乙酰丙酸胁迫下酿酒酵母关键基因LDH1敲除菌株对脂质降解的响应机制分析

IF 2.3 3区 生物学 Q3 MICROBIOLOGY
Yulei Chen, Jiaye Tang, Qian Li, Wenli Xin, Ximeng Xiao, Borui Mou, Jialian Li, Fujia Lu, Chun Fu, Wencong Long, Hong Liao, Xuebing Han, Peng Feng, Wei Li, Kedi Zhou, Liuyun Yang, Xuemei Chen, Lixi Yang, Menggen Ma, Yaojun Yang, Hanyu Wang
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引用次数: 0

摘要

乙酰丙酸(LA)是燃料乙醇生产中的主要有毒副产物,其大量排放对生态环境造成不利影响。为了有效去除废液中的LA,采用了微生物降解的方法,但面临的挑战是微生物不能完全耐受废液中的LA。因此,探索微生物对LA的耐受机制就显得尤为重要。本研究进行了全基因组敲除文库扫描和敏感敲除菌株鉴定。用2’7’-DCF双乙酸酯、Mito Tracker Green FM、液泡膜标记MDY-64、ER-Tracker Red染料等荧光染料染色后,在荧光显微镜下观察到线粒体、液泡、内质网等亚细胞结构及活性氧(ROS)积累。我们还对野生型菌株和敲除菌株进行了基因组测序。通过比较基因组分析发现,酿酒酵母中的LDH1 (YBR204C)基因有助于促进细胞内活性氧的清除,LDH1的缺失导致细胞膜、细胞壁和细胞周期相关基因下调2倍以上。通过测量LDH1敲除菌株(ldh1Δ)在LA胁迫下的转录组和代谢组,并与野生型菌株BY4741进行比较,我们发现在LDH1敲除的条件下,NAD+中间体的积累会被激活,破坏正常的细胞功能,造成细胞损伤。LDH1基因敲除也会影响细胞内的甲基循环,这与ROS的积累密切相关。这些研究结果为培育耐受性更高、降解效率更高、成本更低的酿酒酵母转基因菌株提供了可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the response mechanism in lipid degradation of key gene LDH1 knockout strains of Saccharomyces cerevisiae under levulinic acid stress.

Levulinic acid (LA) is the main toxic by-product in the production of fuel ethanol, and its large-scale emission adversely affect the ecological environment. In order to effectively remove LA from the liquid waste, microbial degradation methods are adopted but the challenge is that microorganisms cannot fully tolerate LA in the waste. Therefore, it is particularly important to explore the tolerance mechanism of microorganisms to LA. In this study, the whole-genome knockout library scanning and sensitive knockout strain identification were carried out. In addition, subcellular structures such as mitochondria, vacuoles, and endoplasmic reticulum as well as reactive oxygen species (ROS) accumulation were observed under a fluorescence microscopy after stained with fluorescent dyes such as 2'7'-DCF diacetate, Mito Tracker Green FM, Vacuole Membrane Marker MDY-64, and ER-Tracker Red dye. We also performed genomic sequencing on the wild-type strain and knockout strain. Through comparative genomic analysis, it's been found that the LDH1 (YBR204C) gene in Saccharomyces cerevisiae helps promote the clearance of intracellular reactive oxygen species, and the deletion of LDH1 leads to a more-than-two-fold down-regulation of genes related to cell membrane, cell wall, and cell cycle. By measuring the transcriptome and metabolome of the LDH1 knockout strain (ldh1Δ) under LA stress and comparing it with the wild-type strain BY4741, we found that under the condition of LDH1 knockout, the accumulation of NAD+ intermediates would be activated, disrupting normal cell functions and causing cell damage. The LDH1 gene knockout also affects the Methyl Cycle in the cell, which is closely related to the accumulation of ROS. These research results make it possible to create a new genetically modified strain of S. cerevisiae with desired higher tolerance which enhances degradation efficiency and reduces cost.

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来源期刊
Archives of Microbiology
Archives of Microbiology 生物-微生物学
CiteScore
4.90
自引率
3.60%
发文量
601
审稿时长
3 months
期刊介绍: Research papers must make a significant and original contribution to microbiology and be of interest to a broad readership. The results of any experimental approach that meets these objectives are welcome, particularly biochemical, molecular genetic, physiological, and/or physical investigations into microbial cells and their interactions with their environments, including their eukaryotic hosts. Mini-reviews in areas of special topical interest and papers on medical microbiology, ecology and systematics, including description of novel taxa, are also published. Theoretical papers and those that report on the analysis or ''mining'' of data are acceptable in principle if new information, interpretations, or hypotheses emerge.
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