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首页> 外文期刊>Microbial Cell Factories >Transcription analysis of recombinant industrial and laboratory Saccharomyces cerevisiae strains reveals the molecular basis for fermentation of glucose and xylose
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Transcription analysis of recombinant industrial and laboratory Saccharomyces cerevisiae strains reveals the molecular basis for fermentation of glucose and xylose

机译:重组工业和实验室酿酒酵母菌株的转录分析揭示了葡萄糖和木糖发酵的分子基础

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Background There has been much research on the bioconversion of xylose found in lignocellulosic biomass to ethanol by genetically engineered Saccharomyces cerevisiae. However, the rate of ethanol production from xylose in these xylose-utilizing yeast strains is quite low compared to their glucose fermentation. In this study, two diploid xylose-utilizing S. cerevisiae strains, the industrial strain MA-R4 and the laboratory strain MA-B4, were employed to investigate the differences between anaerobic fermentation of xylose and glucose, and general differences between recombinant yeast strains, through genome-wide transcription analysis. Results In MA-R4, many genes related to ergosterol biosynthesis were expressed more highly with glucose than with xylose. Additionally, these ergosterol-related genes had higher transcript levels in MA-R4 than in MA-B4 during glucose fermentation. During xylose fermentation, several genes related to central metabolic pathways that typically increase during growth on non-fermentable carbon sources were expressed at higher levels in both strains. Xylose did not fully repress the genes encoding enzymes of the tricarboxylic acid and respiratory pathways, even under anaerobic conditions. In addition, several genes involved in spore wall metabolism and the uptake of ammonium, which are closely related to the starvation response, and many stress-responsive genes mediated by Msn2/4p, as well as trehalose synthase genes, increased in expression when fermenting with xylose, irrespective of the yeast strain. We further observed that transcript levels of genes involved in xylose metabolism, membrane transport functions, and ATP synthesis were higher in MA-R4 than in MA-B4 when strains were fermented with glucose or xylose. Conclusions Our transcriptomic approach revealed the molecular events underlying the response to xylose or glucose and differences between MA-R4 and MA-B4. Xylose-utilizing S. cerevisiae strains may recognize xylose as a non-fermentable carbon source, which induces a starvation response and adaptation to oxidative stress, resulting in the increased expression of stress-response genes.
机译:背景技术关于通过基因工程酿酒酵母将木质纤维素生物质中发现的木糖生物转化为乙醇的研究很多。然而,与它们的葡萄糖发酵相比,在这些利用木糖的酵母菌株中从木糖生产乙醇的速率非常低。在这项研究中,使用了两个利用二倍体木糖的酿酒酵母菌株,工业菌株MA-R4和实验室菌株MA-B4,研究了木糖和葡萄糖的厌氧发酵之间的差异,以及重组酵母菌株之间的一般差异,通过全基因组转录分析。结果在MA-R4中,与麦角固醇生物合成相关的许多基因在葡萄糖中的表达比木糖更高。此外,在葡萄糖发酵过程中,这些麦角固醇相关基因在MA-R4中的转录水平高于在MA-B4中。在木糖发酵过程中,与中央代谢途径有关的几个基因通常在非发酵碳源上生长期间增加,在两个菌株中均以较高的水平表达。木糖即使在厌氧条件下也不能完全抑制编码三羧酸和呼吸道酶的基因。此外,与饥饿反应密切相关的一些与孢子壁代谢和铵离子吸收有关的基因,以及由Msn2 / 4p介导的许多应激反应基因以及海藻糖合酶基因,在发酵时会增加表达。木糖,与酵母菌株无关。我们进一步观察到,当菌株用葡萄糖或木糖发酵时,MA-R4中涉及木糖代谢,膜转运功能和ATP合成的基因的转录水平高于MA-B4。结论我们的转录组方法揭示了对木糖或葡萄糖反应的分子事件以及MA-R4和MA-B4之间的差异。利用木糖的酿酒酵母菌株可以将木糖识别为不可发酵的碳源,其诱导饥饿反应和对氧化应激的适应,从而导致应激反应基因的表达增加。

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