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

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 industrial-scale fermentation. In our previous study, wild-type Bacillus subtilis 16...

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Autores principales: Fu, Jing, Huo, Guangxin, Feng, Lili, Mao, Yufeng, Wang, Zhiwen, Ma, Hongwu, Chen, Tao, Zhao, Xueming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837526/
https://www.ncbi.nlm.nih.gov/pubmed/27099629
http://dx.doi.org/10.1186/s13068-016-0502-5
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author Fu, Jing
Huo, Guangxin
Feng, Lili
Mao, Yufeng
Wang, Zhiwen
Ma, Hongwu
Chen, Tao
Zhao, Xueming
author_facet Fu, Jing
Huo, Guangxin
Feng, Lili
Mao, Yufeng
Wang, Zhiwen
Ma, Hongwu
Chen, Tao
Zhao, Xueming
author_sort Fu, Jing
collection PubMed
description 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 industrial-scale 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 Klebsiellapneumoniae CICC10011, as well as overexpressed alsSD in the tetra-mutant (ΔacoAΔbdhAΔptaΔldh) 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0502-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-48375262016-04-21 Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production Fu, Jing Huo, Guangxin Feng, Lili Mao, Yufeng Wang, Zhiwen Ma, Hongwu Chen, Tao Zhao, Xueming Biotechnol Biofuels Research 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 industrial-scale 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 Klebsiellapneumoniae CICC10011, as well as overexpressed alsSD in the tetra-mutant (ΔacoAΔbdhAΔptaΔldh) 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0502-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-19 /pmc/articles/PMC4837526/ /pubmed/27099629 http://dx.doi.org/10.1186/s13068-016-0502-5 Text en © Fu et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Fu, Jing
Huo, Guangxin
Feng, Lili
Mao, Yufeng
Wang, Zhiwen
Ma, Hongwu
Chen, Tao
Zhao, Xueming
Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production
title Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production
title_full Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production
title_fullStr Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production
title_full_unstemmed Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production
title_short Metabolic engineering of Bacillus subtilis for chiral pure meso-2,3-butanediol production
title_sort metabolic engineering of bacillus subtilis for chiral pure meso-2,3-butanediol production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837526/
https://www.ncbi.nlm.nih.gov/pubmed/27099629
http://dx.doi.org/10.1186/s13068-016-0502-5
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