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Development of a PCR assay based on the 16S-23S rDNA internal transcribed spacer for identification of strictly anaerobic bacterium Zymophilus

机译:基于16S-23S rDNA内部转录间隔子的PCR检测方法的开发,用于鉴定严格厌氧细菌Zymophilus

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摘要

PCR-primers were designed for identification of strictly anaerobic bacteria of the genus Zymophilus based on genus-specific sequences of the 16S-23S rDNA internal transcribed spacer region. The specificity of the primers was tested against 37 brewery-related non-target microorganisms that could potentially occur in the same brewery specimens. None DNA was amplified from any of the non-Zymophilus strains tested including genera from the same family (Pectinatus, Megasphaera, Selenomonas), showing thus 100% specificity. PCR assay developed in this study allows an extension of the spectra of detected beer spoilage microorganisms in brewery laboratories. (C) 2015 Elsevier Ltd. All rights reserved.
机译:基于16S-23S rDNA内部转录间隔区的属特异性序列,设计PCR引物来鉴定严格的厌氧菌属。测试了针对37种与啤酒厂相关的非目标微生物的引物的特异性,这些微生物可能在同一啤酒厂标本中出现。从包括相同家族(Pectinatus,Megasphaera,Selenomonas)的属中测试的任何非Zymophilus菌株均未扩增DNA,因此显示出100%的特异性。在这项研究中开发的PCR分析方法可以扩展啤酒实验室中检测到的啤酒变质微生物的光谱。 (C)2015 Elsevier Ltd.保留所有权利。

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