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Expression, purification, crystallization and preliminary X-ray studies of the outer membrane efflux proteins OprM and OprN from Pseudomonas aeruginosa

Authors :
Isabelle Broutin
Marie-Bernard Lascombe
Arnaud Ducruix
Houssain Benabdelhak
Dimitri Lerouge
Xavier Moreel
Laboratoire de cristallographie et RMN biologiques (LCRB - UMR 8015)
Centre National de la Recherche Scientifique (CNRS)-Université Paris Descartes - Paris 5 (UPD5)
Axe cancer
Université Laval-CHUQ Research Center
Université Paris Descartes - Paris 5 (UPD5)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Université Laval [Québec] (ULaval)-CHUQ Research Center
Source :
Acta Crystallographica Section F: Structural Biology and Crystallization Communications, Acta Crystallographica Section F: Structural Biology and Crystallization Communications, 2005, 61 (3), pp.315-318. ⟨10.1107/S1744309105005014⟩
Publication Year :
2005
Publisher :
HAL CCSD, 2005.

Abstract

OprM and OprN belong to the outer membrane factor family proteins. These approximately 52 kDa proteins are part of the tripartite efflux pumps found in Pseudomonas aeruginosa and are responsible in part for the antibiotic resistance observed in these bacteria. Both proteins have been expressed in Escherichia coli as His-tag proteins and purified accordingly by affinity chromatography in the presence of n-octyl-beta-D-glucopyranoside detergent. OprM and OprN were crystallized using PEG 20 000/ammonium citrate and ammonium sulfate as precipitating agents, respectively. Crystals belong to space group C2, with unit-cell parameters a = 152.6, b = 87.9, c = 355.9 A, beta = 98.9 degrees and a = 151.3, b = 87.6, c = 356.5 A, beta = 98.1 degrees for OprM and OprN, respectively. Using the ESRF synchrotron-radiation source, OprM diffraction data extended to 3.4 A.

Details

Language :
English
Database :
OpenAIRE
Journal :
Acta Crystallographica Section F: Structural Biology and Crystallization Communications, Acta Crystallographica Section F: Structural Biology and Crystallization Communications, 2005, 61 (3), pp.315-318. ⟨10.1107/S1744309105005014⟩
Accession number :
edsair.doi.dedup.....6b39cafa8061298863e6fc9f95a43af9