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下调 和 在葡萄酒发酵过程中改变了酯类物质的组成。

Downregulation of and in Alters the Ester Profile of Wine during Fermentation.

机构信息

Shandong Provincial Key Laboratory of Microbial Engineering, School of Biologic Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250300, P.R. China.

State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250300, P.R. China.

出版信息

J Microbiol Biotechnol. 2022 Jun 28;32(6):761-767. doi: 10.4014/jmb.2201.01008. Epub 2022 Apr 10.

Abstract

and are the key genes involved in the synthesis of ethyl esters during wine fermentation. We constructed single (, ) and double () heterogenous mutant strains of the industrial diploid wine yeast EC1118 by disrupting one allele of and/or . In addition, the aromatic profile of wine produced during fermentation of simulated grape juice by these mutant strains was also analyzed. The expression levels of and/or in the relevant mutants were less than 50% of the wild-type strain when grown in YPD medium and simulated grape juice medium. Compared to the wild-type strain, all mutants produced lower amounts of ethyl esters in the fermented grape juice and also resulted in distinct ethyl ester profiles. , a gene involved in acetate ester synthesis, was expressed at higher levels in the downregulation mutants compared to the wild-type and strains during fermentation, which was consistent with the content of acetate esters. In addition, the production of higher alcohols was also markedly affected by the decrease in levels. Compared to , downregulation had a greater impact on the production of acetate esters and higher alcohols, suggesting that controlling expression could be an effective means to regulate the content of these aromatic metabolites in wine. Taken together, the synthesis of ethyl esters can be decreased by deleting one allele of and in the diploid EC1118 strain, which may modify the ester profile of wine more subtly compared to the complete deletion of target genes.

摘要

和 是葡萄酒发酵过程中乙基酯合成的关键基因。我们通过破坏工业二倍体葡萄酒酵母 EC1118 中一个等位基因的方法构建了单(,)和双()异源突变株。此外,还分析了这些突变株在模拟葡萄汁发酵过程中葡萄酒的香气特征。在 YPD 培养基和模拟葡萄汁培养基中生长时,相关突变株中 或 的表达水平低于野生型菌株的 50%。与野生型菌株相比,所有突变株在发酵葡萄汁中产生的乙基酯量较低,并且产生了不同的乙基酯谱。,一个参与乙酸酯合成的基因,在发酵过程中,与野生型和 菌株相比,在 下调突变株中的表达水平更高,这与乙酸酯的含量一致。此外,高级醇的产生也受到 水平降低的显著影响。与 相比,下调对乙酸酯和高级醇的产生影响更大,表明控制 表达可能是调节葡萄酒中这些芳香代谢物含量的有效手段。总之,通过删除二倍体 EC1118 菌株中 一个等位基因的方法可以降低乙基酯的合成,与完全删除目标基因相比,这可能使葡萄酒的酯谱更微妙地改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aceb/9628906/53248866c2bb/jmb-32-6-761-f1.jpg

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