Metabolic complementation in bacterial communities: necessary conditions and optimality
Bacterial communities may display metabolic complementation, in which different members of the association partially contribute to the same biosynthetic pathway. In this way, the end product of the pathway is synthesized by the community as a whole. However, the emergence and the benefits of such co...
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doaj-8fdab08a68d943a7b6b35cade36e1ece2020-11-24T20:51:54ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2016-10-01710.3389/fmicb.2016.01553220494Metabolic complementation in bacterial communities: necessary conditions and optimalityMatteo Mori0Matteo Mori1Miguel Ponce De León2Juli Peretó3Francisco Montero4Universidad Complutense de MadridUniversity of California San DiegoUniversidad Complutense de MadridUniversitat de València-CSICUniversidad Complutense de MadridBacterial communities may display metabolic complementation, in which different members of the association partially contribute to the same biosynthetic pathway. In this way, the end product of the pathway is synthesized by the community as a whole. However, the emergence and the benefits of such complementation are poorly understood. Herein we present a simple model to analyze the metabolic interactions among bacteria, including the host in the case of endosymbiotic bacteria. The model considers two cell populations, with both cell types encoding for the same linear biosynthetic pathway. We have found that, for metabolic complementation to emerge as an optimal strategy, both product inhibition and large permeabilities are needed. In the light of these results, we then consider the patterns found in the case of tryptophan biosynthesis in the endosymbiont consortium hosted by the aphid Cinara cedri. Using in-silico computed physicochemical properties of metabolites of this and other biosynthetic pathways, we verified that the splitting point of the pathway corresponds to the most permeable intermediate.http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01553/fulloptimizationendosymbiotic bacteriakinetic modelingMetabolic Modellingcross-feedingMetabolic complementation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Matteo Mori Matteo Mori Miguel Ponce De León Juli Peretó Francisco Montero |
spellingShingle |
Matteo Mori Matteo Mori Miguel Ponce De León Juli Peretó Francisco Montero Metabolic complementation in bacterial communities: necessary conditions and optimality Frontiers in Microbiology optimization endosymbiotic bacteria kinetic modeling Metabolic Modelling cross-feeding Metabolic complementation |
author_facet |
Matteo Mori Matteo Mori Miguel Ponce De León Juli Peretó Francisco Montero |
author_sort |
Matteo Mori |
title |
Metabolic complementation in bacterial communities: necessary conditions and optimality |
title_short |
Metabolic complementation in bacterial communities: necessary conditions and optimality |
title_full |
Metabolic complementation in bacterial communities: necessary conditions and optimality |
title_fullStr |
Metabolic complementation in bacterial communities: necessary conditions and optimality |
title_full_unstemmed |
Metabolic complementation in bacterial communities: necessary conditions and optimality |
title_sort |
metabolic complementation in bacterial communities: necessary conditions and optimality |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Microbiology |
issn |
1664-302X |
publishDate |
2016-10-01 |
description |
Bacterial communities may display metabolic complementation, in which different members of the association partially contribute to the same biosynthetic pathway. In this way, the end product of the pathway is synthesized by the community as a whole. However, the emergence and the benefits of such complementation are poorly understood. Herein we present a simple model to analyze the metabolic interactions among bacteria, including the host in the case of endosymbiotic bacteria. The model considers two cell populations, with both cell types encoding for the same linear biosynthetic pathway. We have found that, for metabolic complementation to emerge as an optimal strategy, both product inhibition and large permeabilities are needed. In the light of these results, we then consider the patterns found in the case of tryptophan biosynthesis in the endosymbiont consortium hosted by the aphid Cinara cedri. Using in-silico computed physicochemical properties of metabolites of this and other biosynthetic pathways, we verified that the splitting point of the pathway corresponds to the most permeable intermediate. |
topic |
optimization endosymbiotic bacteria kinetic modeling Metabolic Modelling cross-feeding Metabolic complementation |
url |
http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01553/full |
work_keys_str_mv |
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