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An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27
Arsenic resistance is commonly clustered in ars operons in bacteria; main ars operon components encode an arsenate reductase, a membrane extrusion protein, and an As‐sensitive transcription factor. In the As‐resistant thermophile Thermus thermophilus HB27, genes encoding homologues of these proteins...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658604/ https://www.ncbi.nlm.nih.gov/pubmed/28696001 http://dx.doi.org/10.1111/1751-7915.12761 |
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author | Antonucci, Immacolata Gallo, Giovanni Limauro, Danila Contursi, Patrizia Ribeiro, Ana Luisa Blesa, Alba Berenguer, José Bartolucci, Simonetta Fiorentino, Gabriella |
author_facet | Antonucci, Immacolata Gallo, Giovanni Limauro, Danila Contursi, Patrizia Ribeiro, Ana Luisa Blesa, Alba Berenguer, José Bartolucci, Simonetta Fiorentino, Gabriella |
author_sort | Antonucci, Immacolata |
collection | PubMed |
description | Arsenic resistance is commonly clustered in ars operons in bacteria; main ars operon components encode an arsenate reductase, a membrane extrusion protein, and an As‐sensitive transcription factor. In the As‐resistant thermophile Thermus thermophilus HB27, genes encoding homologues of these proteins are interspersed in the chromosome. In this article, we show that two adjacent genes, TtsmtB, encoding an ArsR/SmtB transcriptional repressor and, TTC0354, encoding a Zn(2+)/Cd(2+)‐dependent membrane ATPase are involved in As resistance; differently from characterized ars operons, the two genes are transcribed from dedicated promoters upstream of their respective genes, whose expression is differentially regulated at transcriptional level. Mutants defective in TtsmtB or TTC0354 are more sensitive to As than the wild type, proving their role in arsenic resistance. Recombinant dimeric TtSmtB binds in vitro to both promoters, but its binding capability decreases upon interaction with arsenate and, less efficiently, with arsenite. In vivo and in vitro experiments also demonstrate that the arsenate reductase (TtArsC) is subjected to regulation by TtSmtB. We propose a model for the regulation of As resistance in T. thermophilus in which TtSmtB is the arsenate sensor responsible for the induction of TtArsC which generates arsenite exported by TTC0354 efflux protein to detoxify cells. |
format | Online Article Text |
id | pubmed-5658604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56586042017-11-01 An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27 Antonucci, Immacolata Gallo, Giovanni Limauro, Danila Contursi, Patrizia Ribeiro, Ana Luisa Blesa, Alba Berenguer, José Bartolucci, Simonetta Fiorentino, Gabriella Microb Biotechnol Research Articles Arsenic resistance is commonly clustered in ars operons in bacteria; main ars operon components encode an arsenate reductase, a membrane extrusion protein, and an As‐sensitive transcription factor. In the As‐resistant thermophile Thermus thermophilus HB27, genes encoding homologues of these proteins are interspersed in the chromosome. In this article, we show that two adjacent genes, TtsmtB, encoding an ArsR/SmtB transcriptional repressor and, TTC0354, encoding a Zn(2+)/Cd(2+)‐dependent membrane ATPase are involved in As resistance; differently from characterized ars operons, the two genes are transcribed from dedicated promoters upstream of their respective genes, whose expression is differentially regulated at transcriptional level. Mutants defective in TtsmtB or TTC0354 are more sensitive to As than the wild type, proving their role in arsenic resistance. Recombinant dimeric TtSmtB binds in vitro to both promoters, but its binding capability decreases upon interaction with arsenate and, less efficiently, with arsenite. In vivo and in vitro experiments also demonstrate that the arsenate reductase (TtArsC) is subjected to regulation by TtSmtB. We propose a model for the regulation of As resistance in T. thermophilus in which TtSmtB is the arsenate sensor responsible for the induction of TtArsC which generates arsenite exported by TTC0354 efflux protein to detoxify cells. John Wiley and Sons Inc. 2017-07-11 /pmc/articles/PMC5658604/ /pubmed/28696001 http://dx.doi.org/10.1111/1751-7915.12761 Text en © 2017 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Antonucci, Immacolata Gallo, Giovanni Limauro, Danila Contursi, Patrizia Ribeiro, Ana Luisa Blesa, Alba Berenguer, José Bartolucci, Simonetta Fiorentino, Gabriella An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27 |
title | An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27 |
title_full | An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27 |
title_fullStr | An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27 |
title_full_unstemmed | An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27 |
title_short | An ArsR/SmtB family member regulates arsenic resistance genes unusually arranged in Thermus thermophilus HB27 |
title_sort | arsr/smtb family member regulates arsenic resistance genes unusually arranged in thermus thermophilus hb27 |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658604/ https://www.ncbi.nlm.nih.gov/pubmed/28696001 http://dx.doi.org/10.1111/1751-7915.12761 |
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