Abstract
Glutaric acid is an important organic acid applied widely in different fields. Most previous researches have focused on the production of glutaric acid in various strains using the 5-aminovaleric acid (AMV) or pentenoic acid synthesis pathways. We previously utilized a five-step reversed adipic acid degradation pathway (RADP) in Escherichia coli BL21 (DE3) to construct strain Bgl146. Herein, we found that malonyl-CoA was strictly limited in this strain, and increasing its abundance could improve glutaric acid production. We, therefore, constructed a malonic acid uptake pathway in E. coli using matB (malonic acid synthetase) and matC (malonic acid carrier protein) from Clover rhizobia. The titer of glutaric acid was improved by 2.1-fold and 1.45-fold, respectively, reaching 0.56 g/L and 4.35 g/L in shake flask and batch fermentation following addition of malonic acid. Finally, the highest titer of glutaric acid was 6.3 g/L in fed-batch fermentation at optimized fermentation conditions.
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Acknowledgements
This work was supported by the National Key R&D Program of China (2018YFA0901400), the National Natural Science Foundation of China (21877053, 31600044), the Open Project Program of China–Canada Joint Lab of Food Nutrition and Health, Beijing Technology and Business University (BTBU), and the Fundamental Research Funds for the Central Universities (JUSRP51705A, JUSRP11964).
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Sui, X., Zhao, M., Liu, Y. et al. Enhancing glutaric acid production in Escherichia coli by uptake of malonic acid. J Ind Microbiol Biotechnol 47, 311–318 (2020). https://doi.org/10.1007/s10295-020-02268-6
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DOI: https://doi.org/10.1007/s10295-020-02268-6