The production of coenzyme B using well-characterized microorganisms, such as Escherichia coli, has recently attracted considerable attention to meet growing demands of coenzyme B in various applications. In the present study, we designed an auxotrophic selection strategy and demonstrated the enhanced production of coenzyme B using a previously engineered coenzyme B-producing E. coli strain. To select a high producer, the coenzyme B-independent methionine synthase (metE) gene was deleted in E. coli, thus limiting its methionine synthesis to only that via coenzyme B-dependent synthase (encoded by metH). Following the deletion of metE, significantly enhanced production of the specific coenzyme B validated the coenzyme B-dependent auxotrophic growth. Further precise tuning of the auxotrophic system by varying the expression of metH substantially increased the cell biomass and coenzyme B production, suggesting that our strategy could be effectively applied to E. coli and other coenzyme B-producing strains.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033360 | PMC |
http://dx.doi.org/10.1016/j.isci.2020.100890 | DOI Listing |
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