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Journal of Bacteriology, May 2008, p. 3786-3790, Vol. 190, No. 10
0021-9193/08/$08.00+0 doi:10.1128/JB.01994-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Kassem Hamze,1
Didier Blanot,2
Claude Frehel,3
Rut Carballido-Lopez,4
Barry I. Holland,1
Jean van Heijenoort,2 and
Simone J. Séror1*
Université Paris-Sud 11, Institut de Génétique et Microbiologie, CNRS UMR 8621, Bâtiment 409, 91405 Orsay Cedex, France,1 Université Paris-Sud 11, Institut de Biochimie et Biophysique Moléculaire et Cellulaire, CNRS UMR 8619, Bâtiment 430, 91405 Orsay Cedex, France,2 Institut National de la Santé et de la Recherche Médicale, U-570, CHU Necker, Enfants Malades, 156 Rue de Vaugirard, 75730 Paris Cedex 15, France,3 Institut National de la Recherche Agronomique, UR 895, Génétique Microbienne, Dynamique du Génome-Génomique, Domaine de Vilvert, 78352 Jouy-en-Josas Cedex, France4
Received 21 December 2007/ Accepted 4 March 2008
Depletion of the Bacillus subtilis GTPase CpgA produces abnormal cell shapes, nonuniform deposition of cell wall, and five- to sixfold accumulation of peptidoglycan precursors. Nevertheless, the inherent structure of the cell wall appeared mostly unchanged. The results are consistent with CpgA being involved in coordinating normal peptidoglycan deposition.
Published ahead of print on 14 March 2008.
Present address: Division of Infectious Disease, Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115.
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