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Construction of a Quadruple Auxotrophic Mutant of an Industrial Polyploid Saccharomyces cerevisiae Strain by Using RNA-Guided Cas9 Nuclease

机译:RNA指导Cas9核酸酶的工业多倍体酿酒酵母菌株的四倍营养缺陷型突变体的构建。

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摘要

Industrial polyploid yeast strains harbor numerous beneficial traits but suffer from a lack of available auxotrophic markers for genetic manipulation. Here we demonstrated a quick and efficient strategy to generate auxotrophic markers in industrial polyploid yeast strains with the RNA-guided Cas9 nuclease. We successfully constructed a quadruple auxotrophic mutant of a popular industrial polyploid yeast strain, Saccharomyces cerevisiae ATCC 4124, with ura3, trp1, leu2, and his3 auxotrophies through RNA-guided Cas9 nuclease. Even though multiple alleles of auxotrophic marker genes had to be disrupted simultaneously, we observed knockouts in up to 60% of the positive colonies after targeted gene disruption. In addition, growth-based spotting assays and fermentation experiments showed that the auxotrophic mutants inherited the beneficial traits of the parental strain, such as tolerance of major fermentation inhibitors and high temperature. Moreover, the auxotrophic mutants could be transformed with plasmids containing selection marker genes. These results indicate that precise gene disruptions based on the RNA-guided Cas9 nuclease now enable metabolic engineering of polyploid S. cerevisiae strains that have been widely used in the wine, beer, and fermentation industries.
机译:工业多倍体酵母菌株具有许多有益特性,但缺乏用于基因操作的可用营养缺陷型标记。在这里,我们展示了一种快速有效的策略,可利用RNA引导的Cas9核酸酶在工业多倍体酵母菌株中产生营养缺陷型标记。我们成功构建了一个受欢迎的工业多倍体酵母菌株酿酒酵母ATCC 4124的四倍营养缺陷型突变体,并通过RNA引导的Cas9核酸酶与ura3,trp1,leu2和his3营养缺陷型。即使必须同时破坏营养缺陷型标记基因的多个等位基因,我们也观察到靶向基因破坏后高达60%的阳性菌落的敲除。此外,基于生长的斑点检测和发酵实验表明,营养缺陷型突变体继承了亲本菌株的有益特性,例如主要发酵抑制剂的耐受性和高温。此外,营养缺陷型突变体可用含有选择标记基因的质粒转化。这些结果表明,基于RNA引导的Cas9核酸酶的精确基因破坏现在使多倍体酿酒酵母菌株的代谢工程化成为可能,该菌株已被广泛用于葡萄酒,啤酒和发酵行业。

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