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Journal of Bacteriology, March 2001, p. 1843-1852, Vol. 183, No. 6
Institute of Medical Microbiology, University
of Zürich, CH-8028 Zürich,
Switzerland,1 and Institute of
Microbiology and Molecular Biology, Ernst-Moritz-Arndt University,
D-17487 Greifswald, Germany2
Received 6 September 2000/Accepted 14 December 2000
Derivatives of the widely used laboratory strain
Staphylococcus aureus NCTC8325, which are natural
rsbU mutants, were shown to be unable to produce RsbU, a
positive regulator of the alternative sigma factor
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.6.1843-1852.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
B Activity Depends on RsbU in
Staphylococcus aureus
B.
The lack of RsbU prevented the heat-dependent production of
B-controlled transcripts and resulted in reduced
H2O2 and UV tolerance, enhanced alpha-hemolysin
activity, and the inability to produce the alkaline shock protein
Asp23. After 48 h of growth, rsbU mutant strains
failed to accumulate staphyloxanthin, the major stationary-phase carotenoid. Transcription of Asp23 was found to be exclusively controlled by
B, making it an excellent target for the
study of
B activity in S. aureus. Reporter
gene experiments, using the firefly luciferase gene (luc+)
fused to the
B-dependent promoter(s) of
asp23, revealed that
B is almost inactive in
8325 derivatives. cis complementation of the 8325 derivative BB255 with the wild-type rsbU gene from strain COL produced the rsbU+ derivative GP268, a
strain possessing a
B activity profile comparable to
that of the rsbU+ wild-type strain Newman. In
GP268, the heat inducibility of
B-dependent genes, Asp23
production, alpha-hemolysin activity, pigmentation, and susceptibility
to H2O2 were restored to the levels observed in
strain Newman, clearly demonstrating that RsbU is needed for activation
of
B in S. aureus.
*
Corresponding author. Mailing address: Institute of
Medical Microbiology, University of Zürich, Gloriastr. 32, Postfach, CH-8028 Zürich, Switzerland. Phone: 41 1 634 26 70. Fax: 41 1 634 49 06. E-mail: bischoff{at}immv.unizh.ch.
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