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Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine
BACKGROUND: Genome streamlining has emerged as an effective strategy to boost the production efficiency of bio-based products. Many efforts have been made to construct desirable chassis cells by reducing the genome size of microbes. It has been reported that the genome-reduced Bacillus subtilis stra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893254/ https://www.ncbi.nlm.nih.gov/pubmed/27260256 http://dx.doi.org/10.1186/s12934-016-0494-7 |
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author | Li, Yang Zhu, Xujun Zhang, Xueyu Fu, Jing Wang, Zhiwen Chen, Tao Zhao, Xueming |
author_facet | Li, Yang Zhu, Xujun Zhang, Xueyu Fu, Jing Wang, Zhiwen Chen, Tao Zhao, Xueming |
author_sort | Li, Yang |
collection | PubMed |
description | BACKGROUND: Genome streamlining has emerged as an effective strategy to boost the production efficiency of bio-based products. Many efforts have been made to construct desirable chassis cells by reducing the genome size of microbes. It has been reported that the genome-reduced Bacillus subtilis strain MBG874 showed clear advantages for the production of several heterologous enzymes including alkaline cellulase and protease. In addition to enzymes, B. subtilis is also used for the production of chemicals. To our best knowledge, it is still unknown whether genome reduction could be used to optimize the production of chemicals such as nucleoside products. RESULTS: In this study, we constructed a series of genome-reduced strains by deleting non-essential regions in the chromosome of B. subtilis 168. These strains with genome reductions ranging in size from 581.9 to 814.4 kb displayed markedly decreased growth rates, sporulation ratios, transformation efficiencies and maintenance coefficients, as well as increased cell yields. We re-engineered the genome-reduced strains to produce guanosine and thymidine, respectively. The strain BSK814G2, in which purA was knocked out, and prs, purF and guaB were co-overexpressed, produced 115.2 mg/L of guanosine, which was 4.4-fold higher compared to the control strain constructed by introducing the same gene modifications into the parental strain. We also constructed a thymidine producer by deleting the tdk gene and overexpressing the prs, ushA, thyA, dut, and ndk genes from Escherichia coli in strain BSK756, and the resulting strain BSK756T3 accumulated 151.2 mg/L thymidine, showing a 5.2-fold increase compared to the corresponding control strain. CONCLUSIONS: Genome-scale genetic manipulation has a variety of effects on the physiological characteristics and cell metabolism of B. subtilis. By introducing specific gene modifications related to guanosine and thymidine accumulation, respectively, we demonstrated that genome-reduced strains had greatly improved properties compared to the wild-type strain as chassis cells for the production of these two products. These strains also have great potential for the production of other nucleosides and similar derived chemicals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0494-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4893254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48932542016-06-05 Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine Li, Yang Zhu, Xujun Zhang, Xueyu Fu, Jing Wang, Zhiwen Chen, Tao Zhao, Xueming Microb Cell Fact Research BACKGROUND: Genome streamlining has emerged as an effective strategy to boost the production efficiency of bio-based products. Many efforts have been made to construct desirable chassis cells by reducing the genome size of microbes. It has been reported that the genome-reduced Bacillus subtilis strain MBG874 showed clear advantages for the production of several heterologous enzymes including alkaline cellulase and protease. In addition to enzymes, B. subtilis is also used for the production of chemicals. To our best knowledge, it is still unknown whether genome reduction could be used to optimize the production of chemicals such as nucleoside products. RESULTS: In this study, we constructed a series of genome-reduced strains by deleting non-essential regions in the chromosome of B. subtilis 168. These strains with genome reductions ranging in size from 581.9 to 814.4 kb displayed markedly decreased growth rates, sporulation ratios, transformation efficiencies and maintenance coefficients, as well as increased cell yields. We re-engineered the genome-reduced strains to produce guanosine and thymidine, respectively. The strain BSK814G2, in which purA was knocked out, and prs, purF and guaB were co-overexpressed, produced 115.2 mg/L of guanosine, which was 4.4-fold higher compared to the control strain constructed by introducing the same gene modifications into the parental strain. We also constructed a thymidine producer by deleting the tdk gene and overexpressing the prs, ushA, thyA, dut, and ndk genes from Escherichia coli in strain BSK756, and the resulting strain BSK756T3 accumulated 151.2 mg/L thymidine, showing a 5.2-fold increase compared to the corresponding control strain. CONCLUSIONS: Genome-scale genetic manipulation has a variety of effects on the physiological characteristics and cell metabolism of B. subtilis. By introducing specific gene modifications related to guanosine and thymidine accumulation, respectively, we demonstrated that genome-reduced strains had greatly improved properties compared to the wild-type strain as chassis cells for the production of these two products. These strains also have great potential for the production of other nucleosides and similar derived chemicals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0494-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-03 /pmc/articles/PMC4893254/ /pubmed/27260256 http://dx.doi.org/10.1186/s12934-016-0494-7 Text en © The Author(s) 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 Li, Yang Zhu, Xujun Zhang, Xueyu Fu, Jing Wang, Zhiwen Chen, Tao Zhao, Xueming Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine |
title | Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine |
title_full | Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine |
title_fullStr | Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine |
title_full_unstemmed | Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine |
title_short | Characterization of genome-reduced Bacillus subtilis strains and their application for the production of guanosine and thymidine |
title_sort | characterization of genome-reduced bacillus subtilis strains and their application for the production of guanosine and thymidine |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893254/ https://www.ncbi.nlm.nih.gov/pubmed/27260256 http://dx.doi.org/10.1186/s12934-016-0494-7 |
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