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Journal of Bacteriology, November 2008, p. 7141-7146, Vol. 190, No. 21
0021-9193/08/$08.00+0 doi:10.1128/JB.00676-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Université Paris-Sud, UMR 8619, Institut de Biochimie et de Biophysique Moléculaire et Cellulaire, Orsay, France,1 CNRS, UMR 8619, Laboratoire des Enveloppes Bactériennes et Antibiotiques, Orsay, France2
Received 14 May 2008/ Accepted 2 August 2008
To date, the structural and functional characterization of proteins belonging to the polyprenyl-phosphate N-acetylhexosamine-1-phosphate transferase superfamily has been relentlessly held back by problems encountered with their overexpression and purification. In the present work and for the first time, the integral membrane protein WecA that catalyzes the transfer of the GlcNAc-1-phosphate moiety from UDP-GlcNAc onto the carrier lipid undecaprenyl phosphate, yielding undecaprenyl-pyrophosphoryl-GlcNAc, the lipid intermediate involved in the synthesis of various bacterial cell envelope components, was overproduced and purified to near homogeneity in milligram quantities. An enzymatic assay was developed, and the kinetic parameters of WecA as well as the effects of pH, salts, cations, detergents, and temperature on the enzyme activity were determined. A minimal length of 35 carbons was required for the lipid substrate, and tunicamycin was shown to inhibit the enzyme at submicromolar concentrations.
Published ahead of print on 22 August 2008.
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