牛奶经多次发酵后的酒精发酵

Yoshihisa Wakita, H. Kanda, Koji Takazumi, Y. Tsuchiya
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摘要

酿酒酵母是一种用于酒精生产的代表性酵母。利用酿酒酵母从牛奶中生产酒精并不容易,因为这种细菌不能水解乳糖。德尔布鲁氏乳杆菌亚种保加利亚菌(LDB)能够将乳糖水解成半乳糖和葡萄糖,广泛用于酸奶生产。在本研究中,利用酿酒酵母和LDB进行多次发酵,以牛奶为原料生产酒精。首先,通过n -甲基-n ' -硝基-n -亚硝基胍诱变LDB48P获得了分解代谢抑制释放的菌株LDB48A-12。LDB48A-12具有较高的乳糖降解能力。令人惊讶的是,LDB48A-12的生长速度和乳酸产量低于LDB48P。用LDB48A-12和酿酒酵母SBC3207在30℃或37℃下发酵4天,10%脱脂乳溶液的酒精产量约为1~1.5%,是用LDB48P发酵的1.5倍。此外,pH值的下降也被抑制。这些结果被认为证明了新的酒精牛奶发酵。基因组序列比较发现LDB48A-12中存在RpoA和DnaA突变。这些基因分别与分解代谢物抑制和基因组DNA复制有关,表明这些基因的组合突变导致了酒精牛奶发酵的有利表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alcohol fermentation of milk by multiple fermentation
Saccharomyces cerevisiae is a representative yeast used for alcohol production. Production of alcohol from milk using S. cerevisiae is not easy, as this species is unable to hydrolyse lactose. Lactobacillus delbrueckii subsp. bulgaricus (LDB) is able to hydrolyse lactose into galactose and glucose, and is widely used in yogurt production. In this study, production of alcohol from milk was attempted by multiple fermentation using S. cerevisiae and LDB. Firstly, strain LDB48A-12, released from catabolite repression, was obtained from LDB48P by N-methyl-N ’-nitro-N-nitrosoguanidine mutagenesis. LDB48A-12 showed high ability of lactose degradation. Surprisingly, growth speed and lactate production of LDB48A-12 were found to be lower than those of LDB48P. Fermentation of 10% skim milk solution using LDB48A-12 and S. cerevisiae SBC3207 for 4 days at 30℃ or 37℃ produced approximately 1~1.5% of alcohol, which was 1.5 times that produced using LDB48P. In addition, decrease in pH was inhibited. These results were thought to demonstrate novel alcoholic milk fermentation. Comparison of genome sequences revealed mutations in RpoA and DnaA in LDB48A-12. These genes are related to catabolite repression and replication of genome DNA, respectively, suggesting that combined mutation of these genes leads to the preferable phenotype for alcoholic milk fermentation.
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