von Wintzingerode F, Göbel U B, Stackebrandt E
Institut für Mikrobiologie und Hygiene, Universitätsklinikum Charité, Berlin, Germany.
FEMS Microbiol Rev. 1997 Nov;21(3):213-29. doi: 10.1111/j.1574-6976.1997.tb00351.x.
After nearly 10 years of PCR-based analysis of prokaryotic small-subunit ribosomal RNAs for ecological studies it seems necessary to summarize reported pitfalls of this approach which will most likely lead to an erroneous description on the microbial diversity of a given habitat. The following article will cover specific aspects of sample collection, cell lysis, nucleic acid extraction, PCR amplification, separation of amplified DNA, application of nucleic probes and data analysis.
在基于聚合酶链式反应(PCR)对原核生物小亚基核糖体RNA进行了近10年的生态学研究分析之后,似乎有必要总结一下该方法中已报道的缺陷,这些缺陷很可能导致对特定栖息地微生物多样性的错误描述。以下文章将涵盖样本采集、细胞裂解、核酸提取、PCR扩增、扩增DNA的分离、核酸探针的应用以及数据分析等具体方面。