Elucidation and Structural Analysis of Conserved Pools for Genome-Scale Metabolic Reconstructions

¹ The Pennsylvania State University

^* To whom correspondence should be addressed. E-mail: costas{at}psu.edu.

Submitted on March 25, 2004
Revised on July 11, 2004
Accepted on 21 September 2004

	Abstract

In this paper, we introduce Metabolite Concentration Coupling Analysis (MCCA) to study conservation relationships for metabolite concentrations in genome-scale metabolic networks. The analysis allows the global identification of subsets of metabolites whose concentrations are always coupled within common conserved pools. Also, the Minimal Conserved Pool Identification (MCPI) procedure is developed for elucidating conserved pools for targeted metabolites without computing the entire basis conservation relationships. The approaches are demonstrated on genome-scale metabolic reconstructions of Helicobacter pylori, Escherichia coli, and Saccharomyces cerevisiae. Despite significant differences in the size and complexity of the examined organism's models, we find that the concentrations of nearly all metabolites are coupled within a relatively small number of subsets. These correspond to the overall exchange of carbon molecules into and out of the networks, interconversion of energy and redox cofactors, and the transfer of nitrogen, sulfur, phosphate, coenzyme A, and acyl carrier protein moieties among metabolites. The presence of large conserved pools can be viewed as global biophysical barriers protecting cellular systems from stresses, maintaining coordinated interconversions between key metabolites, and providing an additional mode of global metabolic regulation. The developed approaches thus provide novel and versatile tools for elucidating coupling relationships between metabolite concentrations with implications in biotechnological and medical applications.

Key Words: conserved metabolite pools, genome-scale metabolic reconstructions, pathway modeling, stoichiometric models

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