Ehsani Maryam, Fernández Maria R, Biosca Josep A, Julien Anne, Dequin Sylvie
INRA, UMR 1083, F-34060 Montpellier, France.
Appl Environ Microbiol. 2009 May;75(10):3196-205. doi: 10.1128/AEM.02157-08. Epub 2009 Mar 27.
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 BDH1(221,222,223), 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 degrees.
过表达编码甘油-3-磷酸脱氢酶的GPD1且缺乏乙醛脱氢酶Ald6的工程酿酒酵母菌株,能够使碳通量从乙醇大规模转向甘油,且不会积累乙酸盐。尽管GPD1 ald6菌株在降低葡萄酒中乙醇含量方面具有很大潜力,但一个主要的副作用是乙偶姻的积累,这会对葡萄酒产生负面的感官影响。乙偶姻通过依赖NADH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,我们在过量产生甘油的葡萄酒酵母中过表达了编码天然依赖NADH的Bdh1的BDH1,以及编码氨基酸变化为221 EIA 223至221 SRS 223的依赖NADPH的Bdh1酶的工程基因BDH1(221,222,223)。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,主要的限制因素是Bdh1的合成水平。与这一发现一致,天然或工程化Bdh1的过量产生使得将85%至90%积累的乙偶姻重定向为2,3-丁二醇成为可能,2,3-丁二醇是一种具有中性感官特征的化合物。此外,在过量产生甘油的酵母细胞中产量增加的、导致酒精饮料产生异味的双乙酰的产量降低了一半。与对照细胞相比,GPD1 ald6细胞中高级醇和酯的产量略有下降或不变,在BDH1细胞中没有进一步改变。总体而言,将碳重定向到甘油和2,3-丁二醇代表了具有理想感官特性的低酒精酵母工程中的一个新里程碑,可以使葡萄酒中的乙醇含量降低多达3度。