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. 2011 Sep;193(18):4849–4858. doi: 10.1128/JB.05051-11

Table 2.

Strains used in this study

M. tuberculosis straina Relevant features Reference or source
ΔdevR mutant 447-bp BalI deletion in M. tuberculosis H37Rv devR gene (deletes DevR amino acid residues from position 40 to 191) 27
Comp13* ΔdevR mutant complemented with pSD POperondevR; expresses WT DevR protein 22
Comp17* ΔdevR mutant complemented with pUS POperondevR T82A; expresses DevR T82A mutant protein This study
Comp18 Comp17 electroporated with p1738 (GFP reporter plasmid) This study
a

*, M. tuberculosis strains of similar genetic backgrounds that produce DevR T82A (Comp17) or WT protein (Comp13) from a single copy of devR integrated at identical chromosomal locations.