The Salmonella enterica sv. Typhimurium smvA, yddG and ompD (porin) genes are required for the efficient efflux of methyl viologen

Summary In Gram‐negative bacteria, a subset of inner membrane proteins in the major facilitator superfamily (MFS) acts as efflux pumps to decrease the intracellular concentrations of multiple toxic substrates and confers multidrug resistance. The Salmonella enterica sv. Typhimurium smvA gene encodes...

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Veröffentlicht in:Molecular microbiology 2002-11, Vol.46 (3), p.687-698
Hauptverfasser: Santiviago, Carlos A., Fuentes, Juan A., Bueno, Susan M., Trombert, A. Nicole, Hildago, Alejandro A., Socias, L. Teresa, Youderian, Philip, Mora, Guido C.
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container_end_page 698
container_issue 3
container_start_page 687
container_title Molecular microbiology
container_volume 46
creator Santiviago, Carlos A.
Fuentes, Juan A.
Bueno, Susan M.
Trombert, A. Nicole
Hildago, Alejandro A.
Socias, L. Teresa
Youderian, Philip
Mora, Guido C.
description Summary In Gram‐negative bacteria, a subset of inner membrane proteins in the major facilitator superfamily (MFS) acts as efflux pumps to decrease the intracellular concentrations of multiple toxic substrates and confers multidrug resistance. The Salmonella enterica sv. Typhimurium smvA gene encodes a product predicted to be an MFS protein most similar to QacA of Staphylococcus aureus. Like mutations in qacA, mutations in smvA confer increased sensitivity to methyl viologen (MV). Mutations in the adjacent ompD (porin) and yddG (drug/metabolite transporter) genes also confer increased sensitivity to MV, and mutations in smvA are epistatic to mutations in ompD or yddG for this phenotype. YddG and OmpD probably comprise a second efflux pump in which the OmpD porin acts as an outer membrane channel (OMC) protein for the efflux of MV and functions independently of the SmvA pump. In support of this idea, the pump dependent on YddG and OmpD has a different substrate specificity from the pump dependent on SmvA. Mutations in tolC, which encodes an OMC protein, confer increased resistance to MV. TolC apparently facilitates the import of MV, and a subset of OMC proteins including the OmpD porin and TolC may facilitate both import and export of distinct subsets of toxic substrates.
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Typhimurium smvA, yddG and ompD (porin) genes are required for the efficient efflux of methyl viologen</title><source>MEDLINE</source><source>Wiley Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Wiley Online Library (Open Access Collection)</source><source>Free Full-Text Journals in Chemistry</source><creator>Santiviago, Carlos A. ; Fuentes, Juan A. ; Bueno, Susan M. ; Trombert, A. Nicole ; Hildago, Alejandro A. ; Socias, L. Teresa ; Youderian, Philip ; Mora, Guido C.</creator><creatorcontrib>Santiviago, Carlos A. ; Fuentes, Juan A. ; Bueno, Susan M. ; Trombert, A. Nicole ; Hildago, Alejandro A. ; Socias, L. Teresa ; Youderian, Philip ; Mora, Guido C.</creatorcontrib><description>Summary In Gram‐negative bacteria, a subset of inner membrane proteins in the major facilitator superfamily (MFS) acts as efflux pumps to decrease the intracellular concentrations of multiple toxic substrates and confers multidrug resistance. The Salmonella enterica sv. Typhimurium smvA gene encodes a product predicted to be an MFS protein most similar to QacA of Staphylococcus aureus. Like mutations in qacA, mutations in smvA confer increased sensitivity to methyl viologen (MV). Mutations in the adjacent ompD (porin) and yddG (drug/metabolite transporter) genes also confer increased sensitivity to MV, and mutations in smvA are epistatic to mutations in ompD or yddG for this phenotype. YddG and OmpD probably comprise a second efflux pump in which the OmpD porin acts as an outer membrane channel (OMC) protein for the efflux of MV and functions independently of the SmvA pump. In support of this idea, the pump dependent on YddG and OmpD has a different substrate specificity from the pump dependent on SmvA. Mutations in tolC, which encodes an OMC protein, confer increased resistance to MV. TolC apparently facilitates the import of MV, and a subset of OMC proteins including the OmpD porin and TolC may facilitate both import and export of distinct subsets of toxic substrates.</description><identifier>ISSN: 0950-382X</identifier><identifier>EISSN: 1365-2958</identifier><identifier>DOI: 10.1046/j.1365-2958.2002.03204.x</identifier><identifier>PMID: 12410826</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Amino Acid Sequence ; Cloning, Molecular ; Drug Resistance, Bacterial ; Herbicides - metabolism ; Herbicides - pharmacology ; Microbial Sensitivity Tests ; Molecular Sequence Data ; Mutation ; Paraquat - metabolism ; Paraquat - pharmacology ; Porins - chemistry ; Porins - genetics ; Porins - metabolism ; Salmonella typhimurium - drug effects ; Salmonella typhimurium - genetics ; Salmonella typhimurium - metabolism ; Substrate Specificity</subject><ispartof>Molecular microbiology, 2002-11, Vol.46 (3), p.687-698</ispartof><rights>Copyright Blackwell Scientific Publications Ltd. 