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Flux sampling is a powerful tool to study metabolism under changing environmental conditions

The development of high-throughput ‘omic techniques has sparked a rising interest in genome-scale metabolic models, with applications ranging from disease diagnostics to crop adaptation. Efficient and accurate methods are required to analyze large metabolic networks. Flux sampling can be used to exp...

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Autores principales: Herrmann, Helena A., Dyson, Beth C., Vass, Lucy, Johnson, Giles N., Schwartz, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718391/
https://www.ncbi.nlm.nih.gov/pubmed/31482008
http://dx.doi.org/10.1038/s41540-019-0109-0
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author Herrmann, Helena A.
Dyson, Beth C.
Vass, Lucy
Johnson, Giles N.
Schwartz, Jean-Marc
author_facet Herrmann, Helena A.
Dyson, Beth C.
Vass, Lucy
Johnson, Giles N.
Schwartz, Jean-Marc
author_sort Herrmann, Helena A.
collection PubMed
description The development of high-throughput ‘omic techniques has sparked a rising interest in genome-scale metabolic models, with applications ranging from disease diagnostics to crop adaptation. Efficient and accurate methods are required to analyze large metabolic networks. Flux sampling can be used to explore the feasible flux solutions in metabolic networks by generating probability distributions of steady-state reaction fluxes. Unlike other methods, flux sampling can be used without assuming a particular cellular objective. We have undertaken a rigorous comparison of several sampling algorithms and concluded that the coordinate hit-and-run with rounding (CHRR) algorithm is the most efficient based on both run-time and multiple convergence diagnostics. We demonstrate the power of CHRR by using it to study the metabolic changes that underlie photosynthetic acclimation to cold of Arabidopsis thaliana plant leaves. In combination with experimental measurements, we show how the regulated interplay between diurnal starch and organic acid accumulation defines the plant acclimation process. We confirm fumarate accumulation as a requirement for cold acclimation and further predict γ–aminobutyric acid to have a key role in metabolic signaling under cold conditions. These results demonstrate how flux sampling can be used to analyze the feasible flux solutions across changing environmental conditions, whereas eliminating the need to make assumptions which introduce observer bias.
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spelling pubmed-67183912019-09-03 Flux sampling is a powerful tool to study metabolism under changing environmental conditions Herrmann, Helena A. Dyson, Beth C. Vass, Lucy Johnson, Giles N. Schwartz, Jean-Marc NPJ Syst Biol Appl Article The development of high-throughput ‘omic techniques has sparked a rising interest in genome-scale metabolic models, with applications ranging from disease diagnostics to crop adaptation. Efficient and accurate methods are required to analyze large metabolic networks. Flux sampling can be used to explore the feasible flux solutions in metabolic networks by generating probability distributions of steady-state reaction fluxes. Unlike other methods, flux sampling can be used without assuming a particular cellular objective. We have undertaken a rigorous comparison of several sampling algorithms and concluded that the coordinate hit-and-run with rounding (CHRR) algorithm is the most efficient based on both run-time and multiple convergence diagnostics. We demonstrate the power of CHRR by using it to study the metabolic changes that underlie photosynthetic acclimation to cold of Arabidopsis thaliana plant leaves. In combination with experimental measurements, we show how the regulated interplay between diurnal starch and organic acid accumulation defines the plant acclimation process. We confirm fumarate accumulation as a requirement for cold acclimation and further predict γ–aminobutyric acid to have a key role in metabolic signaling under cold conditions. These results demonstrate how flux sampling can be used to analyze the feasible flux solutions across changing environmental conditions, whereas eliminating the need to make assumptions which introduce observer bias. Nature Publishing Group UK 2019-09-02 /pmc/articles/PMC6718391/ /pubmed/31482008 http://dx.doi.org/10.1038/s41540-019-0109-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Herrmann, Helena A.
Dyson, Beth C.
Vass, Lucy
Johnson, Giles N.
Schwartz, Jean-Marc
Flux sampling is a powerful tool to study metabolism under changing environmental conditions
title Flux sampling is a powerful tool to study metabolism under changing environmental conditions
title_full Flux sampling is a powerful tool to study metabolism under changing environmental conditions
title_fullStr Flux sampling is a powerful tool to study metabolism under changing environmental conditions
title_full_unstemmed Flux sampling is a powerful tool to study metabolism under changing environmental conditions
title_short Flux sampling is a powerful tool to study metabolism under changing environmental conditions
title_sort flux sampling is a powerful tool to study metabolism under changing environmental conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718391/
https://www.ncbi.nlm.nih.gov/pubmed/31482008
http://dx.doi.org/10.1038/s41540-019-0109-0
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