Marchesi J R, Sato T, Weightman A J, Martin T A, Fry J C, Hiom S J, Dymock D, Wade W G
School of Pure and Applied Biology, University of Wales College of Cardiff, United Kingdom.
Appl Environ Microbiol. 1998 Feb;64(2):795-9. doi: 10.1128/AEM.64.2.795-799.1998.
We report the design and evaluation of PCR primers 63f and 1387r for amplification of 16S rRNA genes from bacteria. Their specificity and efficacy were tested systematically with a bacterial species and environmental samples. They were found to be more useful for 16S rRNA gene amplification in ecological and systematic studies than PCR amplimers that are currently more generally used.
我们报告了用于从细菌中扩增16S rRNA基因的PCR引物63f和1387r的设计与评估。利用一种细菌物种和环境样本对它们的特异性和有效性进行了系统测试。结果发现,在生态学和系统学研究中,它们比目前更常用的PCR扩增引物在16S rRNA基因扩增方面更有用。