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. 2017 Dec 1;7(1):e00520. doi: 10.1002/mbo3.520

Table 1.

General characterization of MxiI mutants

Strains Colony color Noninductible secretion CR induction % Hemolysis % Invasion
Translocators Effectors
M90T Red + + + 100 ± 0.97 100 ± 3.2
mxiI White 0.73 ± 0.56 0 ± 1.2
mxiI + Red + + + 99.25 ± 1.72 104 ± 7.3
mxiC Hyper‐red +++ Delayed + 1.17 ± 0.84 9 ± 1.7
mxiID17A Red + + + 98.5 ± 2.87 95 ± 4.6
mxiIL26A White Reduced Reduced 7.67 ± 1.84 2 ± 1.9
mxiIP55A Red + + + 135.77 ± 1.22 97 ± 4.6
mxiIP60A Red + + + 103.86 ± 5.08 92 ± 6.4
mxiIL63A White 0.79 ± 0.64 2 ± 2.6
mxiIQ67A a Pink +a +a a 55.41 ± 8.3 76 ± 5.2
mxiIQ67E Pink + + 65.43 ± 8.9 39 ± 2.9
mxiIQ67K Red + + + 67.16 ± 0.65 41 ± 3.7
mxiIL70A Red + + + 105.24 ± 7.19 96 ± 1.8
mxiIY73A Red + + + 101.42 ± 2.34 65 ± 7.2
mxiIS71A Red + + + 90.34 ± 10.58 101 ± 2.1
mxiIT82R Hyper‐red +++ Delayed + 1.85 ± 1.46 35 ± 3.2
mxiIT82K Hyper‐red +++ Delayed + 3.40 ± 1.69 52 ± 8.4
mxiIT82A Red + + + 87.32 ± 8.99 92 ± 6.2
mxiIT82E Red + + + 71.98 ± 9.95 95 ± 5.3

In blank: residues mutated by site‐directed mutagenesis based on the homology between MxiI and MxiH. In grey: residues mutated by random mutagenesis on mxiI and harboring a mxiC‐like phenotype.

CR, Congo red.

a

Cherradi et al. (2013).