Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production

被引:77
|
作者
Fu, Jing [1 ]
Huo, Guangxin [1 ]
Feng, Lili [1 ]
Mao, Yufeng [1 ]
Wang, Zhiwen [1 ]
Ma, Hongwu [3 ]
Chen, Tao [1 ,2 ]
Zhao, Xueming [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Key Lab Syst Bioengn,Minist Educ,SynBio Res Platf, Tianjin 300072, Peoples R China
[2] Hubei Univ Technol, Hubei Prov Cooperat Innovat Ctr Ind Fermentat, Key Lab Fermentat Engn, Minist Educ, Wuhan 430068, Peoples R China
[3] Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Key Lab Syst Microbial Biotechnol, Tianjin 300308, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Metabolic engineering; Meso-2,3-butanediol; D-(-)-2,3-butanediol; Bacillus subtilis; Cofactor engineering; ENHANCED 2,3-BUTANEDIOL PRODUCTION; BIODIESEL-DERIVED GLYCEROL; SACCHAROMYCES-CEREVISIAE; KLEBSIELLA-PNEUMONIAE; ESCHERICHIA-COLI; GENE-EXPRESSION; ACETOIN; DEHYDROGENASE; STRAIN; OXYGEN;
D O I
10.1186/s13068-016-0502-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: 2,3-Butanediol (2,3-BD) with low toxicity to microbes, could be a promising alternative for biofuel production. However, most of the 2,3-BD producers are opportunistic pathogens that are not suitable for industrialscale fermentation. In our previous study, wild-type Bacillus subtilis 168, as a class I microorganism, was first found to generate only D-(-)-2,3-BD (purity > 99 %) under low oxygen conditions. Results: In this work, B. subtilis was engineered to produce chiral pure meso-2,3-BD. First, d-(-)-2,3-BD production was abolished by deleting d-(-)-2,3-BD dehydrogenase coding gene bdhA, and acoA gene was knocked out to prevent the degradation of acetoin (AC), the immediate precursor of 2,3-BD. Next, both pta and ldh gene were deleted to decrease the accumulation of the byproducts, acetate and l-lactate. We further introduced the meso-2,3-BD dehydrogenase coding gene budC from Klebsiella pneumoniae CICC10011, as well as overexpressed alsSD in the tetra-mutant (Delta acoA Delta bdhA Delta pta Delta ldh) to achieve the efficient production of chiral meso-2,3-BD. Finally, the pool of NADH availability was further increased to facilitate the conversion of meso-2,3-BD from AC by overexpressing udhA gene (coding a soluble transhydrogenase) and low dissolved oxygen control during the cultivation. Under microaerobic oxygen conditions, the best strain BSF9 produced 103.7 g/L meso-2,3-BD with a yield of 0.487 g/g glucose in the 5-L batch fermenter, and the titer of the main byproduct AC was no more than 1.1 g/L. Conclusion: This work offered a novel strategy for the production of chiral pure meso-2,3-BD in B. subtilis. To our knowledge, this is the first report indicating that metabolic engineered B. subtilis could produce chiral meso-2,3-BD with high purity under limited oxygen conditions. These results further demonstrated that B. subtilis as a class I microorganism is a competitive industrial-level meso-2,3-BD producer.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production
    Jing Fu
    Guangxin Huo
    Lili Feng
    Yufeng Mao
    Zhiwen Wang
    Hongwu Ma
    Tao Chen
    Xueming Zhao
    Biotechnology for Biofuels, 9
  • [2] Engineering Bacillus licheniformis for the production of meso-2,3-butanediol
    Yimin Qiu
    Jinyan Zhang
    Lu Li
    Zhiyou Wen
    Christopher T. Nomura
    Shuilin Wu
    Shouwen Chen
    Biotechnology for Biofuels, 9
  • [3] Engineering Bacillus licheniformis for the production of meso-2,3-butanediol
    Qiu, Yimin
    Zhang, Jinyan
    Li, Lu
    Wen, Zhiyou
    Nomura, Christopher T.
    Wu, Shuilin
    Chen, Shouwen
    BIOTECHNOLOGY FOR BIOFUELS, 2016, 9
  • [4] Metabolic engineering of thermophilic Bacillus licheniformis for chiral pure D-2,3-butanediol production
    Wang, Qingzhao
    Chen, Tao
    Zhao, Xueming
    Chamu, Jauhleene
    BIOTECHNOLOGY AND BIOENGINEERING, 2012, 109 (07) : 1610 - 1621
  • [5] Biochemical characterization of unusual meso-2,3-butanediol dehydrogenase from a strain of Bacillus subtilis
    Hao, Wenbo
    Ji, Fangling
    Wang, Jingyun
    Zhang, Yue
    Wang, Tianqi
    Bao, Yongming
    JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 2014, 109 : 184 - 190
  • [6] Deletion of meso-2,3-butanediol dehydrogenase gene budC for enhanced D-2,3-butanediol production in Bacillus licheniformis
    Qi, Gaofu
    Kang, Yanfang
    Li, Lu
    Xiao, Aifang
    Zhang, Shumeng
    Wen, Zhiyou
    Xu, Dihong
    Chen, Shouwen
    BIOTECHNOLOGY FOR BIOFUELS, 2014, 7
  • [7] Metabolic engineering of acetoin and meso-2,3-butanediol biosynthesis in E. coli
    Nielsen, David R.
    Yoon, Sang-Hwal
    Yuan, Clara J.
    Prather, Kristala L. J.
    BIOTECHNOLOGY JOURNAL, 2010, 5 (03) : 274 - 284
  • [8] Deletion of meso-2,3-butanediol dehydrogenase gene bud C for enhanced D-2,3-butanediol production in Bacillus licheniformis
    Gaofu Qi
    Yanfang Kang
    Lu Li
    Aifang Xiao
    Shumeng Zhang
    Zhiyou Wen
    Dihong Xu
    Shouwen Chen
    Biotechnology for Biofuels, 7
  • [9] Metabolic engineering of the marine bacteria Neptunomonas concharum for the production of acetoin and meso-2,3-butanediol from acetate
    Li, Wei
    Pu, Nan
    Liu, Chang-Xia
    Yuan, Qi-Peng
    Li, Zheng-Jun
    BIOCHEMICAL ENGINEERING JOURNAL, 2019, 151
  • [10] PRODUCTION AND PROPERTIES OF 2,3-BUTANEDIOL .24. THE CYCLIC SULPHITES OF MESO-2,3-BUTANEDIOL AND LEVO-2,3-BUTANEDIOL
    ROBERTSON, FM
    NEISH, AC
    CANADIAN JOURNAL OF RESEARCH SECTION B-CHEMICAL SCIENCES, 1947, 25 (06): : 491 - 493