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

被引:78
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
BIOTECHNOLOGY FOR BIOFUELS | 2016年 / 9卷
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.
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页数:14
相关论文
共 57 条
  • [1] Regulation of the NADH pool and NADH/NADPH ratio redistributes acetoin and 2,3-butanediol proportion in Bacillus subtilis
    Bao, Teng
    Zhang, Xian
    Zhao, Xiaojing
    Rao, Zhiming
    Yang, Taowei
    Yang, Shangtian
    [J]. BIOTECHNOLOGY JOURNAL, 2015, 10 (08) : 1298 - 1306
  • [2] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [3] Overexpression and biochemical characterization of soluble pyridine nucleotide transhydrogenase from Escherichia coli
    Cao, Zhengyu
    Song, Ping
    Xu, Qin
    Su, Ruirui
    Zhu, Guoping
    [J]. FEMS MICROBIOLOGY LETTERS, 2011, 320 (01) : 9 - 14
  • [4] Biotechnological production of 2,3-butanediol-Current state and prospects
    Celinska, E.
    Grajek, W.
    [J]. BIOTECHNOLOGY ADVANCES, 2009, 27 (06) : 715 - 725
  • [5] Engineering Bacillus subtilis for acetoin production from glucose and xylose mixtures
    Chen, Tao
    Liu, Wei-xi
    Fu, Jing
    Zhang, Bo
    Tang, Ya-jie
    [J]. JOURNAL OF BIOTECHNOLOGY, 2013, 168 (04) : 499 - 505
  • [6] The LysR-type transcriptional regulator (LTTR) AlsR indirectly regulates expression of the Bacillus subtilis bdhA gene encoding 2,3-butanediol dehydrogenase
    de Oliveira, Rafael R.
    Nicholson, Wayne L.
    [J]. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2013, 97 (16) : 7307 - 7316
  • [7] THE BACILLUS-SUBTILIS-SIGL GENE ENCODES AN EQUIVALENT OF SIGMA-54 FROM GRAM-NEGATIVE BACTERIA
    DEBARBOUILLE, M
    MARTINVERSTRAETE, I
    KUNST, F
    RAPOPORT, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (20) : 9092 - 9096
  • [8] A new mutation delivery system for genome-scale approaches in Bacillus subtilis
    Fabret, C
    Ehrlich, SD
    Noirot, P
    [J]. MOLECULAR MICROBIOLOGY, 2002, 46 (01) : 25 - 36
  • [9] The Transcription Factor AlsR Binds and Regulates the Promoter of the alsSD Operon Responsible for Acetoin Formation in Bacillus subtilis
    Fraedrich, Claudia
    March, Anika
    Fiege, Kerstin
    Hartmann, Anja
    Jahn, Dieter
    Haertig, Elisabeth
    [J]. JOURNAL OF BACTERIOLOGY, 2012, 194 (05) : 1100 - 1112
  • [10] NADH Plays the Vital Role for Chiral Pure D-(-)-2,3-Butanediol Production in Bacillus subtilis Under Limited Oxygen Conditions
    Fu, Jing
    Wang, Zhiwen
    Chen, Tao
    Liu, Weixi
    Shi, Ting
    Wang, Guanglu
    Tang, Ya-jie
    Zhao, Xueming
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2014, 111 (10) : 2126 - 2131