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A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1

Cesium ion (Cs(+)) resistance has been reported in bacteria but is poorly understood as reports on Cs(+)-resistant bacteria have been limited. We previously reported a novel Cs(+)/H(+) antiporter CshA implicated in Cs(+)-resistance in Microbacterium sp. TS-1. The present study used the same screenin...

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Autores principales: Ishida, Yoshiki, Koretsune, Takahiro, Ishiuchi, Eri, Teshima, Miyu, Ito, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995610/
https://www.ncbi.nlm.nih.gov/pubmed/36910217
http://dx.doi.org/10.3389/fmicb.2023.1136514
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author Ishida, Yoshiki
Koretsune, Takahiro
Ishiuchi, Eri
Teshima, Miyu
Ito, Masahiro
author_facet Ishida, Yoshiki
Koretsune, Takahiro
Ishiuchi, Eri
Teshima, Miyu
Ito, Masahiro
author_sort Ishida, Yoshiki
collection PubMed
description Cesium ion (Cs(+)) resistance has been reported in bacteria but is poorly understood as reports on Cs(+)-resistant bacteria have been limited. We previously reported a novel Cs(+)/H(+) antiporter CshA implicated in Cs(+)-resistance in Microbacterium sp. TS-1. The present study used the same screening method to isolate novel Cs(+)-sensitive mutants and their revertants from TS-1. A comparative mutation site analysis using whole-genome sequencing revealed that MTS1_03028 encodes the Mg(2+) transporter MgtE and is a candidate Cs(+) resistance-related gene. We performed a bioinformatic analysis of MTS1_03028 and complementation experiments on Cs(+) resistance in the TS-1 MTS1_03028 mutants Mut5 and Mut7 as well as Escherichia coli expressing MTS1_03028 in the presence of Mg(2+). We established the role of MgtE in Cs(+) resistance through a functional analysis of TS-1. Enhancing Mg(2+) transport by expression of MTS_03028 conferred increased Cs(+) resistance. When this strain was exposed to Cs(+) concentrations exceeding 200 mM, CshA consistently lowered the intracellular Cs(+) concentration. To our knowledge, the present study is the first to clarify the mechanism of Cs(+) resistance in certain bacteria. The study findings offer important insights into the mechanism of bacterial resistance to excess Cs(+) in the environment, suggesting the potential for bioremediation in high Cs-contaminated areas.
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spelling pubmed-99956102023-03-10 A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1 Ishida, Yoshiki Koretsune, Takahiro Ishiuchi, Eri Teshima, Miyu Ito, Masahiro Front Microbiol Microbiology Cesium ion (Cs(+)) resistance has been reported in bacteria but is poorly understood as reports on Cs(+)-resistant bacteria have been limited. We previously reported a novel Cs(+)/H(+) antiporter CshA implicated in Cs(+)-resistance in Microbacterium sp. TS-1. The present study used the same screening method to isolate novel Cs(+)-sensitive mutants and their revertants from TS-1. A comparative mutation site analysis using whole-genome sequencing revealed that MTS1_03028 encodes the Mg(2+) transporter MgtE and is a candidate Cs(+) resistance-related gene. We performed a bioinformatic analysis of MTS1_03028 and complementation experiments on Cs(+) resistance in the TS-1 MTS1_03028 mutants Mut5 and Mut7 as well as Escherichia coli expressing MTS1_03028 in the presence of Mg(2+). We established the role of MgtE in Cs(+) resistance through a functional analysis of TS-1. Enhancing Mg(2+) transport by expression of MTS_03028 conferred increased Cs(+) resistance. When this strain was exposed to Cs(+) concentrations exceeding 200 mM, CshA consistently lowered the intracellular Cs(+) concentration. To our knowledge, the present study is the first to clarify the mechanism of Cs(+) resistance in certain bacteria. The study findings offer important insights into the mechanism of bacterial resistance to excess Cs(+) in the environment, suggesting the potential for bioremediation in high Cs-contaminated areas. Frontiers Media S.A. 2023-02-23 /pmc/articles/PMC9995610/ /pubmed/36910217 http://dx.doi.org/10.3389/fmicb.2023.1136514 Text en Copyright © 2023 Ishida, Koretsune, Ishiuchi, Teshima and Ito. https://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) and the copyright owner(s) 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
Ishida, Yoshiki
Koretsune, Takahiro
Ishiuchi, Eri
Teshima, Miyu
Ito, Masahiro
A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1
title A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1
title_full A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1
title_fullStr A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1
title_full_unstemmed A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1
title_short A magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium Microbacterium sp. TS-1
title_sort magnesium transporter is involved in the cesium ion resistance of the high-concentration cesium ion-resistant bacterium microbacterium sp. ts-1
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995610/
https://www.ncbi.nlm.nih.gov/pubmed/36910217
http://dx.doi.org/10.3389/fmicb.2023.1136514
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