III号染色体非整倍体通过增加TUP1拷贝数增强工业酿酒酵母的乙醇耐受性

IF 5.2 2区 生物学
Sonia Albillos-Arenal, Javier Alonso del Real, Ana Cristina Adam, Eladio Barrio, Amparo Querol
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引用次数: 0

摘要

乙醇胁迫是酿酒酵母在发酵过程中面临的一个相当大的挑战。携带额外的III号染色体副本的菌株表现出增强的乙醇耐受性。在这里,我们研究了这种耐受性的潜在机制,重点是基因剂量效应和乙醇胁迫下的差异基因表达。我们比较了暴露于6%和10%乙醇中具有三拷贝III染色体的菌株及其两拷贝衍生株的基因表达谱。我们的分析发现,位于三号染色体上的TUP1是乙醇胁迫反应的关键调节因子。在耐受性菌株中删除1个拷贝的TUP1降低了其乙醇耐受性,这表明乙醇耐受性菌株的III号染色体非整倍性通过增加TUP1拷贝数来增强适应反应。我们的研究结果为乙醇耐受性的遗传基础提供了见解,具有优化工业发酵过程和理解非整倍体在工业酵母驯化中的作用的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chromosome III Aneuploidy Enhances Ethanol Tolerance in Industrial Saccharomyces cerevisiae by Increasing the TUP1 Copy Number

Chromosome III Aneuploidy Enhances Ethanol Tolerance in Industrial Saccharomyces cerevisiae by Increasing the TUP1 Copy Number

Ethanol stress poses a considerable challenge for Saccharomyces cerevisiae during fermentation. Strains carrying an extra copy of chromosome III exhibit enhanced ethanol tolerance. Here, we investigated the underlying mechanisms of this tolerance, focusing on gene dosage effects and differential gene expression under ethanol stress. We compared the gene expression profiles of a strain with three copies of chromosome III and its derivative with two copies, exposed to 6% and 10% ethanol. Our analysis identified TUP1, located on chromosome III, as a key regulator of the ethanol stress response. Deleting one copy of TUP1 in the tolerant strain diminished its ethanol tolerance, suggesting that chromosome III aneuploidy in ethanol-tolerant strains enhances adaptive responses by increasing TUP1 copy number. Our findings offer insights into the genetic basis of ethanol tolerance, with potential applications for optimising industrial fermentation processes and understanding the role of aneuploidy in the domestication of industrial yeasts.

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来源期刊
Microbial Biotechnology
Microbial Biotechnology Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
11.20
自引率
3.50%
发文量
162
审稿时长
1 months
期刊介绍: Microbial Biotechnology publishes papers of original research reporting significant advances in any aspect of microbial applications, including, but not limited to biotechnologies related to: Green chemistry; Primary metabolites; Food, beverages and supplements; Secondary metabolites and natural products; Pharmaceuticals; Diagnostics; Agriculture; Bioenergy; Biomining, including oil recovery and processing; Bioremediation; Biopolymers, biomaterials; Bionanotechnology; Biosurfactants and bioemulsifiers; Compatible solutes and bioprotectants; Biosensors, monitoring systems, quantitative microbial risk assessment; Technology development; Protein engineering; Functional genomics; Metabolic engineering; Metabolic design; Systems analysis, modelling; Process engineering; Biologically-based analytical methods; Microbially-based strategies in public health; Microbially-based strategies to influence global processes
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