» Articles » PMID: 37334270

Study on the Construction Technology of β-alanine Synthesizing Based on Cellulosome Assembly

Overview
Date 2023 Jun 19
PMID 37334270
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

One-Pot Synthesis of β-Alanine from Fumaric Acid via an Efficient Dual-Enzyme Cascade Biotransformation.

Ni Z, Zhang L, Nie A, Wang H, Wu X Biomolecules. 2025; 14(12.

PMID: 39766260 PMC: 11674828. DOI: 10.3390/biom14121553.

References
1.
Piao X, Wang L, Lin B, Chen H, Liu W, Tao Y . Metabolic engineering of Escherichia coli for production of L-aspartate and its derivative β-alanine with high stoichiometric yield. Metab Eng. 2019; 54:244-254. DOI: 10.1016/j.ymben.2019.04.012. View

2.
Pandurangan M, Enkhtaivan G, Mistry B, Patel R, Moon S, Kim D . β-Alanine intercede metabolic recovery for amelioration of human cervical and renal tumors. Amino Acids. 2017; 49(8):1373-1380. DOI: 10.1007/s00726-017-2437-y. View

3.
Wang J, Rao Z, Xu J, Zhang W . Enhancing β-alanine production from glucose in genetically modified Corynebacterium glutamicum by metabolic pathway engineering. Appl Microbiol Biotechnol. 2021; 105(24):9153-9166. DOI: 10.1007/s00253-021-11696-y. View

4.
Xiao J, Wang Q, Xiao K, Zhu W, Huang J, Cai X . Generation of markerless and multiple-gene knockout in Glaesserella parasuis based on natural transformation and Flp recombinase. Appl Microbiol Biotechnol. 2022; 106(13-16):5167-5178. DOI: 10.1007/s00253-022-11994-z. View

5.
Yu X, Huang C, Xu X, Chen H, Liang M, Xu Z . Protein Engineering of a Pyridoxal-5'-Phosphate-Dependent l-Aspartate-α-Decarboxylase from for β-Alanine Production. Molecules. 2020; 25(6). PMC: 7143960. DOI: 10.3390/molecules25061280. View