Abstract

Bacterial phenotypic traits and lifestyles in response to diverse environmental conditions depend on changes in the internal molecular environment. However, predicting bacterial adaptability is still difficult outside of laboratory controlled conditions. Many molecular levels can contribute to the adaptation to a changing environment: pathway structure, codon usage, metabolism. To measure adaptability to changing environmental conditions and over time, we develop a multi-omic model of Escherichia coli that accounts for metabolism, gene expression and codon usage at both transcription and translation levels. After the integration of multiple omics into the model, we propose a multiobjective optimization algorithm to find the allowable and optimal metabolic phenotypes through concurrent maximization or minimization of multiple metabolic markers. In the condition space, we propose Pareto hypervolume and spectral analysis as estimators of short term multi-omic (transcriptomic and metabolic) evolution, thus enabling comparative analysis of metabolic conditions. We therefore compare, evaluate and cluster different experimental conditions, models and bacterial strains according to their metabolic response in a multidimensional objective space, rather than in the original space of microarray data. We finally validate our methods on a phenomics dataset of growth conditions. Our framework, named METRADE, is freely available as a MATLAB toolbox.

Highlights

  • Recently produced for several organisms, including Escherichia coli[7], Clostridium[8], Salmonella[9], and fission yeast[10]

  • Since each profile is associated with a growth condition, the objective space becomes the condition phase-space, which we investigate through principal component analysis, pseudospectra, and a spectral method for community detection

  • We derive a multi-omic model for the Escherichia coli able to account for the adaptability to multiple environmental conditions, and for the temporal evolution towards the production of selected metabolites

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Summary

Introduction

Recently produced for several organisms, including Escherichia coli[7], Clostridium[8], Salmonella[9], and fission yeast[10]. The advantage of our approach is that it allows studying bacterial adaptability across multiple objectives (including biomass yield) in changing environmental settings, with the possibility to add available ‘omic data between gene expression and reaction rates by adjusting a continuous map. It requires only accurate information on the biochemical reaction system—provided by the full reaction list of the organism—and does not rely on knowledge of the kinetics of the system, which is usually missing. METRADE is validated against a recently published phenomics compendium of growth conditions, and is made available in the Supplementary Information as a toolbox extension of COBRA 2.015

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