Iron regulation in a growing number of bacterial species is being attr
ibuted to the presence of a fur (ferric uptake regulation) regulatory
system. In the presence of iron, Fur acts as a classical negative regu
lator, binding conserved sequences within the promoter of iron-repress
ible genes and blocking transcription. Western blot analysis utilizing
Escherichia coli Fur antisera detected a band of approximately 17 kDa
in soluble extracts of Haemophilus ducreyi. Additionally, Southern bl
ot hybridization of the H. ducreyi chromosome with a meningococcal fur
probe indicated that H. ducreyi might contain a fur homolog. This put
ative fur homolog was cloned into the E. coli vector pACYC184. This cl
one was capable of repressing expression of a normally Fur-regulated l
acZ fusion in the fur-background of E. coli strain H1780. The deduced
amino acid sequence shows H ducreyi fur to be 54% identical and 73% si
milar to E. coli fur, containing putative DNA-binding and metal-bindin
g domains. These data demonstrate that H ducreyi has a functional fur
system.