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Enhanced 2,3-Butanediol Production in Recombinant Klebsiella pneumoniae via Overexpression of Synthesis-Related Genes

Authors
Kim, BorimLee, SoojinPark, JoohongLu, MingshouOh, MinkyuKim, YoungrokLee, Jinwon
Issue Date
Sep-2012
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
Keywords
2,3-Butanediol; Klebsiella pneumoniae; gene manipulation; acetolactate decarboxylase; acetolactate synthase; alcohol dehydrogenase
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.22, no.9, pp.1258 - 1263
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume
22
Number
9
Start Page
1258
End Page
1263
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/107600
DOI
10.4014/jmb.1201.01044
ISSN
1017-7825
Abstract
2,3-Butanediol (2,3-BD) is a major metabolite produced by Klebsiella pneumoniae KCTC2242, which is a important chemical with wide applications. Three genes important for 2,3-BD biosynthesis acetolactate decarboxylase (budA), acetolactate synthase (budB), and alcohol dehydrogenase (budC) were identified in K. pneumoniae genomic DNA. With the goal of enhancing 2,3-BD production, these genes were cloned into pUC18K expression vectors containing the lacZ promoter and the kanamycin resistance gene to generate plasmids pSB1-7. The plasmids were then introduced into K. pneumoniae using electroporation. All strains were incubated in flask experiments and 2,3-BD production was increased by 60% in recombinant bacteria harboring pSB04 (budA and budB genes), compared with the parental strain K. pneumoniae KCTC2242. The maximum 2,3-BD production level achieved through fed-batch fermentation with K. pneumoniae SGJSB04 was 101.53 g/l over 40 h with a productivity of 2.54 g/l.h. These results suggest that overexpression of 2,3-BD synthesis-related genes can enhance 2,3-BD production in K. pneumoniae by fermentation.
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