Department of Chemical and Biomolecular Engineering, Sogang University, Seoul, Korea.
J Microbiol Biotechnol. 2012 Sep;22(9):1258-63. doi: 10.4014/jmb.1201.01044.
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 fedbatch 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 synthesisrelated genes can enhance 2,3-BD production in K. pneumoniae by fermentation.
2,3-丁二醇(2,3-BD)是肺炎克雷伯氏菌 KCTC2242 产生的一种主要代谢产物,是一种具有广泛应用的重要化学品。在肺炎克雷伯氏菌基因组 DNA 中鉴定出了三个对 2,3-BD 生物合成至关重要的基因:乙酰乳酸脱羧酶(budA)、乙酰乳酸合酶(budB)和醇脱氢酶(budC)。为了提高 2,3-BD 的产量,这些基因被克隆到含有 lacZ 启动子和卡那霉素抗性基因的 pUC18K 表达载体中,生成质粒 pSB1-7。然后通过电穿孔将质粒引入肺炎克雷伯氏菌中。所有菌株均在摇瓶实验中孵育,与原始菌株肺炎克雷伯氏菌 KCTC2242 相比,携带 pSB04(budA 和 budB 基因)的重组菌的 2,3-BD 产量提高了 60%。通过肺炎克雷伯氏菌 SGJSB04 的分批补料发酵,最大 2,3-BD 产量达到 101.53 g/l,生产率为 2.54 g/l.h。这些结果表明,通过发酵过表达 2,3-BD 合成相关基因可以提高肺炎克雷伯氏菌中的 2,3-BD 产量。