Tamura Hiroyasu, Okada Hiroki, Kume Kazunori, Koyano Takayuki, Goshima Tetsuya, Nakamura Ryo, Akao Takeshi, Shimoi Hitoshi, Mizunuma Masaki, Ohya Yoshikazu, Hirata Dai
a Research and Development Department , Asahi Sake Brewing Co., Ltd. , Nagaoka , Japan.
Biosci Biotechnol Biochem. 2015;79(7):1191-9. doi: 10.1080/09168451.2015.1020756. Epub 2015 Mar 19.
In the brewing of high-quality sake such as Daiginjo-shu, the cerulenin-resistant sake yeast strains with high producing ability to the flavor component ethyl caproate have been used widely. Genetic stability of sake yeast would be important for the maintenance of both fermentation properties of yeast and quality of sake. In eukaryotes, checkpoint mechanisms ensure genetic stability. However, the integrity of these mechanisms in sake yeast has not been examined yet. Here, we investigated the checkpoint integrity of sake yeasts, and the results suggested that a currently used cerulenin-resistant sake yeast had a defect in spindle assembly checkpoint (SAC). We also isolated a spontaneous cerulenin-resistant sake yeast FAS2-G1250S mutant, G9CR, which showed both high ethyl caproate-producing ability and integrity/intactness of the checkpoint mechanisms. Further, morphological phenotypic robustness analysis by use of CalMorph supported the genetic stability of G9CR. Finally, we confirmed the high quality of sake from G9CR in an industrial sake brewing setting.
在酿造诸如大吟酿等高品质清酒时,对风味成分己酸乙酯具有高产能力的抗浅蓝菌素清酒酵母菌株已被广泛使用。清酒酵母的遗传稳定性对于维持酵母的发酵特性和清酒品质都很重要。在真核生物中,检查点机制确保遗传稳定性。然而,清酒酵母中这些机制的完整性尚未得到研究。在此,我们研究了清酒酵母的检查点完整性,结果表明,目前使用的抗浅蓝菌素清酒酵母在纺锤体组装检查点(SAC)方面存在缺陷。我们还分离出了一种自发的抗浅蓝菌素清酒酵母FAS2 - G1250S突变体G9CR,它既具有高产己酸乙酯的能力,又具有检查点机制的完整性。此外,通过使用CalMorph进行的形态表型稳健性分析支持了G9CR的遗传稳定性。最后,我们在工业清酒酿造环境中证实了用G9CR酿造的清酒品质优良。