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Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge

BACKGROUND: Pseudomonas putida is a model organism for bioremediation because of its remarkable metabolic versatility, extensive biodegradative functions, and ubiquity in contaminated soil environments. To further the understanding of molecular pathways responding to the heavy metal chromium(VI) [Cr...

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Autores principales: Thompson, Dorothea K, Chourey, Karuna, Wickham, Gene S, Thieman, Stephanie B, VerBerkmoes, Nathan C, Zhang, Bing, McCarthy, Andrea T, Rudisill, Matt A, Shah, Manesh, Hettich, Robert L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996968/
https://www.ncbi.nlm.nih.gov/pubmed/20482812
http://dx.doi.org/10.1186/1471-2164-11-311
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author Thompson, Dorothea K
Chourey, Karuna
Wickham, Gene S
Thieman, Stephanie B
VerBerkmoes, Nathan C
Zhang, Bing
McCarthy, Andrea T
Rudisill, Matt A
Shah, Manesh
Hettich, Robert L
author_facet Thompson, Dorothea K
Chourey, Karuna
Wickham, Gene S
Thieman, Stephanie B
VerBerkmoes, Nathan C
Zhang, Bing
McCarthy, Andrea T
Rudisill, Matt A
Shah, Manesh
Hettich, Robert L
author_sort Thompson, Dorothea K
collection PubMed
description BACKGROUND: Pseudomonas putida is a model organism for bioremediation because of its remarkable metabolic versatility, extensive biodegradative functions, and ubiquity in contaminated soil environments. To further the understanding of molecular pathways responding to the heavy metal chromium(VI) [Cr(VI)], the proteome of aerobically grown, Cr(VI)-stressed P. putida strain F1 was characterized within the context of two disparate nutritional environments: rich (LB) media and minimal (M9L) media containing lactate as the sole carbon source. RESULTS: Growth studies demonstrated that F1 sensitivity to Cr(VI) was impacted substantially by nutrient conditions, with a carbon-source-dependent hierarchy (lactate > glucose >> acetate) observed in minimal media. Two-dimensional HPLC-MS/MS was employed to identify differential proteome profiles generated in response to 1 mM chromate under LB and M9L growth conditions. The immediate response to Cr(VI) in LB-grown cells was up-regulation of proteins involved in inorganic ion transport, secondary metabolite biosynthesis and catabolism, and amino acid metabolism. By contrast, the chromate-responsive proteome derived under defined minimal growth conditions was characterized predominantly by up-regulated proteins related to cell envelope biogenesis, inorganic ion transport, and motility. TonB-dependent siderophore receptors involved in ferric iron acquisition and amino acid adenylation domains characterized up-regulated systems under LB-Cr(VI) conditions, while DNA repair proteins and systems scavenging sulfur from alternative sources (e.g., aliphatic sulfonates) tended to predominate the up-regulated proteome profile obtained under M9L-Cr(VI) conditions. CONCLUSIONS: Comparative analysis indicated that the core molecular response to chromate, irrespective of the nutritional conditions tested, comprised seven up-regulated proteins belonging to six different functional categories including transcription, inorganic ion transport/metabolism, and amino acid transport/metabolism. These proteins might potentially serve as indicators of chromate stress in natural microbial communities.
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spelling pubmed-29969682010-12-07 Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge Thompson, Dorothea K Chourey, Karuna Wickham, Gene S Thieman, Stephanie B VerBerkmoes, Nathan C Zhang, Bing McCarthy, Andrea T Rudisill, Matt A Shah, Manesh Hettich, Robert L BMC Genomics Research Article BACKGROUND: Pseudomonas putida is a model organism for bioremediation because of its remarkable metabolic versatility, extensive biodegradative functions, and ubiquity in contaminated soil environments. To further the understanding of molecular pathways responding to the heavy metal chromium(VI) [Cr(VI)], the proteome of aerobically grown, Cr(VI)-stressed P. putida strain F1 was characterized within the context of two disparate nutritional environments: rich (LB) media and minimal (M9L) media containing lactate as the sole carbon source. RESULTS: Growth studies demonstrated that F1 sensitivity to Cr(VI) was impacted substantially by nutrient conditions, with a carbon-source-dependent hierarchy (lactate > glucose >> acetate) observed in minimal media. Two-dimensional HPLC-MS/MS was employed to identify differential proteome profiles generated in response to 1 mM chromate under LB and M9L growth conditions. The immediate response to Cr(VI) in LB-grown cells was up-regulation of proteins involved in inorganic ion transport, secondary metabolite biosynthesis and catabolism, and amino acid metabolism. By contrast, the chromate-responsive proteome derived under defined minimal growth conditions was characterized predominantly by up-regulated proteins related to cell envelope biogenesis, inorganic ion transport, and motility. TonB-dependent siderophore receptors involved in ferric iron acquisition and amino acid adenylation domains characterized up-regulated systems under LB-Cr(VI) conditions, while DNA repair proteins and systems scavenging sulfur from alternative sources (e.g., aliphatic sulfonates) tended to predominate the up-regulated proteome profile obtained under M9L-Cr(VI) conditions. CONCLUSIONS: Comparative analysis indicated that the core molecular response to chromate, irrespective of the nutritional conditions tested, comprised seven up-regulated proteins belonging to six different functional categories including transcription, inorganic ion transport/metabolism, and amino acid transport/metabolism. These proteins might potentially serve as indicators of chromate stress in natural microbial communities. BioMed Central 2010-05-19 /pmc/articles/PMC2996968/ /pubmed/20482812 http://dx.doi.org/10.1186/1471-2164-11-311 Text en Copyright ©2010 Thompson 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
Thompson, Dorothea K
Chourey, Karuna
Wickham, Gene S
Thieman, Stephanie B
VerBerkmoes, Nathan C
Zhang, Bing
McCarthy, Andrea T
Rudisill, Matt A
Shah, Manesh
Hettich, Robert L
Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge
title Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge
title_full Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge
title_fullStr Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge
title_full_unstemmed Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge
title_short Proteomics reveals a core molecular response of Pseudomonas putida F1 to acute chromate challenge
title_sort proteomics reveals a core molecular response of pseudomonas putida f1 to acute chromate challenge
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2996968/
https://www.ncbi.nlm.nih.gov/pubmed/20482812
http://dx.doi.org/10.1186/1471-2164-11-311
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