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Rapid detection and identification of the metabolically diverse genus Gordonia by 16S rRNA-gene-targeted genus-specific primers

机译:通过16S rRNA基因靶向的属特异性引物快速检测和鉴定代谢多样性的属Gordonia

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摘要

The importance of the emerging genus Gordonia in industrial and environmental biotechnology is evidenced by the recent increase in associated publications and patents. But, investigations into potentially valuable Gordonia members are restricted by the limitations of current isolation and detection techniques. This motivated us to design a genus-specific oligonucleotide primer pair which could assist in rapid detection of species of the genus Gordonia by means of PCR-specific amplification. The Gordonia-specific 16S rDNA fragment (829 bp) was successfully amplified for all the reference Gordonia species with the designed primer pair G268F/G1096R. No amplification was noted for closely related species from other genera. The genus specificity was validated with 47 strains including wild-type isolates. Interestingly, two strains assigned earlier as Gordonia nitida (DSM 777) and Gordonia rubripertinctus (ATCC 21930) failed to produce a Gordonia-specific fragment with this primer pair. Further analysis of these two isolates based on 16S rDNA sequencing and phylogenetic analysis classified them to the genus Rhodococcus. Preliminary screening of soil samples with the Gordonia-specific primers was successful in terms of the rapid detection of nine Gordonia wild-type isolates. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:最近相关出版物和专利的增加证明了新兴的Gordonia属在工业和环境生物技术中的重要性。但是,对具有潜在价值的Gordonia成员的调查受到当前隔离和检测技术的限制。这促使我们设计一个属特异性寡核苷酸引物对,该引物对可通过PCR特异性扩增帮助快速检测Gordonia属物种。使用设计的引物对G268F / G1096R,成功扩增了所有参照Gordonia物种的Gordonia特异性16S rDNA片段(829 bp)。没有发现来自其他属的密切相关物种的扩增。用包括野生型分离物的47个菌株验证了属特异性。有趣的是,先前指定为nitord Gnitonia nitida(DSM 777)和Gordonia rubripertinctus(ATCC 21930)的两个菌株未能通过该引物对产生Gordonia特异性片段。根据16S rDNA测序对这两个分离株进行进一步分析,并在系统发育分析中将其分类为红球菌属。在快速检测9种Gordonia野生型分离株方面,用Gordonia特异性引物对土壤样品进行了初步筛选是成功的。 (c)2005年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

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