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Molecular Detection and Identification of Brettanomyces/Dekkera bruxellensis and Brettanomyces/Dekkera anomalus in Spoiled Wines

机译:变质酒中小菜蛾/德克酵母和异常小菜的分子检测与鉴定

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In this paper we describe the development of a PCR protocol to specifically detect Brettanomyces bruxellensis and B. anomalus. Primers DB90F and DB394R, targeting the D1-D2 loop of the 26S rRNA gene, were able to produce amplicons only when the DNA from these two species were used. No amplification product was obtained when DNA from other Brettanomyces spp. or wine yeasts were used as the templates. The 305-bp product was subjected to restriction enzyme analysis with DdeI to differentiate between B. bruxellensis and B. anomalus, and each species could be identified on the basis of the different restriction profiles. After optimization of the method by using strains from international collections, wine isolates were tested with the method proposed. Total agreement between traditional identification and molecular identification was observed. The protocol developed was also used for direct detection of B. bruxellensis and B. anomalus in wines suspected to be spoiled by Brettanomyces spp. Application of culture-based and molecular methods led us to the conclusion that 8 of 12 samples were spoiled by B. bruxellensis. Results based on the application of molecular methods suggested that two of the eight positive samples had been infected more recently, since specific signals were obtained at both the DNA and RNA levels.
机译:在本文中,我们描述了一种PCR协议的开发,该协议可特异性检测 Brettanomyces bruxellensis B。靶向26S rRNA基因D1-D2环的引物DB90F和DB394R仅在使用这两个物种的DNA时才能产生扩增子。其他 Brettanomyces spp的DNA没有扩增产物。或葡萄酒酵母用作模板。用 Dde I对305 bp的产物进行限制性酶切分析,以区分 B。布鲁塞尔 B。异常,并且可以根据不同的限制条件识别每个物种。在使用来自国际收藏品的菌株对方法进行优化之后,使用提出的方法对葡萄酒分离株进行了测试。观察到传统鉴定和分子鉴定之间完全一致。开发的协议还用于直接检测 B。布鲁塞尔 B。怀疑被 Brettanomyces spp变质的葡萄酒中的异常。应用基于文化的方法和分子方法得出的结论是12个样品中有8个被 B破坏了。布鲁塞尔。基于分子方法的结果表明,八种阳性样品中有两种是最近感染的,因为在DNA和RNA水平均获得了特异性信号。

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