A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ Transport

ATP-binding cassette transporters are ubiquitous in almost all organisms. The Escherichia coli genome is predicted to encode 69 ABC transporters. Eleven of the ABC transporters are presumed to be exporters, of which seven are possible drug export transporters. There has been minimal research on the...

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Main Authors: Zhenyue Feng, Defu Liu, Lizi Wang, Yanhong Wang, Zhongjing Zang, Zhenhua Liu, Baifen Song, Liwei Gu, Zhaowei Fan, Siyu Yang, Jing Chen, Yudong Cui
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-04-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2020.00556/full
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author Zhenyue Feng
Defu Liu
Lizi Wang
Yanhong Wang
Zhongjing Zang
Zhenhua Liu
Baifen Song
Liwei Gu
Zhaowei Fan
Siyu Yang
Jing Chen
Yudong Cui
author_facet Zhenyue Feng
Defu Liu
Lizi Wang
Yanhong Wang
Zhongjing Zang
Zhenhua Liu
Baifen Song
Liwei Gu
Zhaowei Fan
Siyu Yang
Jing Chen
Yudong Cui
author_sort Zhenyue Feng
collection DOAJ
description ATP-binding cassette transporters are ubiquitous in almost all organisms. The Escherichia coli genome is predicted to encode 69 ABC transporters. Eleven of the ABC transporters are presumed to be exporters, of which seven are possible drug export transporters. There has been minimal research on the function of YbhFSR, which is one of the putative drug resistance exporters. In this study, the ybhF gene of this transporter was characterized. Overexpression and knockout strains of ybhF were constructed. The ATPase activity of YbhF was studied using the malachite green assay, and the efflux abilities of knockout strains were demonstrated by using ethidium bromide (EB) as a substrate. The substrates of YbhFSR efflux, examined with the minimum inhibitory concentration (MIC), were determined to be tetracycline, oxytetracycline, chlortetracycline, doxycycline, EB, and Hoechst33342. Furthermore, tetracycline and EB efflux and accumulation experiments confirmed that the substrates of YbhFSR were tetracyclines and EB. The MIC assay and the fluorescence test results showed that tetracyclines are likely to be the major antibiotic substrate of YbhFSR. The existence of the signature NatA motif suggested that YbhFSR may also function as a Na+/H+ transporter. Overexpression of YbhF in E. coli KNabc lacking crucial Na+/H+ transporters conferred tolerance to NaCl, LiCl, and an alkaline pH. Together, the results showed that YbhFSR exhibited dual functions as a drug efflux pump and a Na+ (Li+)/H+ antiporter.
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spelling doaj.art-e291c0b9a10744c388e3c76a0f96653e2022-12-21T23:05:44ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-04-011110.3389/fmicb.2020.00556517634A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ TransportZhenyue FengDefu LiuLizi WangYanhong WangZhongjing ZangZhenhua LiuBaifen SongLiwei GuZhaowei FanSiyu YangJing ChenYudong CuiATP-binding cassette transporters are ubiquitous in almost all organisms. The Escherichia coli genome is predicted to encode 69 ABC transporters. Eleven of the ABC transporters are presumed to be exporters, of which seven are possible drug export transporters. There has been minimal research on the function of YbhFSR, which is one of the putative drug resistance exporters. In this study, the ybhF gene of this transporter was characterized. Overexpression and knockout strains of ybhF were constructed. The ATPase activity of YbhF was studied using the malachite green assay, and the efflux abilities of knockout strains were demonstrated by using ethidium bromide (EB) as a substrate. The substrates of YbhFSR efflux, examined with the minimum inhibitory concentration (MIC), were determined to be tetracycline, oxytetracycline, chlortetracycline, doxycycline, EB, and Hoechst33342. Furthermore, tetracycline and EB efflux and accumulation experiments confirmed that the substrates of YbhFSR were tetracyclines and EB. The MIC assay and the fluorescence test results showed that tetracyclines are likely to be the major antibiotic substrate of YbhFSR. The existence of the signature NatA motif suggested that YbhFSR may also function as a Na+/H+ transporter. Overexpression of YbhF in E. coli KNabc lacking crucial Na+/H+ transporters conferred tolerance to NaCl, LiCl, and an alkaline pH. Together, the results showed that YbhFSR exhibited dual functions as a drug efflux pump and a Na+ (Li+)/H+ antiporter.https://www.frontiersin.org/article/10.3389/fmicb.2020.00556/fullABC transportersYbhFSRYbhFtetracyclinessingle-drug efflux pumpNa+/H+ transporter
spellingShingle Zhenyue Feng
Defu Liu
Lizi Wang
Yanhong Wang
Zhongjing Zang
Zhenhua Liu
Baifen Song
Liwei Gu
Zhaowei Fan
Siyu Yang
Jing Chen
Yudong Cui
A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ Transport
Frontiers in Microbiology
ABC transporters
YbhFSR
YbhF
tetracyclines
single-drug efflux pump
Na+/H+ transporter
title A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ Transport
title_full A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ Transport
title_fullStr A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ Transport
title_full_unstemmed A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ Transport
title_short A Putative Efflux Transporter of the ABC Family, YbhFSR, in Escherichia coli Functions in Tetracycline Efflux and Na+(Li+)/H+ Transport
title_sort putative efflux transporter of the abc family ybhfsr in escherichia coli functions in tetracycline efflux and na li h transport
topic ABC transporters
YbhFSR
YbhF
tetracyclines
single-drug efflux pump
Na+/H+ transporter
url https://www.frontiersin.org/article/10.3389/fmicb.2020.00556/full
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