Cargando…

Dynamic substrate preferences predict metabolic properties of a simple microbial consortium

BACKGROUND: Mixed cultures of different microbial species are increasingly being used to carry out a specific biochemical function in lieu of engineering a single microbe to do the same task. However, knowing how different species’ metabolisms will integrate to reach a desired outcome is a difficult...

Descripción completa

Detalles Bibliográficos
Autores principales: Erbilgin, Onur, Bowen, Benjamin P., Kosina, Suzanne M., Jenkins, Stefan, Lau, Rebecca K., Northen, Trent R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259839/
https://www.ncbi.nlm.nih.gov/pubmed/28114881
http://dx.doi.org/10.1186/s12859-017-1478-2
_version_ 1782499284270186496
author Erbilgin, Onur
Bowen, Benjamin P.
Kosina, Suzanne M.
Jenkins, Stefan
Lau, Rebecca K.
Northen, Trent R.
author_facet Erbilgin, Onur
Bowen, Benjamin P.
Kosina, Suzanne M.
Jenkins, Stefan
Lau, Rebecca K.
Northen, Trent R.
author_sort Erbilgin, Onur
collection PubMed
description BACKGROUND: Mixed cultures of different microbial species are increasingly being used to carry out a specific biochemical function in lieu of engineering a single microbe to do the same task. However, knowing how different species’ metabolisms will integrate to reach a desired outcome is a difficult problem that has been studied in great detail using steady-state models. However, many biotechnological processes, as well as natural habitats, represent a more dynamic system. Examining how individual species use resources in their growth medium or environment (exometabolomics) over time in batch culture conditions can provide rich phenotypic data that encompasses regulation and transporters, creating an opportunity to integrate the data into a predictive model of resource use by a mixed community. RESULTS: Here we use exometabolomic profiling to examine the time-varying substrate depletion from a mixture of 19 amino acids and glucose by two Pseudomonas and one Bacillus species isolated from ground water. Contrary to studies in model organisms, we found surprisingly few correlations between resource preferences and maximal growth rate or biomass composition. We then modeled patterns of substrate depletion, and used these models to examine if substrate usage preferences and substrate depletion kinetics of individual isolates can be used to predict the metabolism of a co-culture of the isolates. We found that most of the substrates fit the model predictions, except for glucose and histidine, which were depleted more slowly than predicted, and proline, glycine, glutamate, lysine and arginine, which were all consumed significantly faster. CONCLUSIONS: Our results indicate that a significant portion of a model community’s overall metabolism can be predicted based on the metabolism of the individuals. Based on the nature of our model, the resources that significantly deviate from the prediction highlight potential metabolic pathways affected by species-species interactions, which when further studied can potentially be used to modulate microbial community structure and/or function. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1478-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5259839
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-52598392017-01-26 Dynamic substrate preferences predict metabolic properties of a simple microbial consortium Erbilgin, Onur Bowen, Benjamin P. Kosina, Suzanne M. Jenkins, Stefan Lau, Rebecca K. Northen, Trent R. BMC Bioinformatics Research Article BACKGROUND: Mixed cultures of different microbial species are increasingly being used to carry out a specific biochemical function in lieu of engineering a single microbe to do the same task. However, knowing how different species’ metabolisms will integrate to reach a desired outcome is a difficult problem that has been studied in great detail using steady-state models. However, many biotechnological processes, as well as natural habitats, represent a more dynamic system. Examining how individual species use resources in their growth medium or environment (exometabolomics) over time in batch culture conditions can provide rich phenotypic data that encompasses regulation and transporters, creating an opportunity to integrate the data into a predictive model of resource use by a mixed community. RESULTS: Here we use exometabolomic profiling to examine the time-varying substrate depletion from a mixture of 19 amino acids and glucose by two Pseudomonas and one Bacillus species isolated from ground water. Contrary to studies in model organisms, we found surprisingly few correlations between resource preferences and maximal growth rate or biomass composition. We then modeled patterns of substrate depletion, and used these models to examine if substrate usage preferences and substrate depletion kinetics of individual isolates can be used to predict the metabolism of a co-culture of the isolates. We found that most of the substrates fit the model predictions, except for glucose and histidine, which were depleted more slowly than predicted, and proline, glycine, glutamate, lysine and arginine, which were all consumed significantly faster. CONCLUSIONS: Our results indicate that a significant portion of a model community’s overall metabolism can be predicted based on the metabolism of the individuals. Based on the nature of our model, the resources that significantly deviate from the prediction highlight potential metabolic pathways affected by species-species interactions, which when further studied can potentially be used to modulate microbial community structure and/or function. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1478-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-23 /pmc/articles/PMC5259839/ /pubmed/28114881 http://dx.doi.org/10.1186/s12859-017-1478-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Erbilgin, Onur
Bowen, Benjamin P.
Kosina, Suzanne M.
Jenkins, Stefan
Lau, Rebecca K.
Northen, Trent R.
Dynamic substrate preferences predict metabolic properties of a simple microbial consortium
title Dynamic substrate preferences predict metabolic properties of a simple microbial consortium
title_full Dynamic substrate preferences predict metabolic properties of a simple microbial consortium
title_fullStr Dynamic substrate preferences predict metabolic properties of a simple microbial consortium
title_full_unstemmed Dynamic substrate preferences predict metabolic properties of a simple microbial consortium
title_short Dynamic substrate preferences predict metabolic properties of a simple microbial consortium
title_sort dynamic substrate preferences predict metabolic properties of a simple microbial consortium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259839/
https://www.ncbi.nlm.nih.gov/pubmed/28114881
http://dx.doi.org/10.1186/s12859-017-1478-2
work_keys_str_mv AT erbilginonur dynamicsubstratepreferencespredictmetabolicpropertiesofasimplemicrobialconsortium
AT bowenbenjaminp dynamicsubstratepreferencespredictmetabolicpropertiesofasimplemicrobialconsortium
AT kosinasuzannem dynamicsubstratepreferencespredictmetabolicpropertiesofasimplemicrobialconsortium
AT jenkinsstefan dynamicsubstratepreferencespredictmetabolicpropertiesofasimplemicrobialconsortium
AT laurebeccak dynamicsubstratepreferencespredictmetabolicpropertiesofasimplemicrobialconsortium
AT northentrentr dynamicsubstratepreferencespredictmetabolicpropertiesofasimplemicrobialconsortium