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XTMS: pathway design in an eXTended metabolic space
As metabolic engineering and synthetic biology progress toward reaching the goal of a more sustainable use of biological resources, the need of increasing the number of value-added chemicals that can be produced in industrial organisms becomes more imperative. Exploring, however, the vast possibilit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086079/ https://www.ncbi.nlm.nih.gov/pubmed/24792156 http://dx.doi.org/10.1093/nar/gku362 |
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author | Carbonell, Pablo Parutto, Pierre Herisson, Joan Pandit, Shashi Bhushan Faulon, Jean-Loup |
author_facet | Carbonell, Pablo Parutto, Pierre Herisson, Joan Pandit, Shashi Bhushan Faulon, Jean-Loup |
author_sort | Carbonell, Pablo |
collection | PubMed |
description | As metabolic engineering and synthetic biology progress toward reaching the goal of a more sustainable use of biological resources, the need of increasing the number of value-added chemicals that can be produced in industrial organisms becomes more imperative. Exploring, however, the vast possibility of pathways amenable to engineering through heterologous genes expression in a chassis organism is complex and unattainable manually. Here, we present XTMS, a web-based pathway analysis platform available at http://xtms.issb.genopole.fr, which provides full access to the set of pathways that can be imported into a chassis organism such as Escherichia coli through the application of an Extended Metabolic Space modeling framework. The XTMS approach consists on determining the set of biochemical transformations that can potentially be processed in vivo as modeled by molecular signatures, a specific coding system for derivation of reaction rules for metabolic reactions and enumeration of all the corresponding substrates and products. Most promising routes are described in terms of metabolite exchange, maximum allowable pathway yield, toxicity and enzyme efficiency. By answering such critical design points, XTMS not only paves the road toward the rationalization of metabolic engineering, but also opens new processing possibilities for non-natural metabolites and novel enzymatic transformations. |
format | Online Article Text |
id | pubmed-4086079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40860792014-10-28 XTMS: pathway design in an eXTended metabolic space Carbonell, Pablo Parutto, Pierre Herisson, Joan Pandit, Shashi Bhushan Faulon, Jean-Loup Nucleic Acids Res Article As metabolic engineering and synthetic biology progress toward reaching the goal of a more sustainable use of biological resources, the need of increasing the number of value-added chemicals that can be produced in industrial organisms becomes more imperative. Exploring, however, the vast possibility of pathways amenable to engineering through heterologous genes expression in a chassis organism is complex and unattainable manually. Here, we present XTMS, a web-based pathway analysis platform available at http://xtms.issb.genopole.fr, which provides full access to the set of pathways that can be imported into a chassis organism such as Escherichia coli through the application of an Extended Metabolic Space modeling framework. The XTMS approach consists on determining the set of biochemical transformations that can potentially be processed in vivo as modeled by molecular signatures, a specific coding system for derivation of reaction rules for metabolic reactions and enumeration of all the corresponding substrates and products. Most promising routes are described in terms of metabolite exchange, maximum allowable pathway yield, toxicity and enzyme efficiency. By answering such critical design points, XTMS not only paves the road toward the rationalization of metabolic engineering, but also opens new processing possibilities for non-natural metabolites and novel enzymatic transformations. Oxford University Press 2014-07-01 2014-05-03 /pmc/articles/PMC4086079/ /pubmed/24792156 http://dx.doi.org/10.1093/nar/gku362 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Carbonell, Pablo Parutto, Pierre Herisson, Joan Pandit, Shashi Bhushan Faulon, Jean-Loup XTMS: pathway design in an eXTended metabolic space |
title | XTMS: pathway design in an eXTended metabolic space |
title_full | XTMS: pathway design in an eXTended metabolic space |
title_fullStr | XTMS: pathway design in an eXTended metabolic space |
title_full_unstemmed | XTMS: pathway design in an eXTended metabolic space |
title_short | XTMS: pathway design in an eXTended metabolic space |
title_sort | xtms: pathway design in an extended metabolic space |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086079/ https://www.ncbi.nlm.nih.gov/pubmed/24792156 http://dx.doi.org/10.1093/nar/gku362 |
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