Protein-protein interactions that regulate the energy stress activation of σB in Bacillus subtilis.

  1. Lookup NU author(s)
  2. Dr Olivier Delumeau
  3. Professor Rick Lewis
Author(s)Delumeau O, Lewis RJ, Yudkin MD
Publication type Article
JournalJournal of Bacteriology
Year2002
Volume184
Issue20
Pages5583-5589
ISSN (print)0021-9193
ISSN (electronic)1098-5530
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
B is an alternative factor that controls the general stress response in Bacillus subtilis. In the absence of stress, B is negatively regulated by anti- factor RsbW. RsbW is also a protein kinase which can phosphorylate RsbV. When cells are stressed, RsbW binds to unphosphorylated RsbV, produced from the phosphorylated form of RsbV by two phosphatases (RsbU and RsbP) which are activated by stress. We now report the values of the Km for ATP and the Ki for ADP of RsbW (0.9 and 0.19 mM, respectively), which reinforce the idea that the kinase activity of RsbW is directly regulated in vivo by the ratio of these nucleotides. RsbW, purified as a dimer, forms complexes with RsbV and B with different stoichiometries, i.e., RsbW2-RsbV2 and RsbW2-B1. As determined by surface plasmon resonance, the dissociation constants of the RsbW-RsbV and RsbW-B interactions were found to be similar (63 and 92 nM, respectively). Nonetheless, an analysis of the complexes by nondenaturing polyacrylamide gel electrophoresis in competition assays suggested that the affinity of RsbW2 for RsbV is much higher than that for B. The intracellular concentrations of RsbV, RsbW (as a monomer), and B measured before stress were similar (1.5, 2.6, and 0.9 µM, respectively). After ethanol stress they all increased. The increase was greatest for RsbV, whose concentration reached 13 µM, while those of RsbW (as a monomer) and B reached 11.8 and 4.9 µM, respectively. We conclude that the higher affinity of RsbW for RsbV than for B, rather than a difference in the concentrations of RsbV and B, is the driving force that is responsible for the switch of RsbW to unphosphorylated RsbV.
PublisherAmerican Society for Microbiology
URLhttp://dx.doi.org/10.1128/JB.184.20.5583-5589.2002
DOI10.1128/JB.184.20.5583-5589.2002
Actions    Link to this publication