Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803
Arsenic is one of the most important global environmental pollutants. Here we show that the cyanobacterium Synechocystis sp. strain PCC 6803 contains an arsenic and antimony resistance operon consisting of three genes: arsB, encoding a putative arsenite and antimonite carrier, arsH, encoding a prote...
| Autores: | , , |
|---|---|
| Formato: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2003 |
| País: | España |
| Recursos: | Universidad de Sevilla (US) |
| Repositorio: | idUS. Depósito de Investigación de la Universidad de Sevilla |
| OAI Identifier: | oai:idus.us.es:11441/62954 |
| Acesso em linha: | http://hdl.handle.net/11441/62954 https://doi.org/10.1128/JB.185.18.5363-5371.2003 |
| Access Level: | acceso abierto |
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Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803López Maury, LuisFlorencio Bellido, Francisco JavierReyes Rosa, José CarlosArsenic is one of the most important global environmental pollutants. Here we show that the cyanobacterium Synechocystis sp. strain PCC 6803 contains an arsenic and antimony resistance operon consisting of three genes: arsB, encoding a putative arsenite and antimonite carrier, arsH, encoding a protein of unknown function, and arsC, encoding a putative arsenate reductase. While arsB mutant strains were sensitive to arsenite, arsenate, and antimonite, arsC mutants were sensitive only to arsenate. The arsH mutant strain showed no obvious phenotype under the conditions tested. In vivo the arsBHC operon was derepressed by oxyanions of arsenic and antimony (oxidation state, +3) and, to a lesser extent, by bismuth (oxidation state, +3) and arsenate (oxidation state, +5). In the absence of these effectors, the operon was repressed by a transcription repressor of the ArsR/SmtB family, encoded by an unlinked gene termed arsR. Thus, arsR null mutants showed constitutive derepression of the arsBHC operon. Expression of the arsR gene was not altered by the presence of arsenic or antimony compounds. Purified recombinant ArsR protein binds to the arsBHC promoter-operator region in the absence of metals and dissociates from the DNA in the presence of Sb(III) or As(III) but not in the presence of As(V), suggesting that trivalent metalloids are the true inducers of the system. DNase I footprinting experiments indicate that ArsR binds to two 17-bp direct repeats, with each one consisting of two inverted repeats, in the region from nucleotides -34 to + 17 of the arsBHC promoter-operator.Ministerio de Ciencia y Tecnología BMC2001-2635Junta de Andalucía CV1-802American Society for MicrobiologyBioquímica Vegetal y Biología MolecularMinisterio de Ciencia y Tecnología (MCYT). EspañaJunta de Andalucía2003info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/11441/62954https://doi.org/10.1128/JB.185.18.5363-5371.2003reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésJournal of Bacteriology, 185 (18), 5363-5371.BMC2001-2635CV1-802http://dx.doi.org/10.1128/JB.185.18.5363-5371.2003info:eu-repo/semantics/openAccessoai:idus.us.es:11441/629542026-06-17T12:51:07Z |
| dc.title.none.fl_str_mv |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 |
| title |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 |
| spellingShingle |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 López Maury, Luis |
| title_short |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 |
| title_full |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 |
| title_fullStr |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 |
| title_full_unstemmed |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 |
| title_sort |
Arsenic sensing and resistance system in the cyanobacterium Synechocystis sp. Strain PCC 6803 |
| dc.creator.none.fl_str_mv |
López Maury, Luis Florencio Bellido, Francisco Javier Reyes Rosa, José Carlos |
| author |
López Maury, Luis |
| author_facet |
López Maury, Luis Florencio Bellido, Francisco Javier Reyes Rosa, José Carlos |
| author_role |
author |
| author2 |
Florencio Bellido, Francisco Javier Reyes Rosa, José Carlos |
| author2_role |
author author |
| dc.contributor.none.fl_str_mv |
Bioquímica Vegetal y Biología Molecular Ministerio de Ciencia y Tecnología (MCYT). España Junta de Andalucía |
| description |
Arsenic is one of the most important global environmental pollutants. Here we show that the cyanobacterium Synechocystis sp. strain PCC 6803 contains an arsenic and antimony resistance operon consisting of three genes: arsB, encoding a putative arsenite and antimonite carrier, arsH, encoding a protein of unknown function, and arsC, encoding a putative arsenate reductase. While arsB mutant strains were sensitive to arsenite, arsenate, and antimonite, arsC mutants were sensitive only to arsenate. The arsH mutant strain showed no obvious phenotype under the conditions tested. In vivo the arsBHC operon was derepressed by oxyanions of arsenic and antimony (oxidation state, +3) and, to a lesser extent, by bismuth (oxidation state, +3) and arsenate (oxidation state, +5). In the absence of these effectors, the operon was repressed by a transcription repressor of the ArsR/SmtB family, encoded by an unlinked gene termed arsR. Thus, arsR null mutants showed constitutive derepression of the arsBHC operon. Expression of the arsR gene was not altered by the presence of arsenic or antimony compounds. Purified recombinant ArsR protein binds to the arsBHC promoter-operator region in the absence of metals and dissociates from the DNA in the presence of Sb(III) or As(III) but not in the presence of As(V), suggesting that trivalent metalloids are the true inducers of the system. DNase I footprinting experiments indicate that ArsR binds to two 17-bp direct repeats, with each one consisting of two inverted repeats, in the region from nucleotides -34 to + 17 of the arsBHC promoter-operator. |
| publishDate |
2003 |
| dc.date.none.fl_str_mv |
2003 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11441/62954 https://doi.org/10.1128/JB.185.18.5363-5371.2003 |
| url |
http://hdl.handle.net/11441/62954 https://doi.org/10.1128/JB.185.18.5363-5371.2003 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Journal of Bacteriology, 185 (18), 5363-5371. BMC2001-2635 CV1-802 http://dx.doi.org/10.1128/JB.185.18.5363-5371.2003 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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American Society for Microbiology |
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American Society for Microbiology |
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reponame:idUS. Depósito de Investigación de la Universidad de Sevilla instname:Universidad de Sevilla (US) |
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Universidad de Sevilla (US) |
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