2015
DOI: 10.1016/j.jbiotec.2015.06.385
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A non-pathogenic and optically high concentrated (R,R)-2,3-butanediol biosynthesizing Klebsiella strain

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Cited by 12 publications
(3 citation statements)
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“…To increase the final 2,3-butanediol concentration, additional glucose supplementation during the cultivation is essential [10, 15]. Additionally, genetic engineering to decrease by-product formation and to enable production of optically pure 2,3-butanediol will be beneficial [12, 51, 52]. Furthermore, the cultivation medium has to be optimized with respect to utilization of cheaper carbon sources and media components [18, 23, 30, 53, 54].…”
Section: Discussionmentioning
confidence: 99%
“…To increase the final 2,3-butanediol concentration, additional glucose supplementation during the cultivation is essential [10, 15]. Additionally, genetic engineering to decrease by-product formation and to enable production of optically pure 2,3-butanediol will be beneficial [12, 51, 52]. Furthermore, the cultivation medium has to be optimized with respect to utilization of cheaper carbon sources and media components [18, 23, 30, 53, 54].…”
Section: Discussionmentioning
confidence: 99%
“…The NADH availability and the carbon flux towards BDO production were enhanced leading to BDO conversion yield of 0.46 g g -1 . Lee et al (2015) developed a mutant K. pneumoniae strain by deleting the protein secreting outer core polysaccharides. Further, overexpression of the glycerol dehydrogenase gene (gldA and dhaD) and deletion of ldhA enhanced the production of D-BDO to 61 g L -1 in a fed-batch cultivation strategy using glycerol as carbon source.…”
Section: Klebsiella Spmentioning
confidence: 99%
“…Optically pure (2R,3R)-BDO can be produced by knocking out the endogenous gene encoding (2R,3S)-BDO dehydrogenase and thus preventing (2R,3S)-BDO formation. Using this strategy, various recombinant strains including K. pneumonia, [84] S. marcescens, [85] Enterobacter cloacae, [86] and Bacillus licheniformis [87,88] have been developed for the production of (2R,3R)-BDO. Alternatively, budC was deleted in recombinant K. oxytoca strain with disruption of ldhA and pflB genes by integration of the Paenibacillus polymyxa bdh gene.…”
Section: -Butanolmentioning
confidence: 99%