XTMS: pathway design in an eXTended metabolic space

Pablo Carbonell, Pierre Parutto, Joan Herisson, Shashi B Pandit, Jean-Loup Faulon

    Research output: Contribution to journalArticlepeer-review

    Abstract

    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.
    Original languageEnglish
    Pages (from-to)W389-W394
    JournalNucleic acids research
    Volume42
    Issue number42 (W1)
    DOIs
    Publication statusPublished - 3 May 2014

    Keywords

    • metabolic\_engineering
    • metabolic\_space
    • pathway
    • promiscuity
    • synthetic\_biology

    Research Beacons, Institutes and Platforms

    • Manchester Institute of Biotechnology

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