Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics.

The growth of all microorganisms is limited to a specific temperature range. However, it has not previously been determined to what extent global protein profiles change in response to temperatures that incrementally span the complete growth temperature range of a microorganism. As a result it has r...

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Published in:Environmental Microbiology
Main Authors: Williams, Timothy J., Lauro, Federico M., Ertan, Haluk, Burg, Dominic W., Poljak, Anne, Raftery, Mark J., Cavicchioli, Ricardo
Format: Article in Journal/Newspaper
Language:unknown
Published: 2011
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Online Access:https://eprints.soton.ac.uk/338906/
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spelling ftsouthampton:oai:eprints.soton.ac.uk:338906 2023-07-30T03:58:39+02:00 Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics. Williams, Timothy J. Lauro, Federico M. Ertan, Haluk Burg, Dominic W. Poljak, Anne Raftery, Mark J. Cavicchioli, Ricardo 2011-08 https://eprints.soton.ac.uk/338906/ unknown Williams, Timothy J., Lauro, Federico M., Ertan, Haluk, Burg, Dominic W., Poljak, Anne, Raftery, Mark J. and Cavicchioli, Ricardo (2011) Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics. Environmental Microbiology, 13 (8), 2186-2203. (doi:10.1111/j.1462-2920.2011.02467.x <http://dx.doi.org/10.1111/j.1462-2920.2011.02467.x>). (PMID:21443741 <http://www.ncbi.nlm.nih.gov/pubmed/21443741>) Article PeerReviewed 2011 ftsouthampton https://doi.org/10.1111/j.1462-2920.2011.02467.x 2023-07-09T21:39:09Z The growth of all microorganisms is limited to a specific temperature range. However, it has not previously been determined to what extent global protein profiles change in response to temperatures that incrementally span the complete growth temperature range of a microorganism. As a result it has remained unclear to what extent cellular processes (inferred from protein abundance profiles) are affected by growth temperature and which, in particular, constrain growth at upper and lower temperature limits. To evaluate this, 8-plex iTRAQ proteomics was performed on the Antarctic microorganism, Methanococcoides burtonii. Methanococcoides burtonii was chosen due to its importance as a model psychrophilic (cold-adapted) member of the Archaea, and the fact that proteomic methods, including subcellular fractionation procedures, have been well developed. Differential abundance patterns were obtained for cells grown at seven different growth temperatures (-2°C, 1°C, 4°C, 10°C, 16°C, 23°C, 28°C) and a principal component analysis (PCA) was performed to identify trends in protein abundances. The multiplex analysis enabled three largely distinct physiological states to be described: cold stress (-2°C), cold adaptation (1°C, 4°C, 10°C and 16°C), and heat stress (23°C and 28°C). A particular feature of the thermal extremes was the synthesis of heat- and cold-specific stress proteins, reflecting the important, yet distinct ways in which temperature-induced stress manifests in the cell. This is the first quantitative proteomic investigation to simultaneously assess the response of a microorganism to numerous growth temperatures, including the upper and lower growth temperatures limits, and has revealed a new level of understanding about cellular adaptive responses. Article in Journal/Newspaper Antarc* Antarctic University of Southampton: e-Prints Soton Antarctic The Antarctic Environmental Microbiology 13 8 2186 2203
institution Open Polar
collection University of Southampton: e-Prints Soton
op_collection_id ftsouthampton
language unknown
description The growth of all microorganisms is limited to a specific temperature range. However, it has not previously been determined to what extent global protein profiles change in response to temperatures that incrementally span the complete growth temperature range of a microorganism. As a result it has remained unclear to what extent cellular processes (inferred from protein abundance profiles) are affected by growth temperature and which, in particular, constrain growth at upper and lower temperature limits. To evaluate this, 8-plex iTRAQ proteomics was performed on the Antarctic microorganism, Methanococcoides burtonii. Methanococcoides burtonii was chosen due to its importance as a model psychrophilic (cold-adapted) member of the Archaea, and the fact that proteomic methods, including subcellular fractionation procedures, have been well developed. Differential abundance patterns were obtained for cells grown at seven different growth temperatures (-2°C, 1°C, 4°C, 10°C, 16°C, 23°C, 28°C) and a principal component analysis (PCA) was performed to identify trends in protein abundances. The multiplex analysis enabled three largely distinct physiological states to be described: cold stress (-2°C), cold adaptation (1°C, 4°C, 10°C and 16°C), and heat stress (23°C and 28°C). A particular feature of the thermal extremes was the synthesis of heat- and cold-specific stress proteins, reflecting the important, yet distinct ways in which temperature-induced stress manifests in the cell. This is the first quantitative proteomic investigation to simultaneously assess the response of a microorganism to numerous growth temperatures, including the upper and lower growth temperatures limits, and has revealed a new level of understanding about cellular adaptive responses.
format Article in Journal/Newspaper
author Williams, Timothy J.
Lauro, Federico M.
Ertan, Haluk
Burg, Dominic W.
Poljak, Anne
Raftery, Mark J.
Cavicchioli, Ricardo
spellingShingle Williams, Timothy J.
Lauro, Federico M.
Ertan, Haluk
Burg, Dominic W.
Poljak, Anne
Raftery, Mark J.
Cavicchioli, Ricardo
Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics.
author_facet Williams, Timothy J.
Lauro, Federico M.
Ertan, Haluk
Burg, Dominic W.
Poljak, Anne
Raftery, Mark J.
Cavicchioli, Ricardo
author_sort Williams, Timothy J.
title Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics.
title_short Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics.
title_full Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics.
title_fullStr Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics.
title_full_unstemmed Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics.
title_sort defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°c to 28°c) using multiplex quantitative proteomics.
publishDate 2011
url https://eprints.soton.ac.uk/338906/
geographic Antarctic
The Antarctic
geographic_facet Antarctic
The Antarctic
genre Antarc*
Antarctic
genre_facet Antarc*
Antarctic
op_relation Williams, Timothy J., Lauro, Federico M., Ertan, Haluk, Burg, Dominic W., Poljak, Anne, Raftery, Mark J. and Cavicchioli, Ricardo (2011) Defining the response of a microorganism to temperatures that span its complete growth temperature range (-2°C to 28°C) using multiplex quantitative proteomics. Environmental Microbiology, 13 (8), 2186-2203. (doi:10.1111/j.1462-2920.2011.02467.x <http://dx.doi.org/10.1111/j.1462-2920.2011.02467.x>). (PMID:21443741 <http://www.ncbi.nlm.nih.gov/pubmed/21443741>)
op_doi https://doi.org/10.1111/j.1462-2920.2011.02467.x
container_title Environmental Microbiology
container_volume 13
container_issue 8
container_start_page 2186
op_container_end_page 2203
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