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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-4837526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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