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Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor

The abundance of two-component systems (TCSs) in Streptomyces coelicolor A3(2) genome indicates their importance in the physiology of this soil bacteria. Currently, several TCSs have been related to antibiotic regulation, and the purpose in this study was the characterization of five TCSs, selected...

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Autores principales: Yepes, Ana, Rico, Sergio, Rodríguez-García, Antonio, Santamaría, Ramón I., Díaz, Margarita
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098853/
https://www.ncbi.nlm.nih.gov/pubmed/21625497
http://dx.doi.org/10.1371/journal.pone.0019980
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author Yepes, Ana
Rico, Sergio
Rodríguez-García, Antonio
Santamaría, Ramón I.
Díaz, Margarita
author_facet Yepes, Ana
Rico, Sergio
Rodríguez-García, Antonio
Santamaría, Ramón I.
Díaz, Margarita
author_sort Yepes, Ana
collection PubMed
description The abundance of two-component systems (TCSs) in Streptomyces coelicolor A3(2) genome indicates their importance in the physiology of this soil bacteria. Currently, several TCSs have been related to antibiotic regulation, and the purpose in this study was the characterization of five TCSs, selected by sequence homology with the well-known absA1A2 system, that could also be associated with this important process. Null mutants of the five TCSs were obtained and two mutants (ΔSCO1744/1745 and ΔSCO4596/4597/4598) showed significant differences in both antibiotic production and morphological differentiation, and have been renamed as abr (antibiotic regulator). No detectable changes in antibiotic production were found in the mutants in the systems that include the ORFs SCO3638/3639, SCO3640/3641 and SCO2165/2166 in any of the culture conditions assayed. The system SCO1744/1745 (AbrA1/A2) was involved in negative regulation of antibiotic production, and acted also as a negative regulator of the morphological differentiation. By contrast, the system SCO4596/4597/4598 (AbrC1/C2/C3), composed of two histidine kinases and one response regulator, had positive effects on both morphological development and antibiotic production. Microarray analyses of the ΔabrC1/C2/C3 and wild-type transcriptomes revealed downregulation of actII-ORF4 and cdaR genes, the actinorhodin and calcium-dependent antibiotic pathway-specific regulators respectively. These results demonstrated the involvement of these new two-component systems in antibiotic production and morphological differentiation by different approaches. One is a pleiotropic negative regulator: abrA1/A2. The other one is a positive regulator composed of three elements, two histidine kinases and one response regulator: abrC1/C2/C3.
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spelling pubmed-30988532011-05-27 Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor Yepes, Ana Rico, Sergio Rodríguez-García, Antonio Santamaría, Ramón I. Díaz, Margarita PLoS One Research Article The abundance of two-component systems (TCSs) in Streptomyces coelicolor A3(2) genome indicates their importance in the physiology of this soil bacteria. Currently, several TCSs have been related to antibiotic regulation, and the purpose in this study was the characterization of five TCSs, selected by sequence homology with the well-known absA1A2 system, that could also be associated with this important process. Null mutants of the five TCSs were obtained and two mutants (ΔSCO1744/1745 and ΔSCO4596/4597/4598) showed significant differences in both antibiotic production and morphological differentiation, and have been renamed as abr (antibiotic regulator). No detectable changes in antibiotic production were found in the mutants in the systems that include the ORFs SCO3638/3639, SCO3640/3641 and SCO2165/2166 in any of the culture conditions assayed. The system SCO1744/1745 (AbrA1/A2) was involved in negative regulation of antibiotic production, and acted also as a negative regulator of the morphological differentiation. By contrast, the system SCO4596/4597/4598 (AbrC1/C2/C3), composed of two histidine kinases and one response regulator, had positive effects on both morphological development and antibiotic production. Microarray analyses of the ΔabrC1/C2/C3 and wild-type transcriptomes revealed downregulation of actII-ORF4 and cdaR genes, the actinorhodin and calcium-dependent antibiotic pathway-specific regulators respectively. These results demonstrated the involvement of these new two-component systems in antibiotic production and morphological differentiation by different approaches. One is a pleiotropic negative regulator: abrA1/A2. The other one is a positive regulator composed of three elements, two histidine kinases and one response regulator: abrC1/C2/C3. Public Library of Science 2011-05-20 /pmc/articles/PMC3098853/ /pubmed/21625497 http://dx.doi.org/10.1371/journal.pone.0019980 Text en Yepes et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yepes, Ana
Rico, Sergio
Rodríguez-García, Antonio
Santamaría, Ramón I.
Díaz, Margarita
Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor
title Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor
title_full Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor
title_fullStr Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor
title_full_unstemmed Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor
title_short Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor
title_sort novel two-component systems implied in antibiotic production in streptomyces coelicolor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098853/
https://www.ncbi.nlm.nih.gov/pubmed/21625497
http://dx.doi.org/10.1371/journal.pone.0019980
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