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Metabolic networks for nitrogen utilization in Prevotella ruminicola23

Nitrogen metabolism in gut systems remains poorly studied in spite of its importance for microbial growth and its implications for the metabolism of the host. Prevotella spp. are the most predominant bacteria detected in the rumen, but their presence has also been related to health and disease state...

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Autores principales: Kim, Jong Nam, Méndez–García, Celia, Geier, Renae R., Iakiviak, Michael, Chang, Jongsoo, Cann, Isaac, Mackie, Roderick I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552732/
https://www.ncbi.nlm.nih.gov/pubmed/28798330
http://dx.doi.org/10.1038/s41598-017-08463-3
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author Kim, Jong Nam
Méndez–García, Celia
Geier, Renae R.
Iakiviak, Michael
Chang, Jongsoo
Cann, Isaac
Mackie, Roderick I.
author_facet Kim, Jong Nam
Méndez–García, Celia
Geier, Renae R.
Iakiviak, Michael
Chang, Jongsoo
Cann, Isaac
Mackie, Roderick I.
author_sort Kim, Jong Nam
collection PubMed
description Nitrogen metabolism in gut systems remains poorly studied in spite of its importance for microbial growth and its implications for the metabolism of the host. Prevotella spp. are the most predominant bacteria detected in the rumen, but their presence has also been related to health and disease states in the human gut and oral cavity. To explore the metabolic networks for nitrogen assimilation in this bacterium, changes in gene expression profiles in response to variations in the available nitrogen source and to different concentrations of ammonium were analyzed by microarray and reverse transcription quantitative PCR, and linked with function by further proteomic analysis. The observed patterns of transcript abundances for genes involved in ammonium assimilation differed from the classical “enteric paradigm” for nitrogen utilization. Expression of genes encoding high substrate affinity nitrogen assimilation enzymes (GS-GOGAT system) was similar in growth-limiting and non-limiting nitrogen concentrations in P. ruminicola 23, whereas E. coli and Salmonella spp. responses to excess nitrogen involve only low substrate affinity enzymes. This versatile behavior might be a key feature for ecological success in habitats such as the rumen and human colon where nitrogen is rarely limiting for growth, and might be linked to previously reported Prevotella spp. population imbalances relative to other bacterial species in gut systems.
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spelling pubmed-55527322017-08-14 Metabolic networks for nitrogen utilization in Prevotella ruminicola23 Kim, Jong Nam Méndez–García, Celia Geier, Renae R. Iakiviak, Michael Chang, Jongsoo Cann, Isaac Mackie, Roderick I. Sci Rep Article Nitrogen metabolism in gut systems remains poorly studied in spite of its importance for microbial growth and its implications for the metabolism of the host. Prevotella spp. are the most predominant bacteria detected in the rumen, but their presence has also been related to health and disease states in the human gut and oral cavity. To explore the metabolic networks for nitrogen assimilation in this bacterium, changes in gene expression profiles in response to variations in the available nitrogen source and to different concentrations of ammonium were analyzed by microarray and reverse transcription quantitative PCR, and linked with function by further proteomic analysis. The observed patterns of transcript abundances for genes involved in ammonium assimilation differed from the classical “enteric paradigm” for nitrogen utilization. Expression of genes encoding high substrate affinity nitrogen assimilation enzymes (GS-GOGAT system) was similar in growth-limiting and non-limiting nitrogen concentrations in P. ruminicola 23, whereas E. coli and Salmonella spp. responses to excess nitrogen involve only low substrate affinity enzymes. This versatile behavior might be a key feature for ecological success in habitats such as the rumen and human colon where nitrogen is rarely limiting for growth, and might be linked to previously reported Prevotella spp. population imbalances relative to other bacterial species in gut systems. Nature Publishing Group UK 2017-08-10 /pmc/articles/PMC5552732/ /pubmed/28798330 http://dx.doi.org/10.1038/s41598-017-08463-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Jong Nam
Méndez–García, Celia
Geier, Renae R.
Iakiviak, Michael
Chang, Jongsoo
Cann, Isaac
Mackie, Roderick I.
Metabolic networks for nitrogen utilization in Prevotella ruminicola23
title Metabolic networks for nitrogen utilization in Prevotella ruminicola23
title_full Metabolic networks for nitrogen utilization in Prevotella ruminicola23
title_fullStr Metabolic networks for nitrogen utilization in Prevotella ruminicola23
title_full_unstemmed Metabolic networks for nitrogen utilization in Prevotella ruminicola23
title_short Metabolic networks for nitrogen utilization in Prevotella ruminicola23
title_sort metabolic networks for nitrogen utilization in prevotella ruminicola23
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552732/
https://www.ncbi.nlm.nih.gov/pubmed/28798330
http://dx.doi.org/10.1038/s41598-017-08463-3
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