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Engineering of 23-Butanediol Dehydrogenase To Reduce Acetoin Formation by Glycerol-Overproducing Low-Alcohol Saccharomyces cerevisiae

机译:23-丁二醇脱氢酶的工程以减少甘油的过量生产低酒精啤酒酵母的丙酮生成。

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摘要

Engineered Saccharomyces cerevisiae strains overexpressing GPD1, which codes for glycerol-3-phosphate dehydrogenase, and lacking the acetaldehyde dehydrogenase Ald6 display large-scale diversion of the carbon flux from ethanol toward glycerol without accumulating acetate. Although GPD1 ald6 strains have great potential for reducing the ethanol contents in wines, one major side effect is the accumulation of acetoin, having a negative sensory impact on wine. Acetoin is reduced to 2,3-butanediol by the NADH-dependent 2,3-butanediol dehydrogenase Bdh1. In order to investigate the influence of potential factors limiting this reaction, we overexpressed BDH1, coding for native NADH-dependent Bdh1, and the engineered gene BDH1221,222,223, coding for an NADPH-dependent Bdh1 enzyme with the amino acid changes 221 EIA 223 to 221 SRS 223, in a glycerol-overproducing wine yeast. We have shown that both the amount of Bdh1 and the NADH availability limit the 2,3-butanediol dehydrogenase reaction. During wine fermentation, however, the major limiting factor was the level of synthesis of Bdh1. Consistent with this finding, the overproduction of native or engineered Bdh1 made it possible to redirect 85 to 90% of the accumulated acetoin into 2,3-butanediol, a compound with neutral sensory characteristics. In addition, the production of diacetyl, a compound causing off-flavor in alcoholic beverages, whose production is increased in glycerol-overproducing yeast cells, was decreased by half. The production of higher alcohols and esters, which was slightly decreased or unchanged in GPD1 ald6 cells compared to that in the control cells, was not further modified in BDH1 cells. Overall, rerouting carbons toward glycerol and 2,3-butanediol represents a new milestone in the engineering of a low-alcohol yeast with desirable organoleptic features, permitting the decrease of the ethanol contents in wines by up to 3°.
机译:工程化的酿酒酵母菌株过表达GPD1,该菌株编码3-磷酸甘油脱氢酶,而缺少乙醛脱氢酶Ald6,显示碳通量从乙醇向甘油的大规模转移,而不会积累乙酸盐。尽管GPD1 ald6菌株具有降低葡萄酒中乙醇含量的巨大潜力,但一个主要的副作用是丙酮酸的积累,对葡萄酒产生负面的感官影响。乙酰乙酸被NADH依赖性的2,3-丁二醇脱氢酶Bdh1还原为2,3-丁二醇。为了研究限制该反应的潜在因素的影响,我们过表达了编码天然NADH依赖性Bdh1的BDH1和编码具有NADPH依赖性Bdh1酶的工程基因BDH1221,222,223,其氨基酸变化为221 EIA 223至221 SRS 223,在生产甘油的葡萄酒酵母中。我们已经表明,Bdh1的量和NADH的可用性都限制了2,3-丁二醇脱氢酶反应。然而,在葡萄酒发酵过程中,主要限制因素是Bdh1的合成水平。与该发现一致的是,天然或工程化的Bdh1的过量生产使得将积累的85-90%的乙酰丁香精重定向到2,3-丁二醇(一种具有中性感官特征的化合物)中成为可能。另外,二乙酰基的产量减少了一半,而二乙酰基的含量降低了一半,该化合物在酒精饮料中引起异味,而后者在甘油过剩的酵母细胞中的生成量增加。与对照细胞相比,GPD1 ald6细胞中的高级醇和酯的产量略有降低或保持不变,但在BDH1细胞中并未进一步修饰。总体而言,将碳改向甘油和2,3-丁二醇代表了具有理想感官特性的低酒精酵母工程化的新里程碑,可将葡萄酒中的乙醇含量降低多达3°。

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