TABLE 2.
Phenotypic characterization of S. dysenteriae iron transport system mutants
Strain | Genotype or phenotype | Synthesis of enterobactinab | Utilization ofa:
|
||
---|---|---|---|---|---|
Hemin | Enterobactinc | Ferrichrome | |||
SDU378 | Wild type | + | + | + | + |
SDU380 | tonB | + | − | − | − |
SDU380/pYUK1 | TonB+ | + | + | + | + |
SDU400 | shuA | + | − | + | + |
SDU400/pHTL116 | ShuA+ | + | + | + | + |
SDU402 | shuA entB | − | − | + | + |
SDU402/pHTL116 | ShuA+entB | − | + | + | + |
SDU402/pHEB1 | ShuA+ EntB+ | + | + | + | + |
Bioassays were performed as described in Materials and Methods. +, zone of stimulation ≥5 mm. Growth of all strains was stimulated by 20 μl of 10 mM FeSO4.
Enterobactin synthesis was determined by the ability to cross-feed the E. coli entB mutant, AB1515.24.
AB1515 (5 μl of an overnight culture) was used as the enterobactin-producing strain.