THE K-EFFLUX SYSTEM, KEFC, IN ESCHERICHIA-COLI - GENETIC-EVIDENCE FOROLIGOMERIC STRUCTURE()

Citation
Rm. Douglas et al., THE K-EFFLUX SYSTEM, KEFC, IN ESCHERICHIA-COLI - GENETIC-EVIDENCE FOROLIGOMERIC STRUCTURE(), Molecular membrane biology, 11(1), 1994, pp. 55-61
Citations number
30
Categorie Soggetti
Cytology & Histology",Biology
Journal title
ISSN journal
09687688
Volume
11
Issue
1
Year of publication
1994
Pages
55 - 61
Database
ISI
SICI code
0968-7688(1994)11:1<55:TKSKIE>2.0.ZU;2-Y
Abstract
KefC is a glutathione-gated K+-efflux system that is widespread in Gra m negative bacteria and which plays a role in the protection of cells from the toxic effects of electrophilic reagents, such as N-ethylmalei mide (NEM). The KefC gene from Escherichia coli has been cloned and th e DNA sequenced. A number of kefC mutants that affect K+ retention by the KefC system have been isolated and all retain activation by NEM. C loned kefC was found to suppress the phenotype of two such mutants kef C121 and kefC103. Analysis of this phenomenon has shown that suppressi on is specific to the KefC system, but that cloned kefC from Klebsiell a and Erwinia can also mediate suppression of the mutant phenotype. Pl asmid constructs of the E. coli gene in which expression of the cloned gene was diminished showed reduced ability to suppress the mutant phe notype. KefC' - 'LacZ hybrid proteins were inserted in the membrane bu t did not suppress the mutant phenotype. cloned kefC did not suppress a mutant kefB allele that exhibited a similar phenotype to the kefC121 allele. These data suggest that suppression is unlikely to arise from exclusion of the mutant form of the protein from the membrane. Furthe rmore, NEM-activated K+ efflux from a strain carrying both the mutant and cloned wild-type alleles was faster than when either allele was pr esent in cells alone, suggesting that both forms of the protein are in serted into the membrane. These data are discussed in terms of a model for the KefC protein in which the protein is composed of one or more identical subunits that interact in the membrane.