Abstract

BackgroundThe emergence of functions in biological systems is a long-standing issue that can now be addressed at the cell level with the emergence of high throughput technologies for genome sequencing and phenotyping. The reconstruction of complete metabolic networks for various organisms is a key outcome of the analysis of these data, giving access to a global view of cell functioning. The analysis of metabolic networks may be carried out by simply considering the architecture of the reaction network or by taking into account the stoichiometry of reactions. In both approaches, this analysis is generally centered on the outcome of the network and considers all metabolic compounds to be equivalent in this respect. As in the case of genes and reactions, about which the concept of essentiality has been developed, it seems, however, that some metabolites play crucial roles in system responses, due to the cell structure or the internal wiring of the metabolic network.ResultsWe propose a classification of metabolic compounds according to their capacity to influence the activation of targeted functions (generally the growth phenotype) in a cell. We generalize the concept of essentiality to metabolites and introduce the concept of the phenotypic essential metabolite (PEM) which influences the growth phenotype according to sustainability, producibility or optimal-efficiency criteria. We have developed and made available a tool, Conquests, which implements a method combining graph-based and flux-based analysis, two approaches that are usually considered separately. The identification of PEMs is made effective by using a logical programming approach.ConclusionThe exhaustive study of phenotypic essential metabolites in six genome-scale metabolic models suggests that the combination and the comparison of graph, stoichiometry and optimal flux-based criteria allows some features of the metabolic network functionality to be deciphered by focusing on a small number of compounds. By considering the best combination of both graph-based and flux-based techniques, the Conquests python package advocates for a broader use of these compounds both to facilitate network curation and to promote a precise understanding of metabolic phenotype.

Highlights

  • Deciphering phenotypic features of organisms is a fundamental pursuit in Biology (Kauffman, 1992)

  • We introduce three classes of phenotypic essential metabolites (PEM), corresponding to three different semantics for a metabolic network functionality

  • In order to introduce the definition of phenotypic essential metabolites, we shall point out metabolic compounds that play an important role with respect to the activation of a specific targeted reaction

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Summary

Introduction

Deciphering phenotypic features of organisms is a fundamental pursuit in Biology (Kauffman, 1992). Once the network structure is judged satisfactory (Ebenhoh & Heinrich, 2003; Liberal & Pinney, 2013), other techniques are applied by considering additional constraints such as mass-balance equilibrium (or stoichiometry) of internal compounds (i.e., Elementary Flux Modes (Schuster, Dandekar & Fell, 1999), Flux Coupling Analysis (Burgard et al, 2004) or Minimal Cut Sets (Klamt & Gilles, 2004; Beurton-Aimar, Nguyen & Colombie, 2014)). The exhaustive study of phenotypic essential metabolites in six genomescale metabolic models suggests that the combination and the comparison of graph, stoichiometry and optimal flux-based criteria allows some features of the metabolic network functionality to be deciphered by focusing on a small number of compounds

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