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Clémence Frioux

Publications and source records attributed to Clémence Frioux.

2 recordsLinked to original sources

Prediction of source nutrients for microorganisms using metabolic networks

Metagenomics has lowered the barrier to microbial discovery--enabling the identification of novel microbes without isolation--but cultures remain imperative for the deep study of microbes. Cultivation and isolation of non-model microbes remains a major challenge, despite advances in high-throughput culturomic methods. The quantity of simultaneous experimental variables is constrained by time and resources, but the list can be reduced using computational biology. Given an annotated genome, metabolic modelling can be used to predict source nutrients required for the growth of a microbe, which acts as an initial screen to inform culture and isolation experiments. This chapter provides an overview of metabolic networks and modelling and how they can be used to predict the nutrient requirements of a microorganism, followed by a sample protocol using a toy metabolic network, which is then expanded to a genome-scale metabolic network application. These methods can be applied to any metabolic network of interest--which in turn can be created from any genome of interest--and are a starting point for experimental validation of source nutrients required for microorganisms that remain uncultivated to date.

q-bio.MN↗

Hybrid Metabolic Network Completion

Metabolic networks play a crucial role in biology since they capture all chemical reactions in an organism. While there are networks of high quality for many model organisms, networks for less studied organisms are often of poor quality and suffer from incompleteness. To this end, we introduced in previous work an ASP-based approach to metabolic network completion. Although this qualitative approach allows for restoring moderately degraded networks, it fails to restore highly degraded ones. This is because it ignores quantitative constraints capturing reaction rates. To address this problem, we propose a hybrid approach to metabolic network completion that integrates our qualitative ASP approach with quantitative means for capturing reaction rates. We begin by formally reconciling existing stoichiometric and topological approaches to network completion in a unified formalism. With it, we develop a hybrid ASP encoding and rely upon the theory reasoning capacities of the ASP system clingo for solving the resulting logic program with linear constraints over reals. We empirically evaluate our approach by means of the metabolic network of Escherichia coli. Our analysis shows that our novel approach yields greatly superior results than obtainable from purely qualitative or quantitative approaches. Under consideration in Theory and Practice of Logic Programming (TPLP).

cs.LO↗