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Potential Application of the Oryza sativa Monodehydroascorbate Reductase Gene (OsMDHAR) to Improve the Stress Tolerance and Fermentative Capacity of Saccharomyces cerevisiae

机译:水稻单脱氢抗坏血酸还原酶基因(OsMDHAR)在提高酿酒酵母抗逆性和发酵能力方面的潜在应用

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摘要

Monodehydroascorbate reductase (MDHAR; EC 1.6.5.4) is an important enzyme for ascorbate recycling. To examine whether heterologous expression of MDHAR from Oryza sativa (OsMDHAR) can prevent the deleterious effects of unfavorable growth conditions, we constructed a transgenic yeast strain harboring a recombinant plasmid carrying OsMDHAR (p426GPD::OsMDHAR). OsMDHAR-expressing yeast cells displayed enhanced tolerance to hydrogen peroxide by maintaining redox homoeostasis, proteostasis, and the ascorbate (AsA)-like pool following the accumulation of antioxidant enzymes and molecules, metabolic enzymes, and molecular chaperones and their cofactors, compared to wild-type (WT) cells carrying vector alone. The addition of exogenous AsA or its analogue isoascorbic acid increased the viability of WT and ara2Δ cells under oxidative stress. Furthermore, the survival of OsMDHAR-expressing cells was greater than that of WT cells when cells at mid-log growth phase were exposed to high concentrations of ethanol. High OsMDHAR expression also improved the fermentative capacity of the yeast during glucose-based batch fermentation at a standard cultivation temperature (30°C). The alcohol yield of OsMDHAR-expressing transgenic yeast during fermentation was approximately 25% (0.18 g·g-1) higher than that of WT yeast. Accordingly, OsMDHAR-expressing transgenic yeast showed prolonged survival during the environmental stresses produced during fermentation. These results suggest that heterologous OsMDHAR expression increases tolerance to reactive oxygen species-induced oxidative stress by improving cellular redox homeostasis and improves survival during fermentation, which enhances fermentative capacity.
机译:单脱氢抗坏血酸还原酶(MDHAR; EC 1.6.5.4)是抗坏血酸循环的重要酶。为了检查来自水稻的MDHAR(OsMDHAR)的异源表达是否可以防止不利生长条件的有害影响,我们构建了带有携带OsMDHAR(p426GPD :: OsMDHAR)重组质粒的转基因酵母菌株。相比于野生型,表达OsMDHAR的酵母细胞在抗氧化剂酶和分子,代谢酶,分子伴侣及其辅因子积累之后,通过维持氧化还原同位,蛋白稳态和抗坏血酸(AsA)样池,显示出对过氧化氢的增强耐受性。型(WT)细胞仅携带载体。外源AsA或其类似物异抗坏血酸的添加提高了氧化应激下WT和ara2Δ细胞的活力。此外,当处于对数生长期中期的细胞暴露于高浓度的乙醇中时,表达OsMDHAR的细胞的存活率比野生型细胞的存活率高。 OsMDHAR的高表达还改善了在标准培养温度(30°C)下基于葡萄糖的分批发酵过程中酵母的发酵能力。在发酵过程中,表达OsMDHAR的转基因酵母的酒精产量比WT酵母高约25%(0.18 g·g -1 )。因此,表达OsMDHAR的转基因酵母在发酵过程中产生的环境压力期间显示出延长的生存期。这些结果表明,异源OsMDHAR表达通过改善细胞氧化还原稳态而增加了对活性氧诱导的氧化应激的耐受性,并改善了发酵期间的存活率,从而增强了发酵能力。

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