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一株过量产生甘露糖蛋白的重组酿酒酵母菌株可使葡萄酒对蛋白质浑浊具有稳定性。

A recombinant Saccharomyces cerevisiae strain overproducing mannoproteins stabilizes wine against protein haze.

作者信息

Gonzalez-Ramos Daniel, Cebollero Eduardo, Gonzalez Ramon

机构信息

Department of Microbiology, Instituto de Fermentaciones Industriales (CSIC), Juan de la Cierva 3, 28006 Madrid, Spain.

出版信息

Appl Environ Microbiol. 2008 Sep;74(17):5533-40. doi: 10.1128/AEM.00302-08. Epub 2008 Jul 7.

Abstract

Stabilization against protein haze was one of the first positive properties attributed to yeast mannoproteins in winemaking. In previous work we demonstrated that deletion of KNR4 leads to increased mannoprotein release in laboratory Saccharomyces cerevisiae strains. We have now constructed strains with KNR4 deleted in two different industrial wine yeast backgrounds. This required replacement of two and three alleles of KNR4 for the EC1118 and T73-4 backgrounds, respectively, and the use of three different selection markers for yeast genetic transformation. The actual effect of the genetic modification was dependent on both the genetic background and the culture conditions. The fermentation performance of T73-4 derivatives was clearly impaired, and these derivatives did not contribute to the protein stability of the wine, even though they showed increased mannoprotein release in vitro. In contrast, the EC1118 derivative with both alleles of KNR4 deleted released increased amounts of mannoproteins both in vitro and during wine fermentation assays, and the resulting wines were consistently less susceptible to protein haze. The fermentation performance of this strain was slightly impaired, but only with must with a very high sugar content. These results pave the way for the development of new commercial strains with the potential to improve several mannoprotein-related quality and technological parameters of wine.

摘要

抗蛋白质浑浊稳定性是酿酒中酵母甘露糖蛋白最早被发现的积极特性之一。在之前的研究中,我们证明了在实验室酿酒酵母菌株中敲除KNR4会导致甘露糖蛋白释放增加。我们现在构建了在两种不同的工业葡萄酒酵母背景下敲除KNR4的菌株。对于EC1118和T73 - 4背景,分别需要替换两个和三个KNR4等位基因,并使用三种不同的选择标记进行酵母遗传转化。基因改造的实际效果取决于遗传背景和培养条件。T73 - 4衍生物的发酵性能明显受损,这些衍生物对葡萄酒的蛋白质稳定性没有贡献,尽管它们在体外显示出甘露糖蛋白释放增加。相比之下,敲除两个KNR4等位基因的EC1118衍生物在体外和葡萄酒发酵试验中都释放出更多的甘露糖蛋白,并且所得到的葡萄酒对蛋白质浑浊的敏感性始终较低。该菌株的发酵性能略有受损,但仅在糖分含量非常高的葡萄汁中如此。这些结果为开发具有改善葡萄酒几个与甘露糖蛋白相关的质量和技术参数潜力的新型商业菌株铺平了道路。

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