The porin RafY encoded by the raffinose plasmid pRSD2 of Escherichia coli forms a general diffusion pore and not a carbohydrate-specific porin

Autor(en): Andersen, C
Krones, D
Ulmke, C
Schmid, K
Benz, R
Stichwörter: BACTERIAL; BINDING-PROTEIN; Biochemistry & Molecular Biology; carbohydrate specificity; CHANNELS; enteric bacteria; LAMBDA-RECEPTOR; lipid bilayer membrane; LIPID BILAYER-MEMBRANES; MATRIX PROTEIN PORIN; MEDIATED SUCROSE METABOLISM; OUTER-MEMBRANE; PSEUDOMONAS-AERUGINOSA; raffinose transport; RafY channel; SALMONELLA-TYPHIMURIUM
Erscheinungsdatum: 1998
Herausgeber: SPRINGER VERLAG
Journal: EUROPEAN JOURNAL OF BIOCHEMISTRY
Volumen: 254
Ausgabe: 3
Startseite: 679
Seitenende: 684
Zusammenfassung: 
The gene rafY from the plasmid pRSD2, which enables Escherichia coli to grow on raffinose, was transferred into expression plasmid pUSL77. The protein was expressed in the porin-deficient Escherichia coli strain KS26 and was isolated and purified to homogeneity. The pure protein was reconstituted into lipid bilayer membranes. It formed an ion-permeable channel with a single-channel conductance of 2.9 nS of the open state in 1 M KCl, which is approximately twice of that of the general diffusion pores OmpF and OmpC of E. coli outer membrane. At lower pH the channel exhibited rapid flickering between three substates of the open channel. The RafY channel appears to be wide and water filled and has a small selectivity for cations over anions. Although RafY is part of an uptake and fermentation system for raffinose it does not contain a binding site for carbohydrates. Our results suggest that RafY is a general diffusion pore with a diameter, larger than that of the general diffusion porins OmpF and OmpC, that allows the diffusion of high-molecular-mass carbohydrates through the outer membrane.
ISSN: 00142956
DOI: 10.1046/j.1432-1327.1998.2540679.x

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