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. 2021 Aug 31;12(4):e00656-21. doi: 10.1128/mBio.00656-21

FIG 3.

FIG 3

Activity of Fpn homologs from BfN and susceptible target strains. (A) Western blot analysis of BFT products generated following incubation of purified BfN Fpn or its catalytic residue mutants (FpnH135A; FpnC180A) with BFT carrying a C-terminal c-Myc tag. (B) Mutation of Fpn catalytic residues in BfN abrogates its ability to inhibit BfR growth. The mean number of target strain input CFU is indicated with a gray line (mean = 6.0 × 107); line width represents SD (SD = 5.0 × 106). Target strain output CFU are reported. Error bars indicate SD (n = 2; representative of three independent experiments). (C) Expression of fpn genes derived from susceptible strains BfH610 and BfH615 restores killing activity to a BfNΔfpn mutant. The mean number of target strain input CFU is indicated with a gray line (mean = 9.6 × 105); line width represents SD (SD = 2.4 × 105). Target strain output CFU are reported. Error bars indicate SD (n = 2; representative of three independent experiments). For panels B and C, different letters represent groups that are statistically significantly different (P < 0.05).