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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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 |
work_keys_str_mv |
AT fadouaelmoustaid photorespirationandratesynchronizationinaphototrophheterotrophmicrobialconsortium AT rosspcarlson photorespirationandratesynchronizationinaphototrophheterotrophmicrobialconsortium AT federicavilla photorespirationandratesynchronizationinaphototrophheterotrophmicrobialconsortium AT isaacklapper photorespirationandratesynchronizationinaphototrophheterotrophmicrobialconsortium |
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1725050615115022336 |