Cargando…

An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92

BACKGROUND: Yersinia pestis is a gram-negative bacterium that causes plague, a disease linked historically to the Black Death in Europe during the Middle Ages and to several outbreaks during the modern era. Metabolism in Y. pestis displays remarkable flexibility and robustness, allowing the bacteriu...

Descripción completa

Detalles Bibliográficos
Autores principales: Charusanti, Pep, Chauhan, Sadhana, McAteer, Kathleen, Lerman, Joshua A, Hyduke, Daniel R, Motin, Vladimir L, Ansong, Charles, Adkins, Joshua N, Palsson, Bernhard O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220653/
https://www.ncbi.nlm.nih.gov/pubmed/21995956
http://dx.doi.org/10.1186/1752-0509-5-163
_version_ 1782216981817065472
author Charusanti, Pep
Chauhan, Sadhana
McAteer, Kathleen
Lerman, Joshua A
Hyduke, Daniel R
Motin, Vladimir L
Ansong, Charles
Adkins, Joshua N
Palsson, Bernhard O
author_facet Charusanti, Pep
Chauhan, Sadhana
McAteer, Kathleen
Lerman, Joshua A
Hyduke, Daniel R
Motin, Vladimir L
Ansong, Charles
Adkins, Joshua N
Palsson, Bernhard O
author_sort Charusanti, Pep
collection PubMed
description BACKGROUND: Yersinia pestis is a gram-negative bacterium that causes plague, a disease linked historically to the Black Death in Europe during the Middle Ages and to several outbreaks during the modern era. Metabolism in Y. pestis displays remarkable flexibility and robustness, allowing the bacterium to proliferate in both warm-blooded mammalian hosts and cold-blooded insect vectors such as fleas. RESULTS: Here we report a genome-scale reconstruction and mathematical model of metabolism for Y. pestis CO92 and supporting experimental growth and metabolite measurements. The model contains 815 genes, 678 proteins, 963 unique metabolites and 1678 reactions, accurately simulates growth on a range of carbon sources both qualitatively and quantitatively, and identifies gaps in several key biosynthetic pathways and suggests how those gaps might be filled. Furthermore, our model presents hypotheses to explain certain known nutritional requirements characteristic of this strain. CONCLUSIONS: Y. pestis continues to be a dangerous threat to human health during modern times. The Y. pestis genome-scale metabolic reconstruction presented here, which has been benchmarked against experimental data and correctly reproduces known phenotypes, provides an in silico platform with which to investigate the metabolism of this important human pathogen.
format Online
Article
Text
id pubmed-3220653
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-32206532011-11-21 An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92 Charusanti, Pep Chauhan, Sadhana McAteer, Kathleen Lerman, Joshua A Hyduke, Daniel R Motin, Vladimir L Ansong, Charles Adkins, Joshua N Palsson, Bernhard O BMC Syst Biol Research Article BACKGROUND: Yersinia pestis is a gram-negative bacterium that causes plague, a disease linked historically to the Black Death in Europe during the Middle Ages and to several outbreaks during the modern era. Metabolism in Y. pestis displays remarkable flexibility and robustness, allowing the bacterium to proliferate in both warm-blooded mammalian hosts and cold-blooded insect vectors such as fleas. RESULTS: Here we report a genome-scale reconstruction and mathematical model of metabolism for Y. pestis CO92 and supporting experimental growth and metabolite measurements. The model contains 815 genes, 678 proteins, 963 unique metabolites and 1678 reactions, accurately simulates growth on a range of carbon sources both qualitatively and quantitatively, and identifies gaps in several key biosynthetic pathways and suggests how those gaps might be filled. Furthermore, our model presents hypotheses to explain certain known nutritional requirements characteristic of this strain. CONCLUSIONS: Y. pestis continues to be a dangerous threat to human health during modern times. The Y. pestis genome-scale metabolic reconstruction presented here, which has been benchmarked against experimental data and correctly reproduces known phenotypes, provides an in silico platform with which to investigate the metabolism of this important human pathogen. BioMed Central 2011-10-13 /pmc/articles/PMC3220653/ /pubmed/21995956 http://dx.doi.org/10.1186/1752-0509-5-163 Text en Copyright ©2011 Charusanti et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Charusanti, Pep
Chauhan, Sadhana
McAteer, Kathleen
Lerman, Joshua A
Hyduke, Daniel R
Motin, Vladimir L
Ansong, Charles
Adkins, Joshua N
Palsson, Bernhard O
An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92
title An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92
title_full An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92
title_fullStr An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92
title_full_unstemmed An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92
title_short An experimentally-supported genome-scale metabolic network reconstruction for Yersinia pestis CO92
title_sort experimentally-supported genome-scale metabolic network reconstruction for yersinia pestis co92
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220653/
https://www.ncbi.nlm.nih.gov/pubmed/21995956
http://dx.doi.org/10.1186/1752-0509-5-163
work_keys_str_mv AT charusantipep anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT chauhansadhana anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT mcateerkathleen anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT lermanjoshuaa anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT hydukedanielr anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT motinvladimirl anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT ansongcharles anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT adkinsjoshuan anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT palssonbernhardo anexperimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT charusantipep experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT chauhansadhana experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT mcateerkathleen experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT lermanjoshuaa experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT hydukedanielr experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT motinvladimirl experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT ansongcharles experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT adkinsjoshuan experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92
AT palssonbernhardo experimentallysupportedgenomescalemetabolicnetworkreconstructionforyersiniapestisco92