Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial Consortium

Theprocessofoxygenicphotosynthesisisrobustandubiquitous,relyingcentrallyoninput of light, carbon dioxide, and water, which in many environments are all abundantly available, and from which are produced, principally, oxygen and reduced organic carbon. However, photosynthetic machinery can be conflicte...

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Main Authors: Fadoua El Moustaid, Ross P. Carlson, Federica Villa, Isaac Klapper
Format: Article
Language:English
Published: MDPI AG 2017-03-01
Series:Processes
Subjects:
Online Access:http://www.mdpi.com/2227-9717/5/1/11
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spelling doaj-b8890ec745824240b088d908fc7812b82020-11-25T01:39:04ZengMDPI AGProcesses2227-97172017-03-01511110.3390/pr5010011pr5010011Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial ConsortiumFadoua El Moustaid0Ross P. Carlson1Federica Villa2Isaac Klapper3Department of Biological Sciences, Virginia Tech University, Blacksburg, VA 24061, USACenter for Biofilm Engineering, Montana State University, Bozeman, MT 59717, USADepartment of Food, Environmental and Nutritional Sciences, Università degli Studi di Milano, 20133 Milano, ItalyDepartment of Mathematics, Temple University, Philadelphia, PA 19122, USATheprocessofoxygenicphotosynthesisisrobustandubiquitous,relyingcentrallyoninput of light, carbon dioxide, and water, which in many environments are all abundantly available, and from which are produced, principally, oxygen and reduced organic carbon. However, photosynthetic machinery can be conflicted by the simultaneous presence of carbon dioxide and oxygen through a process sometimes called photorespiration. We present here a model of phototrophy, including competition for RuBisCO binding sites between oxygen and carbon dioxide, in a chemostat-based microbial population. The model connects to the idea of metabolic pathways to track carbon and degree of reduction through the system. We find decomposition of kinetics into elementary flux modes a mathematically natural way to study synchronization of mismatched rates of photon input and chemostat turnover. In the single species case, though total biomass is reduced by photorespiration, protection from excess light exposures and its consequences (oxidative and redox stress) may result. We also find the possibility that a consortium of phototrophs with heterotrophs can recycle photorespiration byproduct into increased biomass at the cost of increase in oxidative product (here, oxygen).http://www.mdpi.com/2227-9717/5/1/11photosynthesisphotorespirationchemostat modelphototroph-heterotroph consortium
collection DOAJ
language English
format Article
sources DOAJ
author Fadoua El Moustaid
Ross P. Carlson
Federica Villa
Isaac Klapper
spellingShingle Fadoua El Moustaid
Ross P. Carlson
Federica Villa
Isaac Klapper
Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial Consortium
Processes
photosynthesis
photorespiration
chemostat model
phototroph-heterotroph consortium
author_facet Fadoua El Moustaid
Ross P. Carlson
Federica Villa
Isaac Klapper
author_sort Fadoua El Moustaid
title Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial Consortium
title_short Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial Consortium
title_full Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial Consortium
title_fullStr Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial Consortium
title_full_unstemmed Photorespiration and Rate Synchronization in a Phototroph-Heterotroph Microbial Consortium
title_sort photorespiration and rate synchronization in a phototroph-heterotroph microbial consortium
publisher MDPI AG
series Processes
issn 2227-9717
publishDate 2017-03-01
description Theprocessofoxygenicphotosynthesisisrobustandubiquitous,relyingcentrallyoninput of light, carbon dioxide, and water, which in many environments are all abundantly available, and from which are produced, principally, oxygen and reduced organic carbon. However, photosynthetic machinery can be conflicted by the simultaneous presence of carbon dioxide and oxygen through a process sometimes called photorespiration. We present here a model of phototrophy, including competition for RuBisCO binding sites between oxygen and carbon dioxide, in a chemostat-based microbial population. The model connects to the idea of metabolic pathways to track carbon and degree of reduction through the system. We find decomposition of kinetics into elementary flux modes a mathematically natural way to study synchronization of mismatched rates of photon input and chemostat turnover. In the single species case, though total biomass is reduced by photorespiration, protection from excess light exposures and its consequences (oxidative and redox stress) may result. We also find the possibility that a consortium of phototrophs with heterotrophs can recycle photorespiration byproduct into increased biomass at the cost of increase in oxidative product (here, oxygen).
topic photosynthesis
photorespiration
chemostat model
phototroph-heterotroph consortium
url http://www.mdpi.com/2227-9717/5/1/11
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AT rosspcarlson photorespirationandratesynchronizationinaphototrophheterotrophmicrobialconsortium
AT federicavilla photorespirationandratesynchronizationinaphototrophheterotrophmicrobialconsortium
AT isaacklapper photorespirationandratesynchronizationinaphototrophheterotrophmicrobialconsortium
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