Table 2.
V. vulnificus strain or genotype | Growth on indicated iron sourcea |
||
---|---|---|---|
FAC | Vulnibactin | Hydroxamate | |
WT | + | + | + |
ΔtonB1 | + | + | + |
ΔtonB2 | + | + | + |
ΔttpC2 | + | + | + |
ΔtonB3 | + | + | + |
ΔtonB1 ΔtonB2 | + | − | − |
ΔtonB1 ΔttpC2 | + | − | − |
ΔtonB1 ΔtonB3 | + | + | + |
ΔtonB2 ΔtonB3 | + | + | + |
ΔtonB1 ΔtonB2 ΔtonB3 | + | − | − |
ΔtonB1 ΔttpC2 ΔttpC3/pMMB208 | + | − | − |
ΔtonB1 ΔttpC2 ΔttpC3/pttpC2(Vvul) | + | + | + |
Growth was determined by the presence of a halo (+) or lack thereof (−) around the iron source indicated. FAC, which does not require active transport, was added as a positive control to confirm that the strain imbedded within the plate was viable. Two microliters of FAC was spotted (500 μg/ml). Wild-type V. vulnificus was streaked onto the plate, and the halo of growth was monitored around the streak. A V. vulnificus ΔvenB mutant strain that is deficient in the production of vulnibactin was streaked onto the plate, and the halo of growth was monitored around the streak.