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本研究以酿酒酵母AS2.1189为亲株,利用亚硝酸诱变酵母并建立含561株诱变株的菌种库,通过耐性平板点种初筛法,经5次传代培养后筛选得到遗传性能稳定的耐性诱变株,其中Y75、Y226、Y324这3株是耐热、耐渗透压和耐酒精性能都有提高的诱变株。3株诱变株在亲株极限耐受条件下的生长速率和最终细胞浓度都要大于亲株。研究诱变株Y75在胁迫条件下利用蔗汁发酵酒精,结果表明Y75最高菌体浓度高出亲株约2.5个OD600单位;Y75发酵液pH低于亲株约0.4个单位;Y75耗糖速率明显大于亲株,但最终残糖基本相同;发酵20 h后Y75的产酒度高于亲株约1%(体积分数,下同),Y75和亲株的最终产酒度为14.82%和14.22%。 相似文献
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酒精发酵过程中酿酒酵母海藻糖代谢的研究 总被引:15,自引:0,他引:15
研究了酿酒酵母在酒精发酵过程中酵母细胞内海藻糖的代谢。结果表明海藻糖的代谢受几种因素如底物浓度、发酵温度以及其他条件的调节与控制。在试验中对酿酒酵母细胞内海藻糖在整个酒精发酵过程中的生物功能作了简要的评价。 相似文献
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利用紫外辐照的方式对从葡萄表面筛选的菌株Y6进行诱变,选育出产酒精能力强、产酸能力高并且发酵性能稳定的酿酒酵母菌株。通过单因素试验选择酵母菌株距30 W紫外灯30 cm照射100 s,致死率为75.62%为最佳诱变条件。采用三苯基氯化四氮唑(TTC)法和溴甲酚绿法以及杜氏小管筛选出产酒精和产酸强的目标菌株Y6-5,并对其遗传稳定性进行研究。结果表明,诱变菌株Y6-5与出发菌株Y6相比较,其产酒精、产酸能力分别提高了28.13%和201.41%,并且遗传稳定性良好。 相似文献
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Kitagaki H Kato T Isogai A Mikami S Shimoi H 《Journal of Bioscience and Bioengineering》2008,105(6):675-678
We previously demonstrated the presence and fragmentation of mitochondria during alcohol fermentation. Here, we show that Fis1p induces mitochondrial fragmentation, and inhibition of mitochondrial fragmentation causes higher malate production during sake brewing. These findings indicate that mitochondrial morphology affects the metabolism of constituents, providing a breeding strategy for high-malate-producing yeasts. 相似文献
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《Journal of the Institute of Brewing》2017,123(2):252-258
Screening of drug‐resistant mutants of sake yeast strains has been a major method for creation of superior strains. We attempted to create a valproic acid (VPA)‐resistant mutant strain from sake yeast Kyokai No. 7 (K7). VPA is a branched‐chain fatty acid and is an inositol synthesis inhibitor in mammals and yeast. We succeeded in isolating a mutant of strain K7 that can survive long‐term in a VPA‐containing medium. This strain, K7‐VPALS, is significantly more resistant to not only VPA‐induced cell death but also ethanol in comparison with the parent strain. Further experiments showed that the new strain is likely to have a deficiency in inositol and/or phosphatidylinositol synthesis. The major characteristics of sake brewed by strain K7‐VPALS (compared with K7) were lower amino acidity, higher isoamyl acetate content without an increase in the isoamyl alcohol level and changes in constituent organic acids, particularly higher malate and succinate but lower acetate concentrations. In addition, taste sensor analysis revealed that K7‐VPALS‐brewed sake has milder sourness and higher saltiness or richness than K7‐brewed sake does. High isoamyl acetate production may be related to a deficiency in phosphatidylinositol because this compound directly inhibits alcohol acetyltransferase, an enzyme responsible for isoamyl acetate synthesis. Strain K7‐VPALS grew more rapidly than the parental strain did in a medium containing acetate as a sole carbon source, indicating that K7‐VPALS effectively assimilates acetate and converts it to malate and succinate through the glyoxylate cycle. Thus, strain K7‐VPALS shows improved characteristics for brewing of high‐quality sake. Copyright © 2017 The Institute of Brewing & Distilling 相似文献
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Taku Katou Hiroshi Kitagaki Takeshi Akao Hitoshi Shimoi 《Yeast (Chichester, England)》2008,25(11):799-807
Sake yeast exhibit various characteristics that make them more suitable for sake brewing compared to other yeast strains. Since sake yeast strains are Saccharomyces cerevisiae heterothallic diploid strains, it is likely that they have heterozygous alleles on homologous chromosomes (heterozygosity) due to spontaneous mutations. If this is the case, segregation of phenotypic traits in haploid strains after sporulation and concomitant meiosis of sake yeast strains would be expected to occur. To examine this hypothesis, we isolated 100 haploid strains from Kyokai No. 7 (K7), a typical sake yeast strain in Japan, and compared their brewing characteristics in small‐scale sake‐brewing tests. Analyses of the resultant sake samples showed a smooth and continuous distribution of analytical values for brewing characteristics, suggesting that K7 has multiple heterozygosities that affect brewing characteristics and that these heterozygous alleles do segregate after sporulation. Correlation and principal component analyses suggested that the analytical parameters could be classified into two groups, indicating fermentation ability and sake flavour. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
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乙醇对细胞的抑制主要表现在对生长率、发酵率、糖分解酶、膜势能的抑制及膜磷脂的裂解,主要阐述了渗透压和温度对酒精酵母产生乙醇耐性的影响。 相似文献
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The mitochondrial states and activities of production yeasts used in the fermentation industry vary according to the availability of oxygen, size of the fermentation tank and temperature of the raw material. However, the involvement of the mitochondrial states of these yeasts in the production profile of organic acids during alcoholic fermentation has not been investigated in detail. In this study, the effects of the mitochondrial state of a sake brewing yeast on the organic acid production profile during an alcoholic fermentation process were investigated. It was elucidated that the mitochondrial state during the propagation stage significantly affected the mitochondrial morphology and the organic acid production profile during the alcoholic fermentation. When yeast mitochondria were active, they were highly branched in the propagation stage, and the yeast cells produced significantly more succinate and less malate. In contrast, when the yeast mitochondria were inactive, they were long and filamentous in appearance, and the yeast produced significantly less succinate and more malate. The change in malic acid content was reversed when an uncoupler of mitochondrial membrane potential, carbonylcyanide p‐trifluoromethoxyphenylhydrazone, was added to the culture, indicating that the change in the organic acid production profile could be attributed to mitochondrial activity. Furthermore, the content of malic acid and succinic acid could be converted from a respirative to a fermentative profile by exposing the yeast to a mitochondrion‐inactivating environment for 12 or 24 h. Taken together, it was shown that the mitochondrial status of the yeast affects malic acid production during alcoholic fermentation. Copyright © 2012 The Institute of Brewing & Distilling 相似文献