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Efficient synthesis of L-methionine by engineering the one carbon module of Escherichia coli / 生物工程学报
Chinese Journal of Biotechnology ; (12): 3302-3317, 2023.
Article in Zh | WPRIM | ID: wpr-1007959
Responsible library: WPRO
ABSTRACT
L-methionine, also known as L-aminomethane, is one of the eight essential amino acids required by the human body and has important applications in the fields of feed, medicine, and food. In this study, an L-methionine high-yielding strain was constructed using a modular metabolic engineering strategy based on the M2 strain (Escherichia coli W3110 ΔIJAHFEBC/PAM) previously constructed in our laboratory. Firstly, the production of one-carbon module methyl donors was enhanced by overexpression of methylenetetrahydrofolate reductase (methylenetetrahydrofolate reductase, MetF) and screening of hydroxymethyltransferase (GlyA) from different sources, optimizing the one-carbon module. Subsequently, cysteamine lyase (hydroxymethyltransferase, MalY) and cysteine internal transporter gene (fliY) were overexpressed to improve the supply of L-homocysteine and L-cysteine, two precursors of the one-carbon module. The production of L-methionine in shake flask fermentation was increased from 2.8 g/L to 4.05 g/L, and up to 18.26 g/L in a 5 L fermenter. The results indicate that the one carbon module has a significant impact on the biosynthesis of L-methionine, and efficient biosynthesis of L-methionine can be achieved through optimizing the one carbon module. This study may facilitate further improvement of microbial fermentation production of L-methionine.
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Full text: 1 Database: WPRIM Main subject: Carbon / Carrier Proteins / Hydroxymethyl and Formyl Transferases / Cysteine / Escherichia coli Proteins / Methylenetetrahydrofolate Reductase (NADPH2) / Escherichia coli / Methionine Limits: Humans Language: Zh Journal: Chinese Journal of Biotechnology Year: 2023 Document type: Article
Full text: 1 Database: WPRIM Main subject: Carbon / Carrier Proteins / Hydroxymethyl and Formyl Transferases / Cysteine / Escherichia coli Proteins / Methylenetetrahydrofolate Reductase (NADPH2) / Escherichia coli / Methionine Limits: Humans Language: Zh Journal: Chinese Journal of Biotechnology Year: 2023 Document type: Article
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