Abstract

BackgroundDue to the growing amount of biological knowledge that is incorporated into metabolic network models, their analysis has become more and more challenging. Here, we examine the capabilities of the recently introduced chemical organization theory (OT) to ease this task. Considering only network stoichiometry, the theory allows the prediction of all potentially persistent species sets and therewith rigorously relates the structure of a network to its potential dynamics. By this, the phenotypes implied by a metabolic network can be predicted without the need for explicit knowledge of the detailed reaction kinetics.ResultsWe propose an approach to deal with regulation – and especially inhibitory interactions – in chemical organization theory. One advantage of this approach is that the metabolic network and its regulation are represented in an integrated way as one reaction network. To demonstrate the feasibility of this approach we examine a model by Covert and Palsson (J Biol Chem, 277(31), 2002) of the central metabolism of E. coli that incorporates the regulation of all involved genes. Our method correctly predicts the known growth phenotypes on 16 different substrates. Without specific assumptions, organization theory correctly predicts the lethality of knockout experiments in 101 out of 116 cases. Taking into account the same model specific assumptions as in the regulatory flux balance analysis (rFBA) by Covert and Palsson, the same performance is achieved (106 correctly predicted cases). Two model specific assumptions had to be considered: first, we have to assume that secreted molecules do not influence the regulatory system, and second, that metabolites with increasing concentrations indicate a lethal state.ConclusionThe introduced approach to model a metabolic network and its regulation in an integrated way as one reaction network makes organization analysis a universal technique to study the potential behavior of biological network models. Applying multiple methods like OT and rFBA is shown to be valuable to uncover critical assumptions and helps to improve model coherence.

Highlights

  • Due to the growing amount of biological knowledge that is incorporated into metabolic network models, their analysis has become more and more challenging

  • We apply the method to a model of the central metabolism of E. coli by Covert and Palsson [19]

  • With model specific assumptions, "adapted" organization theory was able to predict the lethality of knockout experiments correctly in 106 cases (91.4%), achieving the same performance as regulatory flux balance analysis (rFBA) [19]

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Summary

Introduction

Due to the growing amount of biological knowledge that is incorporated into metabolic network models, their analysis has become more and more challenging. Important results have been obtained by applying methods like flux balance analysis [1], modeling by differential equations [2], stochastic simulations [3], or elementary flux mode analysis [4]. Its basic aim is to identify parts of the network, or more precisely, sets of molecular species, that are likely to coexist on a long time scale without any of the species vanishing or other species appearing anew. This encompasses steady states of the network as might be identified by elementary flux mode analysis As negative regulation for some genes was ignored because the down-regulation of genes cannot push gene expression levels below the basal level, some organizations represented biologically infeasible system states, for example the simultaneous uptake of all carbon sources

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