Department of Fermentation Science and Technology, Faculty of Applied Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo 156-8502, Japan.
Department of Biochemistry and Applied Bioscience, Faculty of Agriculture, University of Miyazaki, 1-1 Gakuenkibanadainishi, Miyazaki-shi, Miyazaki 889-2192, Japan.
J Biosci Bioeng. 2024 Mar;137(3):195-203. doi: 10.1016/j.jbiosc.2023.12.001. Epub 2024 Jan 19.
The EHL1/2/3 genes were identified by whole-genome sequencing of Kyokai No. 7 (K7), which is a well-known representative Japanese sake yeast Saccharomyces cerevisiae. The genes are present in K7, but not in laboratory strain S288C. Although the genes were presumed to encode epoxide hydrolase based on homology analysis, their effect on cellular metabolism in sake yeast has not yet been clarified. We constructed ehl1/2/3 mutants harboring a stop codon in each gene using the haploid yeast strain H3 as the parental strain, which was derived from K701, and investigated the physiological role and effects of the EHL1/2/3 genes on sake quality. Metabolome analysis and vitamin requirement testing revealed that the EHL1/2/3 genes are partly responsible for the synthesis of pantothenate. For fermentation profiles, ethanol production by the ehl1/2/3 mutant was comparable with that of strain H3, but succinate production was decreased in the ehl1/2/3 mutant compared to strain H3 when cultured in yeast malt (YM) medium containing 10% glucose and during sake brewing. Ethyl hexanoate and isoamyl acetate levels in the ehl1/2/3 mutant strain were decreased compared to those of strain H3 during sake brewing. Thus, the EHL1/2/3 genes did not affect ethanol production but did affect the production of organic acids and aromatic components during sake brewing.
EHL1/2/3 基因是通过对著名的日本清酒酵母 Saccharomyces cerevisiae 代表菌株 Kyokai No.7(K7)的全基因组测序鉴定的。这些基因存在于 K7 中,但不存在于实验室菌株 S288C 中。尽管这些基因根据同源性分析被推测编码环氧化物水解酶,但它们在清酒酵母中的细胞代谢作用尚未阐明。我们使用源自 K701 的单倍体酵母菌株 H3 作为亲本菌株,构建了每个基因都带有终止密码子的 ehl1/2/3 突变体,并研究了 EHL1/2/3 基因对清酒质量的生理作用和影响。代谢组学分析和维生素需求测试表明,EHL1/2/3 基因部分负责泛酸的合成。对于发酵特征,ehl1/2/3 突变体的乙醇产量与 H3 菌株相当,但与 H3 菌株相比,在含有 10%葡萄糖的酵母麦芽(YM)培养基中培养时,ehl1/2/3 突变体的琥珀酸产量降低,在清酒酿造过程中也是如此。与 H3 菌株相比,ehl1/2/3 突变株在清酒酿造过程中的乙基己酸和异戊酸乙酯水平降低。因此,EHL1/2/3 基因不影响乙醇产量,但影响清酒酿造过程中有机酸和芳香成分的产生。