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Expression, refolding, crystallization and...
Journal article

Expression, refolding, crystallization and preliminary X-ray analysis of Pseudomonas aeruginosa AlgE

Abstract

AlgE is an outer membrane protein present in alginate-producing (mucoid) Pseudomonas aeruginosa. AlgE has been overexpressed in insoluble inclusion bodies, purified under denaturing conditions and refolded in a buffer containing decyl beta-D-maltopyranoside. Purified refolded AlgE was detergent-exchanged into n-octyl tetraoxyethylene and diffraction-quality crystals were grown using the hanging-drop vapor-diffusion method. The crystals grew as small hexagons with unit-cell parameters a = 98.8, b = 156.8, c = 90.4 A, alpha = beta = gamma = 90.0 degrees . The crystals exhibited the symmetry of space group C222 and diffracted to a minimum d-spacing of 3.0 A. On the basis of the Matthews coefficient (V(M) = 3.28 A(3) Da(-1)), one molecule is estimated to be present in the asymmetric unit.

Authors

Whitney JCC; Neculai AM; Ohman DE; Howell PL

Journal

Acta Crystallographica Section F: Structural Biology Communications, Vol. 65, No. 5, pp. 463–466

Publisher

International Union of Crystallography (IUCr)

Publication Date

May 1, 2009

DOI

10.1107/s174430910901094x

ISSN

2053-230X

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