DOE Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, 53726, Madison, WI, United States.
Laboratory of Genetics, University of Wisconsin-Madison, 53706, Madison, WI, United States.
FEMS Yeast Res. 2022 Sep 24;21(1). doi: 10.1093/femsyr/foac036.
The budding yeast Saccharomyces cerevisiae has been used extensively in fermentative industrial processes, including biofuel production from sustainable plant-based hydrolysates. Myriad toxins and stressors found in hydrolysates inhibit microbial metabolism and product formation. Overcoming these stresses requires mitigation strategies that include strain engineering. To identify shared and divergent mechanisms of toxicity and to implicate gene targets for genetic engineering, we used a chemical genomic approach to study fitness effects across a library of S. cerevisiae deletion mutants cultured anaerobically in dozens of individual compounds found in different types of hydrolysates. Relationships in chemical genomic profiles identified classes of toxins that provoked similar cellular responses, spanning inhibitor relationships that were not expected from chemical classification. Our results also revealed widespread antagonistic effects across inhibitors, such that the same gene deletions were beneficial for surviving some toxins but detrimental for others. This work presents a rich dataset relating gene function to chemical compounds, which both expands our understanding of plant-based hydrolysates and provides a useful resource to identify engineering targets.
酿酒酵母(Saccharomyces cerevisiae)已广泛应用于发酵工业过程中,包括利用可持续的植物水解物生产生物燃料。水解物中存在的许多毒素和应激源会抑制微生物代谢和产物形成。克服这些压力需要缓解策略,包括菌株工程。为了确定毒性的共同和不同机制,并确定遗传工程的基因靶标,我们使用化学基因组学方法研究了在不同类型水解物中发现的数十种单一化合物中厌氧培养的酿酒酵母缺失突变体文库中的适应性效应。化学基因组图谱中的关系确定了引起相似细胞反应的毒素类别,涵盖了化学分类中未预期到的抑制剂关系。我们的结果还揭示了抑制剂之间广泛的拮抗作用,使得相同的基因突变缺失对某些毒素有益,但对其他毒素有害。这项工作提供了一个与化学化合物相关的丰富的基因功能数据集,既扩展了我们对植物基水解物的理解,又为鉴定工程目标提供了有用的资源。