种血清型环境硝化细菌分离株以及变形菌纲的其他成员,包括四种密切相关的非硝化物种(通过rRNA序列分析确定),评估了氨氧化菌引物的特异性。对从南极邦尼湖和南加利福尼亚湾采集的19个浮游细菌样本的DNA提取物进行了氨氧化菌检测。通过使用两阶段扩增程序,在从两个地点采集的样本中检测到了氨氧化菌。同时收集的化学数据支持硝化作用的发生和硝化细菌的存在。这是第一份描述针对氨氧化细菌的特异性PCR引物以及从天然样本的DNA提取物中成功扩增编码rRNA的硝化细菌基因的报告。PCR的这种应用对于检测和研究诸如自养硝化细菌等难以或无法从本地微生物群落中分离的微生物尤为重要。

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