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A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton

We present a model of the growth rate and elemental stoichiometry of phytoplankton as a function of resource allocation between and within broad macromolecular pools under a variety of resource supply conditions. The model is based on four, empirically-supported, cornerstone assumptions: that there...

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Autores principales: Inomura, Keisuke, Omta, Anne Willem, Talmy, David, Bragg, Jason, Deutsch, Curtis, Follows, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093025/
https://www.ncbi.nlm.nih.gov/pubmed/32256456
http://dx.doi.org/10.3389/fmicb.2020.00086
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author Inomura, Keisuke
Omta, Anne Willem
Talmy, David
Bragg, Jason
Deutsch, Curtis
Follows, Michael J.
author_facet Inomura, Keisuke
Omta, Anne Willem
Talmy, David
Bragg, Jason
Deutsch, Curtis
Follows, Michael J.
author_sort Inomura, Keisuke
collection PubMed
description We present a model of the growth rate and elemental stoichiometry of phytoplankton as a function of resource allocation between and within broad macromolecular pools under a variety of resource supply conditions. The model is based on four, empirically-supported, cornerstone assumptions: that there is a saturating relationship between light and photosynthesis, a linear relationship between RNA/protein and growth rate, a linear relationship between biosynthetic proteins and growth rate, and a constant macromolecular composition of the light-harvesting machinery. We combine these assumptions with statements of conservation of carbon, nitrogen, phosphorus, and energy. The model can be solved algebraically for steady state conditions and constrained with data on elemental stoichiometry from published laboratory chemostat studies. It interprets the relationships between macromolecular and elemental stoichiometry and also provides quantitative predictions of the maximum growth rate at given light intensity and nutrient supply rates. The model is compatible with data sets from several laboratory studies characterizing both prokaryotic and eukaryotic phytoplankton from marine and freshwater environments. It is conceptually simple, yet mechanistic and quantitative. Here, the model is constrained only by elemental stoichiometry, but makes predictions about allocation to measurable macromolecular pools, which could be tested in the laboratory.
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spelling pubmed-70930252020-03-31 A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton Inomura, Keisuke Omta, Anne Willem Talmy, David Bragg, Jason Deutsch, Curtis Follows, Michael J. Front Microbiol Microbiology We present a model of the growth rate and elemental stoichiometry of phytoplankton as a function of resource allocation between and within broad macromolecular pools under a variety of resource supply conditions. The model is based on four, empirically-supported, cornerstone assumptions: that there is a saturating relationship between light and photosynthesis, a linear relationship between RNA/protein and growth rate, a linear relationship between biosynthetic proteins and growth rate, and a constant macromolecular composition of the light-harvesting machinery. We combine these assumptions with statements of conservation of carbon, nitrogen, phosphorus, and energy. The model can be solved algebraically for steady state conditions and constrained with data on elemental stoichiometry from published laboratory chemostat studies. It interprets the relationships between macromolecular and elemental stoichiometry and also provides quantitative predictions of the maximum growth rate at given light intensity and nutrient supply rates. The model is compatible with data sets from several laboratory studies characterizing both prokaryotic and eukaryotic phytoplankton from marine and freshwater environments. It is conceptually simple, yet mechanistic and quantitative. Here, the model is constrained only by elemental stoichiometry, but makes predictions about allocation to measurable macromolecular pools, which could be tested in the laboratory. Frontiers Media S.A. 2020-02-28 /pmc/articles/PMC7093025/ /pubmed/32256456 http://dx.doi.org/10.3389/fmicb.2020.00086 Text en Copyright © 2020 Inomura, Omta, Talmy, Bragg, Deutsch and Follows. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Inomura, Keisuke
Omta, Anne Willem
Talmy, David
Bragg, Jason
Deutsch, Curtis
Follows, Michael J.
A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton
title A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton
title_full A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton
title_fullStr A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton
title_full_unstemmed A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton
title_short A Mechanistic Model of Macromolecular Allocation, Elemental Stoichiometry, and Growth Rate in Phytoplankton
title_sort mechanistic model of macromolecular allocation, elemental stoichiometry, and growth rate in phytoplankton
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093025/
https://www.ncbi.nlm.nih.gov/pubmed/32256456
http://dx.doi.org/10.3389/fmicb.2020.00086
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