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PCR-TTGE and RAPD-PCR Techniques to Analyze Saccharomyces cerevisiae and Saccharomyces carlsbergensis Isolated from Craft Beers

机译:PCR-TTGE和RAPD-PCR技术分析精酿啤酒中的啤酒酵母和嘉士伯酵母

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摘要

In the Friuli Venezia Giulia region (North East of Italy) the production of craft beers has been increasing constantly. Usually microbreweries use yeasts supplied by Italian or foreign industrial breweries for beer production. Yeast species are often not known, moreover the vitality, the viability, the physiological state and the number of generation are not known. To improve the quality of the final product it is important to evaluate the quality of the yeast strain used and the lactic acid bacteria contamination. Various molecular methods have been developed to compare genetic characteristics of yeast strains used in beer and wine production. The methods proposed in this work, PCR-TTGE and RAPD-PCR techniques, allow the comparison of specific DNA sequences to identify and/or characterize yeast strains. The molecular methods are faster than traditional methods and they allowed the identification of the strains analysed as S. cerevisiae and the intraspecies differentiation among yeast strains tested within 8 h after cell growth.
机译:在弗留利威尼斯朱利亚地区(意大利东北部),精酿啤酒的产量一直在增长。通常,微型啤酒厂使用意大利或外国工业啤酒厂提供的酵母来生产啤酒。酵母菌种通常是未知的,而且其活力,生存力,生理状态和世代数也不清楚。为了提高最终产品的质量,重要的是评估所用酵母菌株的质量和乳酸菌的污染。已经开发了各种分子方法来比较啤酒和葡萄酒生产中使用的酵母菌株的遗传特性。在这项工作中提出的方法,PCR-TTGE和RAPD-PCR技术,允许比较特定的DNA序列以鉴定和/或表征酵母菌株。分子方法比传统方法更快,它们可以鉴定分析为酿酒酵母的菌株,并可以在细胞生长后8小时内测试酵母菌株之间的种内分化。

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