CRISPRi筛选突出了酿酒酵母中涉及甲酸耐受性的染色质调节

Vaskar Mukherjee , Ibai Lenitz , Ulrika Lind , Anders Blomberg , Yvonne Nygård
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引用次数: 1

摘要

甲酸是木质纤维素水解物中的主要弱酸之一,即使在低浓度下也能抑制酵母的生长。在这项研究中,我们使用了一个包含9000个菌株的CRISPR干扰(CRISPRi)菌株文库,其中包含98%的必需和呼吸生长必需基因,来研究酿酒酵母的甲酸耐受性。为了提供甲酸耐受性的定量生长估计,使用Scan-o-Matic平台在补充140 mM甲酸的固体培养基上对菌株进行单独筛选。选择的耐药和敏感菌株在添加甲酸的液体培养基和含有抑制剂组合的合成水解液培养基中进行鉴定。具有靶向染色质重塑相关基因的gRNAs的菌株在具有甲酸耐受性的菌株中显著富集。与早期对乙酸耐受性的研究结果一致,我们发现在甲酸敏感菌株中,编码参与细胞内囊泡运输的蛋白质的基因丰富。菌株在合成水解液培养基中的生长趋势与在添加甲酸培养基中的生长趋势相同。对甲酸敏感的菌株在合成水解液中生长下降,而在甲酸存在下生长改善的菌株在水解液中也生长良好。对CRISPRi菌株进行系统分析,可以识别参与耐受性机制的基因,并为对木质纤维素水解物抑制剂具有更高抗性的生物工程菌株提供新的工程靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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CRISPRi screen highlights chromatin regulation to be involved in formic acid tolerance in Saccharomyces cerevisiae

Formic acid is one of the main weak acids in lignocellulosic hydrolysates that is known to be inhibitory to yeast growth even at low concentrations. In this study, we employed a CRISPR interference (CRISPRi) strain library comprising >9000 strains encompassing >98% of all essential and respiratory growth-essential genes, to study formic acid tolerance in Saccharomyces cerevisiae. To provide quantitative growth estimates on formic acid tolerance, the strains were screened individually on solid medium supplemented with 140 mM formic acid using the Scan-o-Matic platform. Selected resistant and sensitive strains were characterized in liquid medium supplemented with formic acid and in synthetic hydrolysate medium containing a combination of inhibitors. Strains with gRNAs targeting genes associated with chromatin remodeling were significantly enriched for strains showing formic acid tolerance. In line with earlier findings on acetic acid tolerance, we found genes encoding proteins involved in intracellular vesicle transport enriched among formic acid sensitive strains. The growth of the strains in synthetic hydrolysate medium followed the same trend as when screened in medium supplemented with formic acid. Strains sensitive to formic acid had decreased growth in the synthetic hydrolysate and all strains that had improved growth in the presence of formic acid also grew better in the hydrolysate medium. Systematic analysis of CRISPRi strains allowed identification of genes involved in tolerance mechanisms and provided novel engineering targets for bioengineering strains with increased resistance to inhibitors in lignocellulosic hydrolysates.

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