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Activation of futile cycles as an approach to increase ethanol yield during glucose fermentation in Saccharomyces cerevisiae

机译:无效循环的激活作为增加酿酒酵母葡萄糖发酵过程中乙醇产量的一种方法

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An increase in ethanol yield by yeast from the fermentation of conventional sugars such as glucose and sucrose is possible by reducing the production of a key byproduct such as cellular biomass. Previously we have reported that overexpression of PH08gene encoding non-specific ATP-hydrolyzing alkaline phosphatase can lead to a decrease in cellular ATP content and to an increase in ethanol yield during glucose fermentation by Saccharomyces cerevisiae. In this work we further report on 2 new successfulapproaches to reduce cellular levels of ATP that increase ethanol yield and productivity. The first approach is based on the overexpression of the heterologous Escherichia coli apy gene encoding apyrase or SSB1 part of the chaperon that exhibit ATPase activity in yeast. In the second approach we constructed a futile cycle by the overexpression of S. cerevisiae genes encoding pyruvate carboxylase and phosphoenolpyruvate carboxykinase in S. cerevisiae. These genetically engineered strains accumulated more ethanol compared to the wild-type strain during alcoholic fermentation.
机译:通过减少关键副产物(例如细胞生物质)的产生,可以通过酵母从常规糖(例如葡萄糖和蔗糖)的发酵中提高乙醇的产量。以前我们已经报道过编码非特异性ATP水解碱性磷酸酶的PH08基因的过表达可以导致酿酒酵母在葡萄糖发酵过程中细胞ATP含量的减少和乙醇产量的增加。在这项工作中,我们进一步报告了两种新的成功方法,这些方法可以降低ATP的细胞水平,从而增加乙醇的产量和生产率。第一种方法是基于异源大肠杆菌apy基因的过表达,该基因编码在酵母中具有ATPase活性的伴侣蛋白的Apyrase或SSB1部分。在第二种方法中,我们通过在啤酒酵母中过量表达编码丙酮酸羧化酶和磷酸烯醇丙酮酸羧化激酶的啤酒酵母基因来构建无效的循环。与酒精发酵过程中的野生型菌株相比,这些基因工程菌株积累了更多的乙醇。

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