β-Alanine is the only β-amino acid in nature; it is widely used in food additives, medicines, health products, and surfactants. To avoid pollution caused by traditional production methods, the synthesis of β-alanine has been gradually replaced by microbial fermentation and enzyme catalysis, which is a green, mild, and high-yield biosynthesis method. In this study, we constructed an recombinant strain for efficient β-alanine production using glucose as the raw material. The microbial synthesis pathway of L-lysine-producing strain, CGMCC 1.366, was modified using gene editing by knocking out the aspartate kinase gene, . The catalytic efficiency and product synthesis efficiency were improved by assembling key enzymes with cellulosome. By-product accumulation was reduced by blocking the L-lysine production pathway, thereby increasing the yield of β-alanine. In addition, catalytic efficiency was improved by the two-enzyme method to further increase the β-alanine content. The key cellulosome elements, dockerin () and cohesin (), were combined with L-aspartate-α-decarboxylase () from and aspartate aminotransferase () from to improve the catalytic efficiency and expression level of the enzyme. β-alanine production reached 7.439 mg/L and 25.87 mg/L in the two engineered strains. The β-alanine content reached 755.465 mg/L in a 5 L fermenter. The content of β-alanine synthesized by constructed β-alanine engineering strains were 10.47 times and 36.42 times higher than the engineered strain without assembled cellulosomes, respectively. This research lays the foundation for the enzymatic production of β-alanine using a cellulosome multi-enzyme self-assembly system.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273014PMC
http://dx.doi.org/10.3389/fbioe.2023.1202483DOI Listing

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