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Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM
Fluorine is ubiquitous and the most active non-metal element in nature. While many microorganisms have developed fluoride resistance as a result of the widespread and prolonged application of oral hygiene products, the mechanisms used by these organisms to overcome fluoride toxicity are incompletely...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533749/ https://www.ncbi.nlm.nih.gov/pubmed/28754999 http://dx.doi.org/10.1038/s41598-017-06988-1 |
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author | Liu, Xiaoqing Tian, Jian Liu, Lihui Zhu, Tao Yu, Xiaoxia Chu, Xiaoyu Yao, Bin Wu, Ningfeng Fan, Yunliu |
author_facet | Liu, Xiaoqing Tian, Jian Liu, Lihui Zhu, Tao Yu, Xiaoxia Chu, Xiaoyu Yao, Bin Wu, Ningfeng Fan, Yunliu |
author_sort | Liu, Xiaoqing |
collection | PubMed |
description | Fluorine is ubiquitous and the most active non-metal element in nature. While many microorganisms have developed fluoride resistance as a result of the widespread and prolonged application of oral hygiene products, the mechanisms used by these organisms to overcome fluoride toxicity are incompletely understood. In this study, a fluoride-resistant strain, Enterobacter cloacae FRM, was identified which could grow well at a fluoride concentration of 4,000 mg/L. According to comparative genomics, transcriptome under fluoride stress, and sequence analyses of two fluoride-resistant fosmid clones, the genomic island GI3 was found to be important for fluoride resistance. The result of quantitative RT-PCR indicated that six genes on GI3, ppaC, uspA, eno, gpmA, crcB, and orf5249, which encode a fluoride transporter, fluoride-inhibited enzymes, and a universal stress protein, reside in an operon and are transcribed into two mRNAs activated by fluoride with a fluoride riboswitch. The results of knockout and complementation experiments indicated that these genes work together to provide high fluoride resistance to E. cloacae FRM. This study clarified the resistance mechanism of this high fluoride-resistant organism and has expanded our understanding of the biological effects of fluoride. |
format | Online Article Text |
id | pubmed-5533749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55337492017-08-03 Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM Liu, Xiaoqing Tian, Jian Liu, Lihui Zhu, Tao Yu, Xiaoxia Chu, Xiaoyu Yao, Bin Wu, Ningfeng Fan, Yunliu Sci Rep Article Fluorine is ubiquitous and the most active non-metal element in nature. While many microorganisms have developed fluoride resistance as a result of the widespread and prolonged application of oral hygiene products, the mechanisms used by these organisms to overcome fluoride toxicity are incompletely understood. In this study, a fluoride-resistant strain, Enterobacter cloacae FRM, was identified which could grow well at a fluoride concentration of 4,000 mg/L. According to comparative genomics, transcriptome under fluoride stress, and sequence analyses of two fluoride-resistant fosmid clones, the genomic island GI3 was found to be important for fluoride resistance. The result of quantitative RT-PCR indicated that six genes on GI3, ppaC, uspA, eno, gpmA, crcB, and orf5249, which encode a fluoride transporter, fluoride-inhibited enzymes, and a universal stress protein, reside in an operon and are transcribed into two mRNAs activated by fluoride with a fluoride riboswitch. The results of knockout and complementation experiments indicated that these genes work together to provide high fluoride resistance to E. cloacae FRM. This study clarified the resistance mechanism of this high fluoride-resistant organism and has expanded our understanding of the biological effects of fluoride. Nature Publishing Group UK 2017-07-28 /pmc/articles/PMC5533749/ /pubmed/28754999 http://dx.doi.org/10.1038/s41598-017-06988-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, Xiaoqing Tian, Jian Liu, Lihui Zhu, Tao Yu, Xiaoxia Chu, Xiaoyu Yao, Bin Wu, Ningfeng Fan, Yunliu Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM |
title | Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM |
title_full | Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM |
title_fullStr | Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM |
title_full_unstemmed | Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM |
title_short | Identification of an operon involved in fluoride resistance in Enterobacter cloacae FRM |
title_sort | identification of an operon involved in fluoride resistance in enterobacter cloacae frm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533749/ https://www.ncbi.nlm.nih.gov/pubmed/28754999 http://dx.doi.org/10.1038/s41598-017-06988-1 |
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