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A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism

Phototrophic organisms such as cyanobacteria utilize the sun’s energy to convert atmospheric carbon dioxide into organic carbon, resulting in diurnal variations in the cell’s metabolism. Flux balance analysis is a widely accepted constraint-based optimization tool for analyzing growth and metabolism...

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Autores principales: Sarkar, Debolina, Mueller, Thomas J., Liu, Deng, Pakrasi, Himadri B., Maranas, Costas D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6364703/
https://www.ncbi.nlm.nih.gov/pubmed/30677028
http://dx.doi.org/10.1371/journal.pcbi.1006692
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author Sarkar, Debolina
Mueller, Thomas J.
Liu, Deng
Pakrasi, Himadri B.
Maranas, Costas D.
author_facet Sarkar, Debolina
Mueller, Thomas J.
Liu, Deng
Pakrasi, Himadri B.
Maranas, Costas D.
author_sort Sarkar, Debolina
collection PubMed
description Phototrophic organisms such as cyanobacteria utilize the sun’s energy to convert atmospheric carbon dioxide into organic carbon, resulting in diurnal variations in the cell’s metabolism. Flux balance analysis is a widely accepted constraint-based optimization tool for analyzing growth and metabolism, but it is generally used in a time-invariant manner with no provisions for sequestering different biomass components at different time periods. Here we present CycleSyn, a periodic model of Synechocystis sp. PCC 6803 metabolism that spans a 12-hr light/12-hr dark cycle by segmenting it into 12 Time Point Models (TPMs) with a uniform duration of two hours. The developed framework allows for the flow of metabolites across TPMs while inventorying metabolite levels and only allowing for the utilization of currently or previously produced compounds. The 12 TPMs allow for the incorporation of time-dependent constraints that capture the cyclic nature of cellular processes. Imposing bounds on reactions informed by temporally-segmented transcriptomic data enables simulation of phototrophic growth as a single linear programming (LP) problem. The solution provides the time varying reaction fluxes over a 24-hour cycle and the accumulation/consumption of metabolites. The diurnal rhythm of metabolic gene expression driven by the circadian clock and its metabolic consequences is explored. Predicted flux and metabolite pools are in line with published studies regarding the temporal organization of phototrophic growth in Synechocystis PCC 6803 paving the way for constructing time-resolved genome-scale models (GSMs) for organisms with a circadian clock. In addition, the metabolic reorganization that would be required to enable Synechocystis PCC 6803 to temporally separate photosynthesis from oxygen-sensitive nitrogen fixation is also explored using the developed model formalism.
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spelling pubmed-63647032019-02-15 A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism Sarkar, Debolina Mueller, Thomas J. Liu, Deng Pakrasi, Himadri B. Maranas, Costas D. PLoS Comput Biol Research Article Phototrophic organisms such as cyanobacteria utilize the sun’s energy to convert atmospheric carbon dioxide into organic carbon, resulting in diurnal variations in the cell’s metabolism. Flux balance analysis is a widely accepted constraint-based optimization tool for analyzing growth and metabolism, but it is generally used in a time-invariant manner with no provisions for sequestering different biomass components at different time periods. Here we present CycleSyn, a periodic model of Synechocystis sp. PCC 6803 metabolism that spans a 12-hr light/12-hr dark cycle by segmenting it into 12 Time Point Models (TPMs) with a uniform duration of two hours. The developed framework allows for the flow of metabolites across TPMs while inventorying metabolite levels and only allowing for the utilization of currently or previously produced compounds. The 12 TPMs allow for the incorporation of time-dependent constraints that capture the cyclic nature of cellular processes. Imposing bounds on reactions informed by temporally-segmented transcriptomic data enables simulation of phototrophic growth as a single linear programming (LP) problem. The solution provides the time varying reaction fluxes over a 24-hour cycle and the accumulation/consumption of metabolites. The diurnal rhythm of metabolic gene expression driven by the circadian clock and its metabolic consequences is explored. Predicted flux and metabolite pools are in line with published studies regarding the temporal organization of phototrophic growth in Synechocystis PCC 6803 paving the way for constructing time-resolved genome-scale models (GSMs) for organisms with a circadian clock. In addition, the metabolic reorganization that would be required to enable Synechocystis PCC 6803 to temporally separate photosynthesis from oxygen-sensitive nitrogen fixation is also explored using the developed model formalism. Public Library of Science 2019-01-24 /pmc/articles/PMC6364703/ /pubmed/30677028 http://dx.doi.org/10.1371/journal.pcbi.1006692 Text en © 2019 Sarkar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sarkar, Debolina
Mueller, Thomas J.
Liu, Deng
Pakrasi, Himadri B.
Maranas, Costas D.
A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism
title A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism
title_full A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism
title_fullStr A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism
title_full_unstemmed A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism
title_short A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism
title_sort diurnal flux balance model of synechocystis sp. pcc 6803 metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6364703/
https://www.ncbi.nlm.nih.gov/pubmed/30677028
http://dx.doi.org/10.1371/journal.pcbi.1006692
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