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.
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页数:14
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