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Tracing regulatory routes in metabolism using generalised supply-demand analysis

BACKGROUND: Generalised supply-demand analysis is a conceptual framework that views metabolism as a molecular economy. Metabolic pathways are partitioned into so-called supply and demand blocks that produce and consume a particular intermediate metabolite. By studying the response of these reaction...

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Autores principales: Christensen, Carl D., Hofmeyr, Jan-Hendrik S., Rohwer, Johann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669674/
https://www.ncbi.nlm.nih.gov/pubmed/26635009
http://dx.doi.org/10.1186/s12918-015-0236-1
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author Christensen, Carl D.
Hofmeyr, Jan-Hendrik S.
Rohwer, Johann M.
author_facet Christensen, Carl D.
Hofmeyr, Jan-Hendrik S.
Rohwer, Johann M.
author_sort Christensen, Carl D.
collection PubMed
description BACKGROUND: Generalised supply-demand analysis is a conceptual framework that views metabolism as a molecular economy. Metabolic pathways are partitioned into so-called supply and demand blocks that produce and consume a particular intermediate metabolite. By studying the response of these reaction blocks to perturbations in the concentration of the linking metabolite, different regulatory routes of interaction between the metabolite and its supply and demand blocks can be identified and their contribution quantified. These responses are mediated not only through direct substrate/product interactions, but also through allosteric effects. Here we subject previously published kinetic models of pyruvate metabolism in Lactococcus lactis and aspartate-derived amino acid synthesis in Arabidopsis thaliana to generalised supply-demand analysis. RESULTS: Multiple routes of regulation are brought about by different mechanisms in each model, leading to behavioural and regulatory patterns that are generally difficult to predict from simple inspection of the reaction networks depicting the models. In the pyruvate model the moiety-conserved cycles of ATP/ADP and NADH/NAD (+) allow otherwise independent metabolic branches to communicate. This causes the flux of one ATP-producing reaction block to increase in response to an increasing ATP/ADP ratio, while an NADH-consuming block flux decreases in response to an increasing NADH/NAD (+) ratio for certain ratio value ranges. In the aspartate model, aspartate semialdehyde can inhibit its supply block directly or by increasing the concentration of two amino acids (Lys and Thr) that occur as intermediates in demand blocks and act as allosteric inhibitors of isoenzymes in the supply block. These different routes of interaction from aspartate semialdehyde are each seen to contribute differently to the regulation of the aspartate semialdehyde supply block. CONCLUSIONS: Indirect routes of regulation between a metabolic intermediate and a reaction block that either produces or consumes this intermediate can play a much larger regulatory role than routes mediated through direct interactions. These indirect routes of regulation can also result in counter-intuitive metabolic behaviour. Performing generalised supply-demand analysis on two previously published models demonstrated the utility of this method as an entry point in the analysis of metabolic behaviour and the potential for obtaining novel results from previously analysed models by using new approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-015-0236-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-46696742015-12-05 Tracing regulatory routes in metabolism using generalised supply-demand analysis Christensen, Carl D. Hofmeyr, Jan-Hendrik S. Rohwer, Johann M. BMC Syst Biol Research Article BACKGROUND: Generalised supply-demand analysis is a conceptual framework that views metabolism as a molecular economy. Metabolic pathways are partitioned into so-called supply and demand blocks that produce and consume a particular intermediate metabolite. By studying the response of these reaction blocks to perturbations in the concentration of the linking metabolite, different regulatory routes of interaction between the metabolite and its supply and demand blocks can be identified and their contribution quantified. These responses are mediated not only through direct substrate/product interactions, but also through allosteric effects. Here we subject previously published kinetic models of pyruvate metabolism in Lactococcus lactis and aspartate-derived amino acid synthesis in Arabidopsis thaliana to generalised supply-demand analysis. RESULTS: Multiple routes of regulation are brought about by different mechanisms in each model, leading to behavioural and regulatory patterns that are generally difficult to predict from simple inspection of the reaction networks depicting the models. In the pyruvate model the moiety-conserved cycles of ATP/ADP and NADH/NAD (+) allow otherwise independent metabolic branches to communicate. This causes the flux of one ATP-producing reaction block to increase in response to an increasing ATP/ADP ratio, while an NADH-consuming block flux decreases in response to an increasing NADH/NAD (+) ratio for certain ratio value ranges. In the aspartate model, aspartate semialdehyde can inhibit its supply block directly or by increasing the concentration of two amino acids (Lys and Thr) that occur as intermediates in demand blocks and act as allosteric inhibitors of isoenzymes in the supply block. These different routes of interaction from aspartate semialdehyde are each seen to contribute differently to the regulation of the aspartate semialdehyde supply block. CONCLUSIONS: Indirect routes of regulation between a metabolic intermediate and a reaction block that either produces or consumes this intermediate can play a much larger regulatory role than routes mediated through direct interactions. These indirect routes of regulation can also result in counter-intuitive metabolic behaviour. Performing generalised supply-demand analysis on two previously published models demonstrated the utility of this method as an entry point in the analysis of metabolic behaviour and the potential for obtaining novel results from previously analysed models by using new approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12918-015-0236-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-03 /pmc/articles/PMC4669674/ /pubmed/26635009 http://dx.doi.org/10.1186/s12918-015-0236-1 Text en © Christensen et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Christensen, Carl D.
Hofmeyr, Jan-Hendrik S.
Rohwer, Johann M.
Tracing regulatory routes in metabolism using generalised supply-demand analysis
title Tracing regulatory routes in metabolism using generalised supply-demand analysis
title_full Tracing regulatory routes in metabolism using generalised supply-demand analysis
title_fullStr Tracing regulatory routes in metabolism using generalised supply-demand analysis
title_full_unstemmed Tracing regulatory routes in metabolism using generalised supply-demand analysis
title_short Tracing regulatory routes in metabolism using generalised supply-demand analysis
title_sort tracing regulatory routes in metabolism using generalised supply-demand analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669674/
https://www.ncbi.nlm.nih.gov/pubmed/26635009
http://dx.doi.org/10.1186/s12918-015-0236-1
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