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Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications
The phosphoenolpyruvate-dependent glucose-specific phosphotransferase system (PTS(Glc)) is the main glucose uptake pathway in Escherichia coli that affects both substrate assimilation and metabolism leading to the product formation. In this study, the effect of single PTS(Glc) mutation on cell growt...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541071/ https://www.ncbi.nlm.nih.gov/pubmed/26285685 http://dx.doi.org/10.1038/srep13200 |
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author | Liang, Quanfeng Zhang, Fengyu Li, Yikui Zhang, Xu Li, Jiaojiao Yang, Peng Qi, Qingsheng |
author_facet | Liang, Quanfeng Zhang, Fengyu Li, Yikui Zhang, Xu Li, Jiaojiao Yang, Peng Qi, Qingsheng |
author_sort | Liang, Quanfeng |
collection | PubMed |
description | The phosphoenolpyruvate-dependent glucose-specific phosphotransferase system (PTS(Glc)) is the main glucose uptake pathway in Escherichia coli that affects both substrate assimilation and metabolism leading to the product formation. In this study, the effect of single PTS(Glc) mutation on cell growth and substrate consumption was investigated by knocking out the genes involved in the phosphotransfer cascade of the PTS(Glc). In addition, the distribution of the metabolites of mutants was analyzed. Each mutant was confirmed to have different adaptability in the presence of both glucose and xylose with different ratios, and a substrate mixture with high xylose content can be completely consumed in short time when the ptsI mutant is employed. Finally, ptsH deletion was for the first time applied for succinate production due to its well performance under anaerobic condition. Strain YL104H, in which ptsH was deleted, exhibited considerably increased succinate yield under both aerobic and anaerobic conditions. The succinate titer and overall productivity reached 511.11 mM and 1.01 g/L/h after 60 h during the whole-phase fermentation in a mineral salt medium. The present results demonstrated the glucose and xylose co-utilization efficiency and the product yield and productivity can be significantly improved if a suitable PTS(Glc) deletion mutant was selected. |
format | Online Article Text |
id | pubmed-4541071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45410712015-08-31 Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications Liang, Quanfeng Zhang, Fengyu Li, Yikui Zhang, Xu Li, Jiaojiao Yang, Peng Qi, Qingsheng Sci Rep Article The phosphoenolpyruvate-dependent glucose-specific phosphotransferase system (PTS(Glc)) is the main glucose uptake pathway in Escherichia coli that affects both substrate assimilation and metabolism leading to the product formation. In this study, the effect of single PTS(Glc) mutation on cell growth and substrate consumption was investigated by knocking out the genes involved in the phosphotransfer cascade of the PTS(Glc). In addition, the distribution of the metabolites of mutants was analyzed. Each mutant was confirmed to have different adaptability in the presence of both glucose and xylose with different ratios, and a substrate mixture with high xylose content can be completely consumed in short time when the ptsI mutant is employed. Finally, ptsH deletion was for the first time applied for succinate production due to its well performance under anaerobic condition. Strain YL104H, in which ptsH was deleted, exhibited considerably increased succinate yield under both aerobic and anaerobic conditions. The succinate titer and overall productivity reached 511.11 mM and 1.01 g/L/h after 60 h during the whole-phase fermentation in a mineral salt medium. The present results demonstrated the glucose and xylose co-utilization efficiency and the product yield and productivity can be significantly improved if a suitable PTS(Glc) deletion mutant was selected. Nature Publishing Group 2015-08-19 /pmc/articles/PMC4541071/ /pubmed/26285685 http://dx.doi.org/10.1038/srep13200 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Liang, Quanfeng Zhang, Fengyu Li, Yikui Zhang, Xu Li, Jiaojiao Yang, Peng Qi, Qingsheng Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications |
title | Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications |
title_full | Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications |
title_fullStr | Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications |
title_full_unstemmed | Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications |
title_short | Comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications |
title_sort | comparison of individual component deletions in a glucose-specific phosphotransferase system revealed their different applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541071/ https://www.ncbi.nlm.nih.gov/pubmed/26285685 http://dx.doi.org/10.1038/srep13200 |
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