Journal of Bacteriology, December 2000, p. 6592-6597, Vol. 182, No. 23
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Microbiology Department, Brigham Young University, Provo, Utah 84602-5253
Received 17 July 2000/Accepted 18 September 2000
PhoB is the response regulator of the Pho regulon. It is composed
of two distinct domains, an N-terminal receiver domain and a C-terminal
output domain that binds DNA and interacts with
70 to
activate transcription of the Pho regulon. Phosphorylation of the
receiver domain is required for activation of the protein. The
mechanism of activation by phosphorylation has not yet been determined.
To better understand the function of the receiver domain in controlling
the activity of the output domain, a direct comparison was made between
unphosphorylated PhoB and its solitary DNA-binding domain
(PhoBDBD) for DNA binding and transcriptional activation.
Using fluorescence anisotropy, it was found that PhoBDBD
bound to the pho box with an affinity seven times greater
than that of unphosphorylated PhoB. It was also found that
PhoBDBD was better able to activate transcription than the
full-length, unmodified protein. We conclude that the unphosphorylated
receiver domain of PhoB silences the activity of its output domain.
These results suggest that upon phosphorylation of the receiver domain of PhoB, the inhibition placed upon the output domain is relieved by a
conformational change that alters interactions between the unphosphorylated receiver domain and the output domain.
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