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Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs
BACKGROUND: When studying metabolism at the organ level, a major challenge is to understand the matter exchanges between the input and output components of the system. For example, in nutrition, biochemical models have been developed to study the metabolism of the mammary gland in relation to the sy...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925011/ https://www.ncbi.nlm.nih.gov/pubmed/24456859 http://dx.doi.org/10.1186/1752-0509-8-8 |
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author | Abdou-Arbi, Oumarou Lemosquet, Sophie Milgen, Jaap Van Siegel, Anne Bourdon, Jérémie |
author_facet | Abdou-Arbi, Oumarou Lemosquet, Sophie Milgen, Jaap Van Siegel, Anne Bourdon, Jérémie |
author_sort | Abdou-Arbi, Oumarou |
collection | PubMed |
description | BACKGROUND: When studying metabolism at the organ level, a major challenge is to understand the matter exchanges between the input and output components of the system. For example, in nutrition, biochemical models have been developed to study the metabolism of the mammary gland in relation to the synthesis of milk components. These models were designed to account for the quantitative constraints observed on inputs and outputs of the system. In these models, a compatible flux distribution is first selected. Alternatively, an infinite family of compatible set of flux rates may have to be studied when the constraints raised by observations are insufficient to identify a single flux distribution. The precursors of output nutrients are traced back with analyses similar to the computation of yield rates. However, the computation of the quantitative contributions of precursors may lack precision, mainly because some precursors are involved in the composition of several nutrients and because some metabolites are cycled in loops. RESULTS: We formally modeled the quantitative allocation of input nutrients among the branches of the metabolic network (AIO). It corresponds to yield information which, if standardized across all the outputs of the system, allows a precise quantitative understanding of their precursors. By solving nonlinear optimization problems, we introduced a method to study the variability of AIO coefficients when parsing the space of flux distributions that are compatible with both model stoichiometry and experimental data. Applied to a model of the metabolism of the mammary gland, our method made it possible to distinguish the effects of different nutritional treatments, although it cannot be proved that the mammary gland optimizes a specific linear combination of flux variables, including those based on energy. Altogether, our study indicated that the mammary gland possesses considerable metabolic flexibility. CONCLUSION: Our method enables to study the variability of a metabolic network with respect to efficiency (i.e. yield rates). It allows a quantitative comparison of the respective contributions of precursors to the production of a set of nutrients by a metabolic network, regardless of the choice of the flux distribution within the different branches of the network. |
format | Online Article Text |
id | pubmed-3925011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39250112014-03-03 Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs Abdou-Arbi, Oumarou Lemosquet, Sophie Milgen, Jaap Van Siegel, Anne Bourdon, Jérémie BMC Syst Biol Methodology Article BACKGROUND: When studying metabolism at the organ level, a major challenge is to understand the matter exchanges between the input and output components of the system. For example, in nutrition, biochemical models have been developed to study the metabolism of the mammary gland in relation to the synthesis of milk components. These models were designed to account for the quantitative constraints observed on inputs and outputs of the system. In these models, a compatible flux distribution is first selected. Alternatively, an infinite family of compatible set of flux rates may have to be studied when the constraints raised by observations are insufficient to identify a single flux distribution. The precursors of output nutrients are traced back with analyses similar to the computation of yield rates. However, the computation of the quantitative contributions of precursors may lack precision, mainly because some precursors are involved in the composition of several nutrients and because some metabolites are cycled in loops. RESULTS: We formally modeled the quantitative allocation of input nutrients among the branches of the metabolic network (AIO). It corresponds to yield information which, if standardized across all the outputs of the system, allows a precise quantitative understanding of their precursors. By solving nonlinear optimization problems, we introduced a method to study the variability of AIO coefficients when parsing the space of flux distributions that are compatible with both model stoichiometry and experimental data. Applied to a model of the metabolism of the mammary gland, our method made it possible to distinguish the effects of different nutritional treatments, although it cannot be proved that the mammary gland optimizes a specific linear combination of flux variables, including those based on energy. Altogether, our study indicated that the mammary gland possesses considerable metabolic flexibility. CONCLUSION: Our method enables to study the variability of a metabolic network with respect to efficiency (i.e. yield rates). It allows a quantitative comparison of the respective contributions of precursors to the production of a set of nutrients by a metabolic network, regardless of the choice of the flux distribution within the different branches of the network. BioMed Central 2014-01-23 /pmc/articles/PMC3925011/ /pubmed/24456859 http://dx.doi.org/10.1186/1752-0509-8-8 Text en Copyright © 2014 Abdou-Arbi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Abdou-Arbi, Oumarou Lemosquet, Sophie Milgen, Jaap Van Siegel, Anne Bourdon, Jérémie Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs |
title | Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs |
title_full | Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs |
title_fullStr | Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs |
title_full_unstemmed | Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs |
title_short | Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs |
title_sort | exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925011/ https://www.ncbi.nlm.nih.gov/pubmed/24456859 http://dx.doi.org/10.1186/1752-0509-8-8 |
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