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PMID: 12547764 Published · ppublish English Evaluation Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Validation Study

Analysis of metabolic capabilities using singular value decomposition of extreme pathway matrices.

Biophysical journal ·Vol. 84 ·No. 2 Pt 1 ·2003-02-00 ·Pages 794-804

Price ND, Reed JL, Papin JA, Famili I, Palsson BO

Abstract

It is now possible to construct genome-scale metabolic networks for particular microorganisms. Extreme pathway analysis is a useful method for analyzing the phenotypic capabilities of these networks. Many extreme pathways are needed to fully describe the functional capabilities of genome-scale metabolic networks, and therefore, a need exists to develop methods to study these large sets of extreme pathways. Singular value decomposition (SVD) of matrices of extreme pathways was used to develop a conceptual framework for the interpretation of large sets of extreme pathways and the steady-state flux solution space they define. The key results of this study were: 1), convex steady-state solution cones describing the potential functions of biochemical networks can be studied using the modes generated by SVD; 2), Helicobacter pylori has a more rigid metabolic network (i.e., a lower dimensional solution space and a more dominant first singular value) than Haemophilus influenzae for the production of amino acids; and 3), SVD allows for direct comparison of different solution cones resulting from the production of different amino acids. SVD was used to identify key network branch points that may identify key control points for regulation. Therefore, SVD of matrices of extreme pathways has proved to be a useful method for analyzing the steady-state solution space of genome-scale metabolic networks.

MeSH Terms
Algorithms Amino Acids/biosynthesis Energy Metabolism/genetics,physiology Gene Expression Regulation, Bacterial/physiology Genome, Bacterial Genomics/methods Haemophilus influenzae/genetics,metabolism,physiology Helicobacter pylori/genetics,metabolism Models, Biological Quality Control Signal Transduction/genetics,physiology
Chemicals
Amino Acids
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Price Nathan D
Department of Bioengineering, University of California/San Diego, La Jolla, California 92093-0412, USA.
Reed Jennifer L
Papin Jason A
Famili Iman
Palsson Bernhard O
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
2003-02-00
Pages
794-804
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1302660
Subset
IM
Grants
NIGMS NIH HHS · R01 GM057089 · United States
NIGMS NIH HHS · GM 57089 · United States
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