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首页> 外文期刊>FEMS Microbiology Ecology >Diversity and geographical distribution of members of the Streptomyces violaceusniger 16S rRNA gene clade detected by clade-specific PCR primers
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Diversity and geographical distribution of members of the Streptomyces violaceusniger 16S rRNA gene clade detected by clade-specific PCR primers

机译:进化枝特异性PCR引物检测紫链霉菌16S rRNA基因进化枝成员的多样性和地理分布

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摘要

The Streptomyces violaceusniger 16S rRNA gene clade contains organisms that are of ecological interest and a rich source of novel bioactive metabolites. Improvements in the classification of members of the S. violaceusniger clade made it possible to design, evaluate and use an oligonucleotide primer set to gain an insight into the presence, distribution and taxonomic diversity of members of this taxon in environmental samples. In silico testing showed that the primers had a perfect match with representatives of the S. violaceusniger clade. The primers, designated S-S-Svio-66-a-S-20 and S-S-Svio-1274-a-A-20, amplified an approximate to 1190-bp stretch of 16S rRNA gene from authenticated members of the S. violaceusniger clade, but not from representatives of other actinomycete taxa. Following amplification of DNA extracted from sediment and soil samples, the sequences of cloned PCR products confirmed the specific amplification of target sequences in 87% of the clones; the use of 16S rRNA gene fragment similarity correlations indicated that the clones represented new species. The primers can be used to facilitate the isolation of novel members of the S. violaceusniger 16S rRNA gene clade by allowing prescreening of environmental samples and the subsequent detection and retrieval of targetted strains through the use of selective isolation procedures.
机译:Violaceusniger链霉菌16S rRNA基因进化枝包含具有生态学意义的生物和丰富的新型生物活性代谢物来源。紫罗兰链球菌进化枝成员的分类的改进使得设计,评估和使用寡核苷酸引物组成为可能,以了解环境样品中该分类群成员的存在,分布和分类学多样性。在计算机测试中,该引物与紫罗兰S. violaceusniger进化枝的代表完美匹配。命名为SS-Svio-66-aS-20和SS-Svio-1274-aA-20的引物从经鉴定的S. violaceusniger进化枝成员扩增了约1190 bp的16S rRNA基因片段,但未从代表中扩增出其他放线菌类群。从沉积物和土壤样品中提取的DNA扩增后,克隆的PCR产物的序列证实了87%的克隆中靶序列的特异性扩增。 16S rRNA基因片段相似性相关性的使用表明该克隆代表了新物种。通过允许对环境样品进行预筛选以及随后通过使用选择性分离程序对目标菌株进行检测和检索,可以使用引物来促进紫红色葡萄球菌16S rRNA基因进化枝的新成员的分离。

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