Complementation of mas::tn in the ΔeccC5 mutant by replacement of the integrated pMV vector.

Indicated strains were electroporated with the input DNA shown on the left. Input DNA consisted of the pMV-361-hyg plasmid containing the indicated constructs. Valid insertion of input DNA was scored as + or-, similarly as described for Table 1. Results are representative data of three independent experiments.

Complementation of mas::tn in the ΔeccC5 mutant by replacement of the integrated pMV vector.