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Mutations in the adjacent ompD (porin) and yddG (drug/metabolite transporter) genes also confer increased sensitivity to MV, and mutations in smvA are epistatic to mutations in ompD or yddG for this phenotype. YddG and OmpD probably comprise a second efflux pump in which the OmpD porin acts as an outer membrane channel (OMC) protein for the efflux of MV and functions independently of the SmvA pump. In support of this idea, the pump dependent on YddG and OmpD has a different substrate specificity from the pump dependent on SmvA. Mutations in tolC, which encodes an OMC protein, confer increased resistance to MV. TolC apparently facilitates the import of MV, and a subset of OMC proteins including the OmpD porin and TolC may facilitate both import and export of distinct subsets of toxic substrates.</description><subject>Amino Acid Sequence</subject><subject>Cloning, Molecular</subject><subject>Drug Resistance, Bacterial</subject><subject>Herbicides - metabolism</subject><subject>Herbicides - pharmacology</subject><subject>Microbial Sensitivity Tests</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Paraquat - metabolism</subject><subject>Paraquat - pharmacology</subject><subject>Porins - chemistry</subject><subject>Porins - genetics</subject><subject>Porins - metabolism</subject><subject>Salmonella typhimurium - drug effects</subject><subject>Salmonella typhimurium - genetics</subject><subject>Salmonella typhimurium - metabolism</subject><subject>Substrate Specificity</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAURi0EokPhFZDFAoHEBP_Exl50URUolVqxYJDYWU58w3iUxKk9GSZbnrwOM6JSV135Sj7fJ18fhDAlBSWl_LgpKJdiybRQBSOEFYQzUhb7J2jx_-IpWhAtyJIr9usEvUhpQwjlRPLn6ISykhLF5AL9Xa0B_7BtF3poW4uh30L0tcVpV-DVNKx9N0Y_djh1u_MPeHLuEtve4dANn_G7IUTfv8e_oYeEbQQc4Xb0ERxuQsTbXA1N42ufW-epHfc4NLiD7Xpq8c6HNuToS_SssW2CV8fzFP38-mV18W15_f3y6uL8elkLrsu8h2bMOapBqwqqRlvFSQW11LyurLK8ZFSIygkhiFba5VRlrWKfpOOSlBU_RW8PvUMMtyOkrel8quetewhjMlRJlj9OZvDNA3ATxtjntxmqpaCSEZ0hdYDqGFKK0Jgh-s7GyVBiZklmY2YXZnZhZknmnySzz9HXx_6x6sDdB49WMnB2AP74FqZHF5ubm6t54neNLaBo</recordid><startdate>200211</startdate><enddate>200211</enddate><creator>Santiviago, Carlos A.</creator><creator>Fuentes, Juan A.</creator><creator>Bueno, Susan M.</creator><creator>Trombert, A. 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Nicole</creatorcontrib><creatorcontrib>Hildago, Alejandro A.</creatorcontrib><creatorcontrib>Socias, L. Teresa</creatorcontrib><creatorcontrib>Youderian, Philip</creatorcontrib><creatorcontrib>Mora, Guido C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santiviago, Carlos A.</au><au>Fuentes, Juan A.</au><au>Bueno, Susan M.</au><au>Trombert, A. Nicole</au><au>Hildago, Alejandro A.</au><au>Socias, L. Teresa</au><au>Youderian, Philip</au><au>Mora, Guido C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Salmonella enterica sv. Typhimurium smvA, yddG and ompD (porin) genes are required for the efficient efflux of methyl viologen</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>2002-11</date><risdate>2002</risdate><volume>46</volume><issue>3</issue><spage>687</spage><epage>698</epage><pages>687-698</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Summary In Gram‐negative bacteria, a subset of inner membrane proteins in the major facilitator superfamily (MFS) acts as efflux pumps to decrease the intracellular concentrations of multiple toxic substrates and confers multidrug resistance. The Salmonella enterica sv. Typhimurium smvA gene encodes a product predicted to be an MFS protein most similar to QacA of Staphylococcus aureus. Like mutations in qacA, mutations in smvA confer increased sensitivity to methyl viologen (MV). Mutations in the adjacent ompD (porin) and yddG (drug/metabolite transporter) genes also confer increased sensitivity to MV, and mutations in smvA are epistatic to mutations in ompD or yddG for this phenotype. YddG and OmpD probably comprise a second efflux pump in which the OmpD porin acts as an outer membrane channel (OMC) protein for the efflux of MV and functions independently of the SmvA pump. In support of this idea, the pump dependent on YddG and OmpD has a different substrate specificity from the pump dependent on SmvA. Mutations in tolC, which encodes an OMC protein, confer increased resistance to MV. TolC apparently facilitates the import of MV, and a subset of OMC proteins including the OmpD porin and TolC may facilitate both import and export of distinct subsets of toxic substrates.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>12410826</pmid><doi>10.1046/j.1365-2958.2002.03204.x</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Online Library (Open Access Collection); Free Full-Text Journals in Chemistry
subjects Amino Acid Sequence
Cloning, Molecular
Drug Resistance, Bacterial
Herbicides - metabolism
Herbicides - pharmacology
Microbial Sensitivity Tests
Molecular Sequence Data
Mutation
Paraquat - metabolism
Paraquat - pharmacology
Porins - chemistry
Porins - genetics
Porins - metabolism
Salmonella typhimurium - drug effects
Salmonella typhimurium - genetics
Salmonella typhimurium - metabolism
Substrate Specificity
title The Salmonella enterica sv. Typhimurium smvA, yddG and ompD (porin) genes are required for the efficient efflux of methyl viologen
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