Journal
BIOTECHNOLOGY PROGRESS
Volume 37, Issue 1, Pages -Publisher
WILEY
DOI: 10.1002/btpr.3072
Keywords
2; 3-butanediol; Bacillus licheniformis; CRISPR-Cas9; fermentation; selectivity
Funding
- Biochemical Industry Promoting Technology Development Project [10050407]
- Ministry of Trade, Industry and Energy (MOTIE, Korea)
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This study successfully used the CRISPR-Cas9 system to engineer the B. licheniformis strain, demonstrating efficient gene deletion, sequential gene deletion, and the potential for producing (2R,3S)-BDO. The research also confirmed the stereospecific production of (2R,3S)-BDO with a deletion mutant, showing promising results for industrial applications.
Bacillus lichenformisis an industrially promising generally recognized as safe (GRAS) strain that can be used for the production of a valuable chemical, 2,3-butanediol (BDO). Conventional gene deletion vectors and/or methods are time-consuming and have poor efficiency. Therefore, clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 mediated homologous recombination was used to engineer a newly isolated and UV-mutagenizedB. licheniformis4071-15 strain. With the help of a CRISPR-Cas9 system, this one-step process could be used for the deletion ofldhgene within 4 days with high-efficiency exceeding 60%. In addition, the sequential deletion of target genes for engineering studies was evaluated, and it was confirmed that a triple mutant strain (ldh,dgp, andacoR) could be obtained by repeated one-step cycles. Furthermore, a practical metabolic engineering study was carried out using a CRISPR-Cas9 system for the stereospecific production of (2R,3S)-BDO. The predicted (2R,3R)-butanediol dehydrogenase encoded by thegdhgene was selected as a target for the production of (2R,3S)-BDO, and the mutant was successfully obtained. The results show that the stereospecific production of (2R,3S)-BDO was possible with thegdhdeletion mutant, while the 4071-15 host strain still generated 26% of (2R,3R)-BDO. It was also shown that the 4071-15 Delta gdhmutant could produce 115 g/L of (2R,3S)-BDO in 64 hr by two-stage fed-batch fermentation. This study has shown the efficient development of a (2R,3S)-BDO producingB. licheniformisstrain based on CRISPR-Cas9 and fermentation technologies.
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