Journal of Bacteriology, August 2001, p. 4932-4937, Vol. 183, No. 16
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.16.4932-4937.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Department of Molecular Biology, IRIS Chiron S.p.A., 53100 Siena,1 and Department of Biology, University of Bologna, 40126 Bologna,2 Italy
Received 9 April 2001/Accepted 1 June 2001
We have overexpressed and purified the Helicobacter pylori Fur protein and analyzed its interaction with the intergenic regions of divergent genes involved in iron uptake (frpB and ceuE) and oxygen radical detoxification (katA and tsaA). DNase I footprint analysis showed that Fur binds specifically to a high-affinity site overlapping the PfrpB promoter and to low-affinity sites located upstream from promoters within both the frpB-katA and ceuE-tsaA intergenic regions. Construction of an isogenic fur mutant indicated that Fur regulates transcription from the PfrpB promoter in response to iron. In contrast, no effect by either Fur or iron was observed for the other promoters.
Present address: Biophysics Institute, University of Rio de
Janeiro, Rio de Janeiro, Brazil.
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