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Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1

Previously, the expression of arsenite [As(III)] oxidase genes aioBA was reported to be regulated by a three-component regulatory system, AioXSR, in a number of As(III)-oxidizing bacterial strains. However, the regulation mechanism is still unknown when aioXSR genes are absent in some As(III)-oxidiz...

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Autores principales: Chen, Fang, Cao, Yajing, Wei, Sha, Li, Yanzhi, Li, Xiangyang, Wang, Qian, Wang, Gejiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563254/
https://www.ncbi.nlm.nih.gov/pubmed/26441863
http://dx.doi.org/10.3389/fmicb.2015.00923
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author Chen, Fang
Cao, Yajing
Wei, Sha
Li, Yanzhi
Li, Xiangyang
Wang, Qian
Wang, Gejiao
author_facet Chen, Fang
Cao, Yajing
Wei, Sha
Li, Yanzhi
Li, Xiangyang
Wang, Qian
Wang, Gejiao
author_sort Chen, Fang
collection PubMed
description Previously, the expression of arsenite [As(III)] oxidase genes aioBA was reported to be regulated by a three-component regulatory system, AioXSR, in a number of As(III)-oxidizing bacterial strains. However, the regulation mechanism is still unknown when aioXSR genes are absent in some As(III)-oxidizing bacterial genomes, such as in Halomonas sp. HAL1. In this study, transposon mutagenesis and gene knock-out mutation were performed, and two mutants, HAL1-phoR(931) and HAL1-▵phoB, were obtained in strain HAL1. The phoR and phoB constitute a two-component system which is responsible for phosphate (Pi) acquisition and assimilation. Both of the mutants showed negative As(III)-oxidation phenotypes in low Pi condition (0.1 mM) but not under normal Pi condition (1 mM). The phoBR complementation strain HAL1-▵phoB-C reversed the mutants' null phenotypes back to wild type status. Meanwhile, lacZ reporter fusions using pCM-lacZ showed that the expression of phoBR and aioBA were both induced by As(III) but were not induced in HAL1-phoR(931) and HAL1-▵phoB. Using 15 consensus Pho box sequences, a putative Pho box was found in the aioBA regulation region. PhoB was able to bind to the putative Pho box in vivo (bacterial one-hybrid detection) and in vitro (electrophoretic mobility gel shift assay), and an 18-bp binding sequence containing nine conserved bases were determined. This study provided the evidence that PhoBR regulates the expression of aioBA in Halomonas sp. HAL1 under low Pi condition. The new regulation model further implies the close metabolic connection between As and Pi.
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spelling pubmed-45632542015-10-05 Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1 Chen, Fang Cao, Yajing Wei, Sha Li, Yanzhi Li, Xiangyang Wang, Qian Wang, Gejiao Front Microbiol Microbiology Previously, the expression of arsenite [As(III)] oxidase genes aioBA was reported to be regulated by a three-component regulatory system, AioXSR, in a number of As(III)-oxidizing bacterial strains. However, the regulation mechanism is still unknown when aioXSR genes are absent in some As(III)-oxidizing bacterial genomes, such as in Halomonas sp. HAL1. In this study, transposon mutagenesis and gene knock-out mutation were performed, and two mutants, HAL1-phoR(931) and HAL1-▵phoB, were obtained in strain HAL1. The phoR and phoB constitute a two-component system which is responsible for phosphate (Pi) acquisition and assimilation. Both of the mutants showed negative As(III)-oxidation phenotypes in low Pi condition (0.1 mM) but not under normal Pi condition (1 mM). The phoBR complementation strain HAL1-▵phoB-C reversed the mutants' null phenotypes back to wild type status. Meanwhile, lacZ reporter fusions using pCM-lacZ showed that the expression of phoBR and aioBA were both induced by As(III) but were not induced in HAL1-phoR(931) and HAL1-▵phoB. Using 15 consensus Pho box sequences, a putative Pho box was found in the aioBA regulation region. PhoB was able to bind to the putative Pho box in vivo (bacterial one-hybrid detection) and in vitro (electrophoretic mobility gel shift assay), and an 18-bp binding sequence containing nine conserved bases were determined. This study provided the evidence that PhoBR regulates the expression of aioBA in Halomonas sp. HAL1 under low Pi condition. The new regulation model further implies the close metabolic connection between As and Pi. Frontiers Media S.A. 2015-09-09 /pmc/articles/PMC4563254/ /pubmed/26441863 http://dx.doi.org/10.3389/fmicb.2015.00923 Text en Copyright © 2015 Chen, Cao, Wei, Li, Li, Wang and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Chen, Fang
Cao, Yajing
Wei, Sha
Li, Yanzhi
Li, Xiangyang
Wang, Qian
Wang, Gejiao
Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1
title Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1
title_full Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1
title_fullStr Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1
title_full_unstemmed Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1
title_short Regulation of arsenite oxidation by the phosphate two-component system PhoBR in Halomonas sp. HAL1
title_sort regulation of arsenite oxidation by the phosphate two-component system phobr in halomonas sp. hal1
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563254/
https://www.ncbi.nlm.nih.gov/pubmed/26441863
http://dx.doi.org/10.3389/fmicb.2015.00923
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