Laguerre G, Rigottier-Gois L, Lemanceau P
Laboratoire de Microbiologie des Sols, INRA, Dijon, France.
Mol Ecol. 1994 Oct;3(5):479-87. doi: 10.1111/j.1365-294x.1994.tb00126.x.
A rapid procedure for the identification of fluorescent pseudomonads, based on the polymerase chain reaction (PCR) and restriction fragment analysis of 16S rDNA genes is described. Thirty-one strains belonging to 10 different Pseudomonas species of the Pseudomonas fluorescens rRNA branch were characterized. Amplified rDNA was digested with 13 different restriction endonucleases. The combined data from restriction analysis enabled the definition of 17 different 16S rDNA genotypes. All type strains belonging to different species were differentiated. The good correlation between grouping obtained using restriction analysis with other molecular classification criteria demonstrates the value of the described method to characterize rapidly fluorescent Pseudomonas strains at the species level.
本文描述了一种基于聚合酶链反应(PCR)和16S rDNA基因限制性片段分析的快速鉴定荧光假单胞菌的方法。对荧光假单胞菌rRNA分支中10个不同假单胞菌属物种的31株菌株进行了特征分析。扩增的rDNA用13种不同的限制性内切酶进行消化。限制性分析的综合数据确定了17种不同的16S rDNA基因型。所有不同物种的模式菌株都得以区分。使用限制性分析获得的分组与其他分子分类标准之间的良好相关性证明了所描述方法在物种水平快速鉴定荧光假单胞菌菌株方面的价值。