Literature DB >> 12578981

The Escherichia coli multidrug transporter MdfA catalyzes both electrogenic and electroneutral transport reactions.

Oded Lewinson1, Julia Adler, Gerrit J Poelarends, Piotr Mazurkiewicz, Arnold J M Driessen, Eitan Bibi.   

Abstract

The resistance of cells to many drugs simultaneously (multidrug resistance) often involves the expression of membrane transporters (Mdrs); each recognizes and expels a broad spectrum of chemically unrelated drugs from the cell. The Escherichia coli Mdr transporter MdfA is able to transport differentially charged substrates in exchange for protons. This includes neutral compounds, namely chloramphenicol and thiamphenicol, and lipophilic cations such as tetraphenylphosphonium and ethidium. Here we show that the chloramphenicol and thiamphenicol transport reactions are electrogenic, whereas the transport of several monovalent cationic substrates is electroneutral. Therefore, unlike with positively charged substrates, the transmembrane electrical potential (negative inside) constitutes a major part of the driving force for the transport of electroneutral substrates by MdfA. These results demonstrate an unprecedented ability of a single secondary transporter to catalyze discrete transport reactions that differ in their electrogenicity and are governed by different components of the proton motive force.

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Year:  2003        PMID: 12578981      PMCID: PMC149890          DOI: 10.1073/pnas.0435544100

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  24 in total

Review 1.  MdfA, an interesting model protein for studying multidrug transport.

Authors:  E Bibi; J Adler; O Lewinson; R Edgar
Journal:  J Mol Microbiol Biotechnol       Date:  2001-04

2.  A broad-specificity multidrug efflux pump requiring a pair of homologous SMR-type proteins.

Authors:  D L Jack; M L Storms; J H Tchieu; I T Paulsen; M H Saier
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

Review 3.  Multiple antibiotic resistance and efflux.

Authors:  H Nikaido
Journal:  Curr Opin Microbiol       Date:  1998-10       Impact factor: 7.934

Review 4.  Multidrug resistance mechanisms: drug efflux across two membranes.

Authors:  H I Zgurskaya; H Nikaido
Journal:  Mol Microbiol       Date:  2000-07       Impact factor: 3.501

5.  Functional expression of mouse Mdr1 in an outer membrane permeability mutant of Escherichia coli.

Authors:  O Béjà; E Bibi
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-11       Impact factor: 11.205

6.  Detergent-mediated reconstitution of membrane proteins.

Authors:  J Knol; K Sjollema; B Poolman
Journal:  Biochemistry       Date:  1998-11-17       Impact factor: 3.162

Review 7.  Reconstitution of membrane proteins into liposomes: application to energy-transducing membrane proteins.

Authors:  J L Rigaud; B Pitard; D Levy
Journal:  Biochim Biophys Acta       Date:  1995-10-10

8.  The secondary multidrug transporter LmrP contains multiple drug interaction sites.

Authors:  M Putman; L A Koole; H W van Veen; W N Konings
Journal:  Biochemistry       Date:  1999-10-19       Impact factor: 3.162

9.  A single membrane-embedded negative charge is critical for recognizing positively charged drugs by the Escherichia coli multidrug resistance protein MdfA.

Authors:  R Edgar; E Bibi
Journal:  EMBO J       Date:  1999-02-15       Impact factor: 11.598

10.  Evidence for chloramphenicol/H+ antiport in Cmr (MdfA) system of Escherichia coli and properties of the antiporter.

Authors:  T Mine; Y Morita; A Kataoka; T Mizushima; T Tsuchiya
Journal:  J Biochem       Date:  1998-07       Impact factor: 3.387

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  35 in total

Review 1.  Structure and function of efflux pumps that confer resistance to drugs.

Authors:  M Ines Borges-Walmsley; Kenneth S McKeegan; Adrian R Walmsley
Journal:  Biochem J       Date:  2003-12-01       Impact factor: 3.857

2.  Substrate-bound structure of the E. coli multidrug resistance transporter MdfA.

Authors:  Jie Heng; Yan Zhao; Ming Liu; Yue Liu; Junping Fan; Xianping Wang; Yongfang Zhao; Xuejun C Zhang
Journal:  Cell Res       Date:  2015-08-04       Impact factor: 25.617

Review 3.  Energy coupling mechanisms of MFS transporters.

Authors:  Xuejun C Zhang; Yan Zhao; Jie Heng; Daohua Jiang
Journal:  Protein Sci       Date:  2015-09-18       Impact factor: 6.725

4.  Characterization of bacterial drug antiporters homologous to mammalian neurotransmitter transporters.

Authors:  Eyal Vardy; Sonia Steiner-Mordoch; Shimon Schuldiner
Journal:  J Bacteriol       Date:  2005-11       Impact factor: 3.490

5.  No single irreplaceable acidic residues in the Escherichia coli secondary multidrug transporter MdfA.

Authors:  Nadejda Sigal; Shahar Molshanski-Mor; Eitan Bibi
Journal:  J Bacteriol       Date:  2006-08       Impact factor: 3.490

6.  The secondary multidrug/proton antiporter MdfA tolerates displacements of an essential negatively charged side chain.

Authors:  Nadejda Sigal; Nir Fluman; Shira Siemion; Eitan Bibi
Journal:  J Biol Chem       Date:  2009-01-07       Impact factor: 5.157

Review 7.  The challenge of efflux-mediated antibiotic resistance in Gram-negative bacteria.

Authors:  Xian-Zhi Li; Patrick Plésiat; Hiroshi Nikaido
Journal:  Clin Microbiol Rev       Date:  2015-04       Impact factor: 26.132

Review 8.  New functions for the ancient DedA membrane protein family.

Authors:  William T Doerrler; Rakesh Sikdar; Sujeet Kumar; Lisa A Boughner
Journal:  J Bacteriol       Date:  2012-10-19       Impact factor: 3.490

9.  Manipulating the drug/proton antiport stoichiometry of the secondary multidrug transporter MdfA.

Authors:  Osnat Tirosh; Nadejda Sigal; Amir Gelman; Nadav Sahar; Nir Fluman; Shira Siemion; Eitan Bibi
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-16       Impact factor: 11.205

10.  Escherichia coli YqjA, a Member of the Conserved DedA/Tvp38 Membrane Protein Family, Is a Putative Osmosensing Transporter Required for Growth at Alkaline pH.

Authors:  Sujeet Kumar; William T Doerrler
Journal:  J Bacteriol       Date:  2015-04-27       Impact factor: 3.490

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