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Isolation of a spontaneous cerulenin-resistant sake yeast with both high ethyl caproate-producing ability and normal checkpoint integrity

机译:具有高己酸乙酯生产能力和正常检查点完整性的自发抗蓝绿色素清酒酵母的分离

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摘要

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.
机译:在诸如大吟酿树之类的优质清酒的酿造中,对风味成分己酸乙酯具有高生产能力的耐蓝霉素的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质量都至关重要。在真核生物中,检查点机制可确保遗传稳定性。然而,尚未检测到清酒酵母中这些机制的完整性。在这里,我们调查了清酒酵母检查点的完整性,结果表明,目前使用的耐蓝霉素的清酒酵母在纺锤体装配检查点(SAC)中存在缺陷。我们还分离了自发的抗蓝绿色素清酒酵母FAS2-G1250S突变体G9CR,该突变体既显示出高己酸乙酯生成能力,又显示了检查点机制的完整性/完整性。此外,通过使用CalMorph的形态表型鲁棒性分析支持了G9CR的遗传稳定性。最后,我们确认了G9CR在工业清酒酿造环境中的高品质清酒。

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  • 来源
    《酒類総合研究所報告》 |2016年第188期|60-60|共1页
  • 作者单位

    Research and Development Department, Asahi Sake Brewing Co., Ltd., Nagaoka, Japan ,Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima, Japan;

    Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa,Japan;

    Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima, Japan;

    Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima, Japan;

    National Research Institute of Brewing, Higashi-Hiroshima, Japan;

    Research and Development Department, Asahi Sake Brewing Co., Ltd., Nagaoka, Japan;

    National Research Institute of Brewing, Higashi-Hiroshima, Japan;

    Department of Biological Chemistry and Food Sciences, Iwate University, Morioka, Japan;

    Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima, Japan;

    Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa,Japan;

    Research and Development Department, Asahi Sake Brewing Co., Ltd., Nagaoka, Japan ,Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima, Japan;

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