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Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii

The regulation of metabolic networks has been shown to be distributed and shared through the action of metabolic cycles. Biochemical cycles play important roles in maintaining flux and substrate availability for multiple pathways to supply cellular energy and contribute to dynamic stability. By unde...

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Autores principales: Chapman, Stephen P., Trindade dos Santos, Marcelo, Johnson, Giles N., Kritz, Mauricio Vieira, Schwartz, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ireland 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720477/
https://www.ncbi.nlm.nih.gov/pubmed/28970020
http://dx.doi.org/10.1016/j.biosystems.2017.09.014
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author Chapman, Stephen P.
Trindade dos Santos, Marcelo
Johnson, Giles N.
Kritz, Mauricio Vieira
Schwartz, Jean-Marc
author_facet Chapman, Stephen P.
Trindade dos Santos, Marcelo
Johnson, Giles N.
Kritz, Mauricio Vieira
Schwartz, Jean-Marc
author_sort Chapman, Stephen P.
collection PubMed
description The regulation of metabolic networks has been shown to be distributed and shared through the action of metabolic cycles. Biochemical cycles play important roles in maintaining flux and substrate availability for multiple pathways to supply cellular energy and contribute to dynamic stability. By understanding the cyclic and acyclic flows of matter through a network, we are closer to understanding how complex dynamic systems distribute flux along interconnected pathways. In this work, we have applied a cycle decomposition algorithm to a genome-scale metabolic model of Chlamydomonas reinhardtii to analyse how acetate supply affects the distribution of fluxes that sustain cellular activity. We examined the role of metabolic cycles which explain the down regulation of photosynthesis that is observed when cells are grown in the presence of acetate. Our results suggest that acetate modulates changes in global metabolism, with the pentose phosphate pathway, the Calvin-Benson cycle and mitochondrial respiration activity being affected whilst reducing photosynthesis. These results show how the decomposition of metabolic flux into cyclic and acyclic components helps to understand the impact of metabolic cycling on organismal behaviour at the genome scale.
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spelling pubmed-57204772017-12-11 Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii Chapman, Stephen P. Trindade dos Santos, Marcelo Johnson, Giles N. Kritz, Mauricio Vieira Schwartz, Jean-Marc Biosystems Article The regulation of metabolic networks has been shown to be distributed and shared through the action of metabolic cycles. Biochemical cycles play important roles in maintaining flux and substrate availability for multiple pathways to supply cellular energy and contribute to dynamic stability. By understanding the cyclic and acyclic flows of matter through a network, we are closer to understanding how complex dynamic systems distribute flux along interconnected pathways. In this work, we have applied a cycle decomposition algorithm to a genome-scale metabolic model of Chlamydomonas reinhardtii to analyse how acetate supply affects the distribution of fluxes that sustain cellular activity. We examined the role of metabolic cycles which explain the down regulation of photosynthesis that is observed when cells are grown in the presence of acetate. Our results suggest that acetate modulates changes in global metabolism, with the pentose phosphate pathway, the Calvin-Benson cycle and mitochondrial respiration activity being affected whilst reducing photosynthesis. These results show how the decomposition of metabolic flux into cyclic and acyclic components helps to understand the impact of metabolic cycling on organismal behaviour at the genome scale. Elsevier Science Ireland 2017-12 /pmc/articles/PMC5720477/ /pubmed/28970020 http://dx.doi.org/10.1016/j.biosystems.2017.09.014 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chapman, Stephen P.
Trindade dos Santos, Marcelo
Johnson, Giles N.
Kritz, Mauricio Vieira
Schwartz, Jean-Marc
Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii
title Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii
title_full Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii
title_fullStr Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii
title_full_unstemmed Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii
title_short Cyclic decomposition explains a photosynthetic down regulation for Chlamydomonas reinhardtii
title_sort cyclic decomposition explains a photosynthetic down regulation for chlamydomonas reinhardtii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720477/
https://www.ncbi.nlm.nih.gov/pubmed/28970020
http://dx.doi.org/10.1016/j.biosystems.2017.09.014
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