Mutagenesis of Vibrio cholerae with TnphoA, followed by screening for fusio
ns that were activated under low-iron conditions, led to the identification
of seven independent fusion strains, each of which was deficient in the ab
ility to utilize ferrichrome as a sole iron source for growth in a plate bi
oassay and had an insertion in genes encoding products homologous to Escher
ichia coli FhuA or FhuD. Expression of the gene fusions was independent of
IrgB but regulated by Fur. We report here a map of the operon and the predi
cted amino acid sequence of FhuA, based on the nucleotide sequence. Unlike
those of the E. coli fhu operon, the V. cholerac ferrichrome utilization ge
nes are located adjacent and opposite in orientation to a gene encoding an
ATP-binding cassette transporter homolog, but this gene, if disrupted, does
not affect the utilization of ferrichrome in vitro.