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Increased expression of the yeast multidrug resistance ABC transporter Pdr18 leads to increased ethanol tolerance and ethanol production in high gravity alcoholic fermentation

机译:酵母多重耐药性ABC转运蛋白Pdr18的表达增加导致高重力酒精发酵中的乙醇耐受性和乙醇生产增加

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Background The understanding of the molecular basis of yeast tolerance to ethanol may guide the design of rational strategies to increase process performance in industrial alcoholic fermentations. A set of 21 genes encoding multidrug transporters from the ATP-Binding Cassette (ABC) Superfamily and Major Facilitator Superfamily (MFS) in S. cerevisiae were scrutinized for a role in ethanol stress resistance. Results A yeast multidrug resistance ABC transporter encoded by the PDR18 gene, proposed to play a role in the incorporation of ergosterol in the yeast plasma membrane, was found to confer resistance to growth inhibitory concentrations of ethanol. PDR18 expression was seen to contribute to decreased 3?H-ethanol intracellular concentrations and decreased plasma membrane permeabilization of yeast cells challenged with inhibitory ethanol concentrations. Given the increased tolerance to ethanol of cells expressing PDR18, the final concentration of ethanol produced during high gravity alcoholic fermentation by yeast cells devoid of PDR18 was lower than the final ethanol concentration produced by the corresponding parental strain. Moreover, an engineered yeast strain in which the PDR18 promoter was replaced in the genome by the stronger PDR5 promoter, leading to increased PDR18 mRNA levels during alcoholic fermentation, was able to attain a 6?% higher ethanol concentration and a 17?% higher ethanol production yield than the parental strain. The improved fermentative performance of yeast cells over-expressing PDR18 was found to correlate with their increased ethanol tolerance and ability to restrain plasma membrane permeabilization induced throughout high gravity fermentation. Conclusions PDR18 gene over-expression increases yeast ethanol tolerance and fermentation performance leading to the production of highly inhibitory concentrations of ethanol. PDR18 overexpression in industrial yeast strains appears to be a promising approach to improve alcoholic fermentation performance for sustainable bio-ethanol production.
机译:背景技术了解酵母对乙醇的耐受性的分子基础可能指导合理策略的设计,以提高工业酒精发酵中的工艺性能。研究了酿酒酵母中21个编码来自ATP结合盒(ABC)超家族和主要促进者超家族(MFS)的多药转运蛋白的基因,研究了其在乙醇胁迫抗性中的作用。结果发现,由PDR18基因编码的一种酵母多药抗性ABC转运蛋白被认为在麦角甾醇掺入酵母的质膜中发挥了作用,被发现对乙醇的生长抑制浓度具有抗性。 PDR18的表达有助于降低 3 ΔH-乙醇的细胞内浓度,并降低了受到抑制性乙醇浓度攻击的酵母细胞的质膜通透性。鉴于表达PDR18的细胞对乙醇的耐受性增强,不含PDR18的酵母细胞在高重力酒精发酵过程中产生的乙醇终浓度低于相应亲本菌株产生的乙醇终浓度。此外,一种工程改造的酵母菌株,其中在基因组中用更强的PDR5启动子代替了PDR18启动子,导致酒精发酵过程中PDR18 mRNA水平增加,能够使乙醇浓度提高6%,乙醇提高17%。产量比亲本菌株高。发现过表达PDR18的酵母细胞改善的发酵性能与其提高的乙醇耐受性和抑制在整个高重力发酵中诱导的质膜透化的能力相关。结论PDR18基因的过表达提高了酵母对乙醇的耐受性和发酵性能,导致产生了高抑制浓度的乙醇。工业酵母菌株中PDR18的过表达似乎是改善酒精发酵性能以实现可持续生物乙醇生产的有前途的方法。

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