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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 Dans Zh | WPRIM | ID: wpr-1007959
Responsable en Bibliothèque : 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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Texte intégral: 1 Indice: WPRIM Sujet Principal: Carbone / Protéines de transport / Hydroxymethyl et formyl transferases / Cystéine / Protéines Escherichia coli / Methylenetetrahydrofolate reductase (NADPH2) / Escherichia coli / Méthionine Limites du sujet: Humans langue: Zh Texte intégral: Chinese Journal of Biotechnology Année: 2023 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Carbone / Protéines de transport / Hydroxymethyl et formyl transferases / Cystéine / Protéines Escherichia coli / Methylenetetrahydrofolate reductase (NADPH2) / Escherichia coli / Méthionine Limites du sujet: Humans langue: Zh Texte intégral: Chinese Journal of Biotechnology Année: 2023 Type: Article