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Overexpression of endogenous stress-tolerance related genes in Saccharomyces cerevisiae improved strain robustness and production of heterologous cellobiohydrolase

机译:酿酒酵母中内源性胁迫性耐受性基因的过度表达改善了异源纤维素水解酶的应变鲁棒性和生产

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To enable Saccharomyces cerevisiae to produce renewable fuels from lignocellulose in a consolidated bioprocess, a heterologous cellulase system must be engineered into this yeast. In addition, inherently low secretion titers and sensitivity to adverse environmental conditions must be overcome. Here, two native S. cerevisiae genes related to yeast stress tolerance, YHB1 and SET5, were overexpressed under transcriptional control of the constitutive PGK1 promoter and their effects on heterologous secretion of Talaromyces emersonii cel7A cellobiohydrolase was investigated. Transformants showed increased secreted enzyme activity that ranged from 22% to 55% higher compared to the parental strains and this did not lead to deleterious growth effects. The recombinant strains overexpressing either YHB1 or SET5 also demonstrated multi-tolerant characteristics desirable in bioethanol production, i.e. improved tolerance to osmotic and heat stress. Quantitative reverse transcriptase PCR analysis in these strains showed decreased transcription of secretion pathway genes. However, decreased unfolded protein response was also observed, suggesting novel mechanisms for enhancing enzyme production through stress modulation. Overexpression of YHB1 in an unrelated diploid strain also enhanced stress tolerance and improved ethanol productivity in medium containing acetic acid. To our knowledge, this is the first demonstration that improved heterologous secretion and environmental stress tolerance could be engineered into yeast simultaneously.
机译:为了使Saccharomyces酿酒酵母从综合生物过程中产生从木质纤维素生产可再生燃料,必须将异源纤维素酶系统设计成该酵母。此外,必须克服固有的低分泌滴度和对不利环境条件的敏感性。这里,研究了与酵母胁迫耐受性,YHB1和Set5相关的两种天然S.酿酒酵母基因在组成型PGK1启动子的转录控制下过表达,并研究了对塔拉莫西氏菌麦克罗斯基纤维糖酶的异源分泌的影响。转化体显示出增加的分泌酶活性,与父母菌株相比,从22%达到55%,这不会导致有害生长效应。过表达YHB1或Set5的重组菌株还表现出在生物乙醇生产中所需的多耐受特性,即改善对渗透和热应激的耐受性。这些菌株中的定量逆转录酶PCR分析表明分泌途径基因的转录减少。然而,还观察到降低展开的蛋白质反应,表明通过应激调节提高酶产生的新机制。在不相关的二倍体菌株中的YHB1的过度表达也增强了含乙酸培养基中的应力耐受性和改善乙醇生产率。据我们所知,这是第一次改善异源分泌和环境胁迫耐受性同时工程化的演示。

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