4.7 Article

Rerouting Fluxes of the Central Carbon Metabolism and Relieving Mechanism-Based Inactivation of L-Aspartate-α-decarboxylase for Fermentative Production of β-Alanine in Escherichia coli

Journal

ACS SYNTHETIC BIOLOGY
Volume 11, Issue 5, Pages 1908-1918

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssynbio.2c00055

Keywords

beta-alanine; central carbon metabolism; fed-batch bioprocess optimization; mechanism-based inactivation

Funding

  1. National Key Research and Development Program of China [2018YFA0901400]

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In this study, a high-yield beta-alanine-producing strain was constructed using metabolic engineering, protein engineering, and fed-batch bioprocess optimization strategies. The optimized strain achieved high productivity and yield, making it valuable for industrial production of beta-alanine and its derivatives.
beta-Alanine, with the amino group at the beta-position, is an important platform chemical that has been widely applied in pharmaceuticals and feed and food additives. However, the current modest titer and productivity, increased fermentation cost, and complicated operation are the challenges for producing beta-alanine by microbial fermentation. In this study, a high-yield beta-alanine-producing strain was constructed by combining metabolic engineering, protein engineering, and fed-batch bioprocess optimization strategies. First, an aspartate-alpha-decarboxylase from Bacillus subtilis was introduced in Escherichia coli W3110 to construct an initial beta-alanine-producing strain. Production of beta-alanine was obviously increased to 4.36 g/L via improving the metabolic flux and reducing carbon loss by rerouting fluxes of the central carbon metabolism. To further increase beta-alanine production, mechanism-based inactivation of aspartate-a-decarboxylase was relieved by rational design to maintain the productivity at a high level in beta-alanine fed-batch fermentation. Finally, fed-batch bioprocess optimization strategies were used to improve beta-alanine production to 85.18 g/L with 0.24 g/g glucose yield and 1.05 g/L/h productivity in fed-batch fermentation. These strategies can be effectively used in the construction of engineered strains for beta-alanine and production of its derivatives, and the final engineered strain was a valuable microbial cell factory that can be used for the industrial production of beta-alanine.

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