Mehling A, Wehmeier U F, Piepersberg W
Bergische Universität GH Wuppertal, AG Chemische Mikrobiologie, Wuppertal, Federal Republic of Germany.
Microbiology (Reading). 1995 Sep;141 ( Pt 9):2139-47. doi: 10.1099/13500872-141-9-2139.
To facilitate the differential identification of the genus Streptomyces, the 16S rRNA genes of 17 actinomycetes were sequenced and screened for the existence of streptomycete-specific signatures. The 16S rDNA of the Streptomyces strains and Amycolatopsis orientalis subsp. lurida exhibited 95-100% similarity, while that of the 16S rDNA of Actinoplanes utahensis showed only 88% similarity to the streptomycete 16S rDNAs. Potential genus-specific sequences were found in regions located around nucleotide positions 120, 800 and 1100. Several sets of primers derived from these characteristic regions were investigated as to their specificity in PCR-mediated amplifications. Most sets allowed selective amplification of the streptomycete rDNA sequences studied. RFLPs in the 16S rDNA permitted all strains to be distinguished.
为便于对链霉菌属进行鉴别,对17株放线菌的16S rRNA基因进行测序,并筛选链霉菌特异性特征的存在情况。链霉菌菌株和东方拟无枝酸菌亚种鲁氏亚种的16S rDNA显示出95%-100%的相似性,而犹他游动放线菌的16S rDNA与链霉菌16S rDNA仅显示88%的相似性。在核苷酸位置120、800和1100附近的区域发现了潜在的属特异性序列。研究了从这些特征区域衍生的几套引物在PCR介导扩增中的特异性。大多数引物组允许对所研究的链霉菌rDNA序列进行选择性扩增。16S rDNA中的限制性片段长度多态性(RFLPs)可区分所有菌株。