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A Seamless Gene Deletion Method and Its Application for Regulation of Higher Alcohols and Ester in Baijiu Saccharomyces cerevisiae

机译:无缝基因删除方法及其在啤酒白酒中高级醇和酯调控中的应用

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摘要

The security of engineering Saccharomyces cerevisiae is becoming more focused on industrial production in consideration of the public concern regarding genetically modified organisms. In this work, a rapid and highly efficient system for seamless gene deletion in S. cerevisiae was developed through two-step integration protocol combined with endonuclease I-SCEI expression. The factors affecting the frequency of the second homologous recombination were optimized, and studies indicated that the mutant strains with 500 bp direct repeats and that have been incubating in galactose (0.5 g/100 mL) medium at 30°C and 180 r/min for 24 h permit high frequency (6.86 × 10−4) of the second homologous recombination. Furthermore, DNA sequence assays showed only self-DNA in native location without any foreign genes after deletion using this method. The seamless gene deletion method was applied to the construction of the engineering strains with BAT2 (encoding aminotransferase) deletion and ATF1 (alcohol acetyltransferases) overexpression. The mutants exhibited significant effects on higher alcohol reduction and ester improvement after Baijiu fermentation. The engineered strains can be used in industrial production in security, thereby meeting the requirements of modern science and technology.
机译:考虑到公众对转基因生物的关注,工程酿酒酵母的安全性正越来越集中于工业生产。在这项工作中,通过两步整合方案结合核酸内切酶I-SCEI表达,开发了一种快速高效的酿酒酵母无缝基因缺失系统。优化了影响第二次同源重组频率的因素,研究表明,具有500 bp直接重复的突变菌株已在半乳糖(0.5 g / 100 mL)培养基中于30°C和180 r / min孵育了30分钟, 24 h允许第二次同源重组的高频率(6.86×10 −4 )。此外,DNA序列分析显示,使用此方法删除后,仅在天然位置存在自身DNA,而没有任何外源基因。将无缝基因缺失方法应用于构建具有BAT2(编码氨基转移酶)缺失和ATF1(酒精乙酰基转移酶)过表达的工程菌株。该突变体对白酒发酵后的更高的醇还原率和酯的改善表现出显著作用。工程菌株可以安全地用于工业生产,从而满足现代科学技术的要求。

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