In several Gram-negative pathogens the fur (ferric uptake regulator) g
ene product controls the expression of many genes involved in iron upt
ake and virulence, To facilitate the study of iron-regulated gene expr
ession in Bordetella pertussis, we cloned the fur gene from this organ
ism. The B. pertussis fur gene product was 54% identical to the Escher
ichia coli Fur and complemented two E. coli fur mutants. As with the E
. coli fur gene, sequences upstream of the B. pertussis fur were homol
ogous to the consensus Fur-binding site and to the consensus catabolit
e activator protein binding site.