1. The response mechanism analysis of HMX1 knockout strain to levulinic acid in Saccharomyces cerevisiae
- Author
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Jiaye Tang, Yulei Chen, Qian Li, Wenli Xin, Ximeng Xiao, Xuemei Chen, Lixi Yang, Borui Mou, Jialian Li, Fujia Lu, Chun Fu, Wencong Long, Hong Liao, Xuebing Han, Peng Feng, Wei Li, Kedi Zhou, Liuyun Yang, Yaojun Yang, Menggen Ma, and Hanyu Wang
- Subjects
saccharomyces cerevisiae ,levulinic acid ,response mechanism ,transcriptome ,metabolome ,Microbiology ,QR1-502 - Abstract
Levulinic acid, a hydrolysis product of lignocellulose, can be metabolized into important compounds in the field of medicine and pesticides by engineered strains of Saccharomyces cerevisiae. Levulinic acid, as an intermediate product widely found in the conversion process of lignocellulosic biomass, has multiple applications. However, its toxicity to Saccharomyces cerevisiae reduces its conversion efficiency, so screening Saccharomyces cerevisiae genes that can tolerate levulinic acid becomes the key. By creating a whole-genome knockout library and bioinformatics analysis, this study used the phenotypic characteristics of cells as the basis for screening and found the HMX1 gene that is highly sensitive to levulinic acid in the oxidative stress pathway. After knocking out HMX1 and treating with levulinic acid, the omics data of the strain revealed that multiple affected pathways, especially the expression of 14 genes related to the cell wall and membrane system, were significantly downregulated. The levels of acetyl-CoA and riboflavin decreased by 1.02-fold and 1.44-fold, respectively, while the content of pantothenic acid increased. These findings indicate that the cell wall-membrane system, as well as the metabolism of acetyl-CoA and riboflavin, are important in improving the resistance of Saccharomyces cerevisiae to levulinic acid. They provide theoretical support for enhancing the tolerance of microorganisms to levulinic acid, which is significant for optimizing the conversion process of lignocellulosic biomass to levulinic acid.
- Published
- 2024
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