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Journal of Bacteriology, March 2007, p. 1531-1541, Vol. 189, No. 5
0021-9193/07/$08.00+0     doi:10.1128/JB.01649-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Isolation and Characterization of Dominant Mutations in the Bacillus subtilis Stressosome Components RsbR and RsbS{triangledown}

Adam Reeves and W. G. Haldenwang*

Department of Microbiology and Immunology—MC7758, University of Texas Health Science Center, San Antonio, Texas 78229-3900

Received 24 October 2006/ Accepted 29 November 2006

The general stress response of Bacillus subtilis is controlled by the activity state of the {sigma}B transcription factor. Physical stress is communicated to {sigma}B via a large-molecular-mass (>106-Da) structure (the stressosome) formed by one or more members of a family of homologous proteins (RsbR, YkoB, YojH, YqhA). The positive regulator (RsbT) of the {sigma}B stress induction pathway is incorporated into the complex bound to an inhibitor protein (RsbS). Exposure to stress empowers an RsbT-dependent phosphorylation of RsbR and RsbS, with the subsequent release of RsbT to activate downstream processes. The mechanism by which stress initiates these reactions is unknown. In an attempt to identify changes in stressosome components that could lead to {sigma}B activation, a DNA segment encoding these proteins was mutagenized and placed into B. subtilis to create a merodiploid strain for these genes. Eight mutations that allowed heightened {sigma}B activity in the presence of their wild-type counterparts were isolated. Two of the mutations are missense changes in rsbR, and six are amino acid changes in rsbS. Additional experiments suggested that both of the rsbR mutations and three of the rsbS mutations likely enhance {sigma}B activity by elevating the level of RsbS phosphorylation. All of the mutations were found to be dominant over wild-type alleles only when they are cotranscribed within an rsbR rsbS rsbT operon. The data suggest that changes in RsbR can initiate the downstream events that lead to {sigma}B activation and that RsbR, RsbS, and RsbT likely interact with each other concomitantly with their synthesis.

* Corresponding author. Mailing address: Department of Microbiology and Immunology—MC7758, University of Texas Health Science Center, San Antonio, TX 78229-3900. Phone: (210) 567-3957. Fax: (210) 567-6612. E-mail: haldenwang{at}uthscsa.edu.

{triangledown} Published ahead of print on 8 December 2006.

Journal of Bacteriology, March 2007, p. 1531-1541, Vol. 189, No. 5
0021-9193/07/$08.00+0     doi:10.1128/JB.01649-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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