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Saccharomyces cerevisiae FLO1 Gene Demonstrates Genetic Linkage to Increased Fermentation Rate at Low Temperatures

机译:酿酒酵母FLO1基因表明遗传联系增加了低温下的发酵速率。

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摘要

Low fermentation temperatures are of importance to food and beverage industries working with Saccharomyces cerevisiae. Therefore, the identification of genes demonstrating a positive impact on fermentation kinetics is of significant interest. A set of 121 mapped F1 progeny, derived from a cross between haploid strains BY4716 (a derivative of the laboratory yeast S288C) and wine yeast RM11-1a, were fermented in New Zealand Sauvignon Blanc grape juice at 12.5°. Analyses of five key fermentation kinetic parameters among the F1 progeny identified a quantitative trait locus (QTL) on chromosome I with a significant degree of linkage to maximal fermentation rate (Vmax) at low temperature. Independent deletions of two candidate genes within the region, and , were constructed in the parental strains (with S288C representing BY4716). Fermentation of wild-type and deletion strains at 12.5 and 25° confirmed that the genetic linkage to Vmax corresponds to the S288C version of the allele, as the absence of this allele reduced Vmax by ∼50% at 12.5°, but not at 25°. Reciprocal hemizygosity analysis (RHA) between S288C and RM11-1a alleles did not confirm the prediction that the S288C version of was promoting more rapid fermentation in the opposing strain background, suggesting that the positive effect on Vmax derived from S288C may only provide an advantage in haploids, or is dependent on strain-specific cis or trans effects. This research adds to the growing body of evidence demonstrating the role of in providing stress tolerance to S. cerevisiae during fermentation.
机译:较低的发酵温度对使用酿酒酵母的食品和饮料行业至关重要。因此,鉴定对发酵动力学有积极影响的基因是非常重要的。一组来自单倍体菌株BY4716(实验室酵母S288C的衍生物)和葡萄酒酵母RM11-1a杂交的121个定位的F1后代在12.5°的新西兰长相思葡萄汁中发酵。对F1子代中五个关键发酵动力学参数的分析确定了I号染色体上的数量性状基因座(QTL),该数量性状基因座与低温下的最大发酵速率(Vmax)有显着的关联。在亲本菌株中构建了该区域内的两个候选基因和的独立缺失(S288C代表BY4716)。在12.5和25°发酵野生型和缺失菌株证实,与Vmax的遗传连锁对应于等位基因的S288C版本,因为缺少该等位基因会在12.5°降低Vmax约50%,但在25°不会降低。 S288C和RM11-1a等位基因之间的相互半合子分析(RHA)未能证实以下预测:S288C版本在相反的菌株背景下促进了更快的发酵,这表明对S288C衍生的Vmax的积极作用可能仅提供了优势。单倍体,或取决于菌株特异性的顺式或反式作用。这项研究增加了越来越多的证据,证明了在发酵过程中对酿酒酵母提供抗逆性的作用。

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