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Saccharomyces cerevisiae strains associated with the production of cacha?a: identification and characterization by traditional and molecular methods (PCR, PFGE and mtDNA-RFLP)

机译:与产酵母相关的酿酒酵母菌株:通过传统和分子方法(PCR,PFGE和mtDNA-RFLP)进行鉴定和表征

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摘要

A study of the genetic diversity of populations of Saccharomyces cerevisiae was conducted in ten different cacha?a producers (alambiques) in the southern state of Minas Gerais, Brazil. A total of 106 isolates were identified by PCR using the primer SCREC114, specific to S. cerevisiae, by pulsed-field gel electrophoresis (PFGE) and by restriction fragment polymorphism of mitochondrial DNA analysis (RFLP-mtDNA). PCR showed a product of amplification to 61 isolates, enabling a rapid identification of S. cerevisiae in different alambiques. Nine different profiles were found by PFGE; all the yeasts identified as S. cerevisiae by PCR had profiles similar to that of the marker S. cerevisiae, highlighting the specificity of primer SCREC114. RFLP-mtDNA, using four different enzymes, enabled the grouping of strains of S. cerevisiae, with 80%–100% similarity. Some alambiques that had a higher frequency of S. cerevisiae characterized by PCR and PFGE, had a lower level of genetic diversity determined by RFLP-mtDNA, indicating the ability of these strains to lead the fermentative process.
机译:在巴西南部的米纳斯吉拉斯州的十个不同的产茶者(阿拉伯人)中对酿酒酵母种群的遗传多样性进行了研究。使用引物SCREC114对啤酒酵母进行特异性鉴定,通过脉冲场凝胶电泳(PFGE)和线粒体DNA分析的限制性片段多态性(RFLP-mtDNA),通过PCR鉴定出总共106种分离物。 PCR显示扩增到61个分离株的产物,从而可以在不同的阿拉伯族群中快速鉴定酿酒酵母。 PFGE发现了九种不同的概况;通过PCR鉴定为酿酒酵母的所有酵母具有与标记酿酒酵母相似的谱,突出了引物SCREC114的特异性。 RFLP-mtDNA使用四种不同的酶,使酿酒酵母菌株分组,具有80%–100%的相似性。通过PCR和PFGE表征的酿酒酵母频率较高的某些类群,通过RFLP-mtDNA测定的遗传多样性水平较低,表明这些菌株具有领导发酵过程的能力。

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