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. 2009 Jul 31;191(19):6075–6081. doi: 10.1128/JB.00310-09

TABLE 1.

Plasmids used in this study

Plasmid Relevant featuresa Reference
pFPV27 E. coli-mycobacterial shuttle plasmid with promoterless gfp; Kmr 28
pTGS pFPV27 containing tgs1 promoter (−143 to +45); Hygr This study
p3131 pFPV27 containing Rv3131 promoter (−150 to +38); Hygr This study
pTGS-P mut pTGS containing mutated P DevR binding site; Hygr This study
pTGS-S mut pTGS containing mutated S DevR binding site; Hygr This study
pTGS-PS mut pTGS containing mutated P and S DevR binding site; Hygr This study
p3131-P mut p3131 containing mutated P DevR binding sites; Hygr This study
p3131-S mut p3131 containing mutated S DevR binding site; Hygr This study
p3131-PS mut p3131 containing mutated P and S DevR binding site; Hygr This study
pTGS P-inv pTGS containing inverted P DevR binding site; Hygr This study
p3131 P-inv p3131 containing inverted P DevR binding site; Hygr This study
pTGS-ΔS pTGS with S DevR binding site deletion; Hygr This study
p3131-ΔS p3131 with S DevR binding site deletion; Hygr This study
a

Promoter coordinates are with reference to the TSP.