4.3 Article

Utilization of ethanol for itaconic acid biosynthesis by engineered Saccharomyces cerevisiae

Journal

FEMS YEAST RESEARCH
Volume 21, Issue 6, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/femsyr/foab043

Keywords

ethanol; acetic acid; AAC2; Saccharomyces cerevisiae; itaconic acid

Funding

  1. China National Key Research and Development Program [2019YFA0904300]

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This study investigated the metabolic regulation of ethanol utilization for itaconic acid production in Saccharomyces cerevisiae, highlighting the importance of mitochondrial membrane transporter proteins in the process. Upregulating the major ADP/ATP carrier AAC2 was found to accelerate ethanol utilization and itaconic acid production. RNA sequencing results indicated that AAC2 overexpression enhanced IA production by upregulating specific pathways in mitochondrial membrane, while exogenous aconitase expression did not increase IA production but affected ethanol utilization and cell growth. Ethanol metabolism in Saccharomyces cerevisiae is closely related to itaconic acid production.
In Saccharomyces cerevisiae, ethanol can serve as both a carbon source and NADH donor for the production of acetyl-CoA derivatives. Here we investigated the metabolic regulation of ethanol utilization for itaconic acid production by S. cerevisiae. To understand the interconnection between the TCA cycle and the glyoxylate pathway, mitochondrial membrane transporter proteins SFC1, YHM2, CTP1, DIC1 and MPC1 were knocked out and results showed that SFC1 functions as an important entrance of the glyoxylate pathway into the TCA cycle, and YHM2 is helpful to IA production but not the primary pathway for citric acid supply. To decrease the accumulation of acetic acid, the major ADP/ATP carrier of the mitochondrial inner membrane, AAC2, was upregulated and determined to accelerate ethanol utilization and itaconic acid production. RNA sequencing results showed that AAC2 overexpression enhanced IA titer by upregulating the ethanol-acetyl-CoA pathway and NADH oxidase in the mitochondrial membrane. RNA-seq analysis also suggested that aconitase ACO1 may be a rate-limiting step of IA production. However, the expression of exogenous aconitase didn't increase IA production but enhanced the rate of ethanol utilization and decreased cell growth. Ethanol metabolism in Saccharomyces cerevisiae related to itaconic acid production.

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