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Re-assessment of YAP1 and MCR1 contributions to inhibitor tolerance in robust engineered Saccharomyces cerevisiae fermenting undetoxified lignocellulosic hydrolysate

机译:重新评估YAP1和MCR1在强大的工程酿酒酵母发酵未过氧化的木质纤维素水解物中对抑制剂耐受性的贡献

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Development of robust yeast strains that can efficiently ferment lignocellulose-based feedstocks is one of the requirements for achieving economically feasible bioethanol production processes. With this goal, several genes have been identified as promising candidates to confer improved tolerance to S. cerevisiae. In most of the cases, however, the evaluation of the genetic modification was performed only in laboratory strains, that is, in strains that are known to be quite sensitive to various types of stresses. In the present study, we evaluated the effects of overexpressing genes encoding the transcription factor (YAP1) and the mitochondrial NADH-cytochrome b5 reductase (MCR1), either alone or in combination, in an already robust and xylose-consuming industrial strain of S. cerevisiae and evaluated the effect during the fermentation of undiluted and undetoxified spruce hydrolysate. Overexpression of either gene resulted in faster hexose catabolism, but no cumulative effect was observed with the simultaneous overexpression. The improved phenotype of MCR1 overexpression appeared to be related, at least in part, to a faster furaldehyde reduction capacity, indicating that this reductase may have a wider substrate range than previously reported. Unexpectedly a decreased xylose fermentation rate was also observed in YAP1 overexpressing strains and possible reasons behind this phenotype are discussed.
机译:能够有效发酵木质纤维素基原料的健壮酵母菌株的开发是实现经济可行的生物乙醇生产工艺的要求之一。为了这个目标,已经鉴定了几种基因,它们有望赋予啤酒酵母更好的耐受性。然而,在大多数情况下,仅在实验室菌株中,即在已知对各种类型的胁迫非常敏感的菌株中,进行遗传修饰的评估。在本研究中,我们评估了过度表达编码转录因子(YAP1)和线粒体NADH-细胞色素b5还原酶(MCR1)的基因在已经健壮且消耗木糖的S菌株中的作用。酸并评估未稀释和未脱氧的云杉水解产物发酵过程中的效果。任一基因的过表达导致更快的己糖分解代谢,但同时过表达未观察到累积效应。 MCR1过表达的改善表型似乎至少部分地与更快的呋喃醛还原能力有关,表明该还原酶的底物范围可能比以前报道的要宽。出乎意料的是,在过表达YAP1的菌株中还观察到木糖发酵速率降低,并讨论了该表型背后的可能原因。

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