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含有新型FAS2突变的自克隆酵母菌株在日本清酒中产生更高量的己酸乙酯。

Self-cloning yeast strains containing novel FAS2 mutations produce a higher amount of ethyl caproate in Japanese sake.

作者信息

Aritomi Kazuo, Hirosawa Isao, Hoshida Hisashi, Shiigi Mikio, Nishizawa Yoshinori, Kashiwagi Susumu, Akada Rinji

机构信息

Yamaguchi Prefectural Industrial Technology Institute, Ube, Japan.

出版信息

Biosci Biotechnol Biochem. 2004 Jan;68(1):206-14. doi: 10.1271/bbb.68.206.

Abstract

Point mutation of Gly1250Ser (1250S) of the yeast fatty acid synthase gene FAS2 confers cerulenin resistance. This mutation also results in a higher production of the apple-like flavor component ethyl caproate in Japanese sake. We mutated the 1250th codon by in vitro site-directed mutagenesis to encode Ala (1250A) or Cys (1250C) and examined cerulenin resistance and ethyl caproate production. The mutated FAS2 genes were inserted into a binary plasmid vector containing a drug-resistance marker and a counter-selectable marker, GALp-GIN11M86. The plasmids were integrated into the wild-type FAS2 locus of a sake yeast strain, and the loss of the plasmid sequences from the integrants was done by growth on galactose plates, which is permissive for loss of GALp-GIN11M86. These counter-selected strains contained either the wild type or the mutated FAS2 allele but not the plasmid sequences, from which FAS2 mutant strains were selected by allele-specific PCR. The FAS2-1250C mutant produced a higher amount of ethyl caproate in sake than FAS2-1250S, while FAS2-1250A produced an ethyl caproate level intermediate between FAS2-1250S and the parental Kyokai no. 7 strain. Interestingly, these mutants only showed detectable cerulenin resistance. These 'self-cloning' yeast strains should be acceptable to the public because they can improve sake quality without the presence of extraneous DNA sequences.

摘要

酵母脂肪酸合酶基因FAS2的Gly1250Ser(1250S)点突变赋予了对浅蓝菌素的抗性。该突变还导致日本清酒中苹果风味成分己酸乙酯的产量更高。我们通过体外定点诱变对第1250个密码子进行突变,以编码丙氨酸(1250A)或半胱氨酸(1250C),并检测了对浅蓝菌素的抗性和己酸乙酯的产量。将突变的FAS2基因插入含有耐药标记和反选择标记GALp - GIN11M86的二元质粒载体中。将质粒整合到清酒酵母菌株的野生型FAS2基因座中,通过在允许GALp - GIN11M86缺失的半乳糖平板上生长,使整合体中的质粒序列丢失。这些反选择的菌株含有野生型或突变的FAS2等位基因,但不含有质粒序列,通过等位基因特异性PCR从中筛选出FAS2突变菌株。FAS2 - 1250C突变体在清酒中产生的己酸乙酯量比FAS2 - 1250S高,而FAS2 - 1250A产生的己酸乙酯水平介于FAS2 - 1250S和亲本七号酵母菌株之间。有趣的是,这些突变体仅表现出可检测到的对浅蓝菌素的抗性。这些“自我克隆”酵母菌株应该会被公众接受,因为它们可以在不存在外来DNA序列的情况下提高清酒质量。

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