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AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus
As a novel chemical production platform, controllable and inducible modules in Synechococcus elongatus plus the ability of working in diurnal conditions are necessary. To the endeavors, inducible promoters, such as P(Trc), have been refined from Escherichia coli, but the inducer isopropyl-β-D-thioga...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741739/ https://www.ncbi.nlm.nih.gov/pubmed/29273782 http://dx.doi.org/10.1038/s41598-017-17035-4 |
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author | Cao, Yi-Qi Li, Qian Xia, Peng-Fei Wei, Liu-Jing Guo, Ning Li, Jian-Wei Wang, Shu-Guang |
author_facet | Cao, Yi-Qi Li, Qian Xia, Peng-Fei Wei, Liu-Jing Guo, Ning Li, Jian-Wei Wang, Shu-Guang |
author_sort | Cao, Yi-Qi |
collection | PubMed |
description | As a novel chemical production platform, controllable and inducible modules in Synechococcus elongatus plus the ability of working in diurnal conditions are necessary. To the endeavors, inducible promoters, such as P(Trc), have been refined from Escherichia coli, but the inducer isopropyl-β-D-thiogalactoside may cause several side-effects. Meanwhile, to promote the efficiency, photomixotrophic cultivation has been applied in S. elongatus with the additional organic carbon sources. In this study, we developed L-arabinose based modules consisted of both the P(BAD) inducible promoter and the metabolism of L-arabinose in S. elongatus, since L-arabinose is an ideal heterologous feedstock for its availability and economic and environmental benefits. As expected, we achieved homogeneous and linear expression of the exogenous reporter through the P(BAD) promoter, and the biomass increased in diurnal light condition via introducing L-arabinose metabolism pathway. Moreover, the combined AraBAD based toolkit containing both the P(BAD) inducible module and the L-arabinose metabolism module could obtain gene expression and metabolic robustness improvement in S. elongatus. With the only additive L-arabinose, the novel strategy may generate a win-win scenario for both regulation and metabolism for autotrophic bio-production platforms. |
format | Online Article Text |
id | pubmed-5741739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57417392018-01-03 AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus Cao, Yi-Qi Li, Qian Xia, Peng-Fei Wei, Liu-Jing Guo, Ning Li, Jian-Wei Wang, Shu-Guang Sci Rep Article As a novel chemical production platform, controllable and inducible modules in Synechococcus elongatus plus the ability of working in diurnal conditions are necessary. To the endeavors, inducible promoters, such as P(Trc), have been refined from Escherichia coli, but the inducer isopropyl-β-D-thiogalactoside may cause several side-effects. Meanwhile, to promote the efficiency, photomixotrophic cultivation has been applied in S. elongatus with the additional organic carbon sources. In this study, we developed L-arabinose based modules consisted of both the P(BAD) inducible promoter and the metabolism of L-arabinose in S. elongatus, since L-arabinose is an ideal heterologous feedstock for its availability and economic and environmental benefits. As expected, we achieved homogeneous and linear expression of the exogenous reporter through the P(BAD) promoter, and the biomass increased in diurnal light condition via introducing L-arabinose metabolism pathway. Moreover, the combined AraBAD based toolkit containing both the P(BAD) inducible module and the L-arabinose metabolism module could obtain gene expression and metabolic robustness improvement in S. elongatus. With the only additive L-arabinose, the novel strategy may generate a win-win scenario for both regulation and metabolism for autotrophic bio-production platforms. Nature Publishing Group UK 2017-12-22 /pmc/articles/PMC5741739/ /pubmed/29273782 http://dx.doi.org/10.1038/s41598-017-17035-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cao, Yi-Qi Li, Qian Xia, Peng-Fei Wei, Liu-Jing Guo, Ning Li, Jian-Wei Wang, Shu-Guang AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus |
title | AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus |
title_full | AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus |
title_fullStr | AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus |
title_full_unstemmed | AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus |
title_short | AraBAD Based Toolkit for Gene Expression and Metabolic Robustness Improvement in Synechococcus elongatus |
title_sort | arabad based toolkit for gene expression and metabolic robustness improvement in synechococcus elongatus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741739/ https://www.ncbi.nlm.nih.gov/pubmed/29273782 http://dx.doi.org/10.1038/s41598-017-17035-4 |
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