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Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism
Central carbon metabolism is a basic and exhaustively analyzed pathway. However, the intrinsic robustness of the pathway might still conceal uncharacterized reactions. To test this hypothesis, we constructed systematic multiple-knockout mutants involved in central carbon catabolism in Escherichia co...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758719/ https://www.ncbi.nlm.nih.gov/pubmed/19756045 http://dx.doi.org/10.1038/msb.2009.65 |
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author | Nakahigashi, Kenji Toya, Yoshihiro Ishii, Nobuyoshi Soga, Tomoyoshi Hasegawa, Miki Watanabe, Hisami Takai, Yuki Honma, Masayuki Mori, Hirotada Tomita, Masaru |
author_facet | Nakahigashi, Kenji Toya, Yoshihiro Ishii, Nobuyoshi Soga, Tomoyoshi Hasegawa, Miki Watanabe, Hisami Takai, Yuki Honma, Masayuki Mori, Hirotada Tomita, Masaru |
author_sort | Nakahigashi, Kenji |
collection | PubMed |
description | Central carbon metabolism is a basic and exhaustively analyzed pathway. However, the intrinsic robustness of the pathway might still conceal uncharacterized reactions. To test this hypothesis, we constructed systematic multiple-knockout mutants involved in central carbon catabolism in Escherichia coli and tested their growth under 12 different nutrient conditions. Differences between in silico predictions and experimental growth indicated that unreported reactions existed within this extensively analyzed metabolic network. These putative reactions were then confirmed by metabolome analysis and in vitro enzymatic assays. Novel reactions regarding the breakdown of sedoheptulose-7-phosphate to erythrose-4-phosphate and dihydroxyacetone phosphate were observed in transaldolase-deficient mutants, without any noticeable changes in gene expression. These reactions, triggered by an accumulation of sedoheptulose-7-phosphate, were catalyzed by the universally conserved glycolytic enzymes ATP-dependent phosphofructokinase and aldolase. The emergence of an alternative pathway not requiring any changes in gene expression, but rather relying on the accumulation of an intermediate metabolite may be a novel mechanism mediating the robustness of these metabolic networks. |
format | Text |
id | pubmed-2758719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27587192009-10-09 Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism Nakahigashi, Kenji Toya, Yoshihiro Ishii, Nobuyoshi Soga, Tomoyoshi Hasegawa, Miki Watanabe, Hisami Takai, Yuki Honma, Masayuki Mori, Hirotada Tomita, Masaru Mol Syst Biol Article Central carbon metabolism is a basic and exhaustively analyzed pathway. However, the intrinsic robustness of the pathway might still conceal uncharacterized reactions. To test this hypothesis, we constructed systematic multiple-knockout mutants involved in central carbon catabolism in Escherichia coli and tested their growth under 12 different nutrient conditions. Differences between in silico predictions and experimental growth indicated that unreported reactions existed within this extensively analyzed metabolic network. These putative reactions were then confirmed by metabolome analysis and in vitro enzymatic assays. Novel reactions regarding the breakdown of sedoheptulose-7-phosphate to erythrose-4-phosphate and dihydroxyacetone phosphate were observed in transaldolase-deficient mutants, without any noticeable changes in gene expression. These reactions, triggered by an accumulation of sedoheptulose-7-phosphate, were catalyzed by the universally conserved glycolytic enzymes ATP-dependent phosphofructokinase and aldolase. The emergence of an alternative pathway not requiring any changes in gene expression, but rather relying on the accumulation of an intermediate metabolite may be a novel mechanism mediating the robustness of these metabolic networks. Nature Publishing Group 2009-09-15 /pmc/articles/PMC2758719/ /pubmed/19756045 http://dx.doi.org/10.1038/msb.2009.65 Text en Copyright © 2009, EMBO and Nature Publishing Group http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits distribution and reproduction in any medium, provided the original author and source are credited. Creation of derivative works is permitted but the resulting work may be distributed only under the same or similar licence to this one. This licence does not permit commercial exploitation without specific permission. |
spellingShingle | Article Nakahigashi, Kenji Toya, Yoshihiro Ishii, Nobuyoshi Soga, Tomoyoshi Hasegawa, Miki Watanabe, Hisami Takai, Yuki Honma, Masayuki Mori, Hirotada Tomita, Masaru Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism |
title | Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism |
title_full | Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism |
title_fullStr | Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism |
title_full_unstemmed | Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism |
title_short | Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism |
title_sort | systematic phenome analysis of escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758719/ https://www.ncbi.nlm.nih.gov/pubmed/19756045 http://dx.doi.org/10.1038/msb.2009.65 |
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