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. 2012 Apr 26;7(4):e35847. doi: 10.1371/journal.pone.0035847

Table 1. Plasmids used in this study.

Plasmids Description Reference
pFPV27 E. coli-Mycobacterium shuttle plasmid with promoterless gfp, kmr [52]
pDSDevR devR coding sequence and 327 bp upstream region cloned in pFPV27 (low copy number plasmid), hygr [12]
pOperon Rv3134c-devRS operon promoter (−608 to +998) cloned in pFPV27, hygr [16]
p3134c-1 Rv3134c promoter (−608 to +90) cloned in pFPV27, hygr [16]
pJFR19 3-kb amidase promoter cloned in mycobacterial integrative vector pMV306H, hygr [53]
pMG85 devR coding region cloned downstream of amidase promoter in integrative vector pJFR19, hygr [54]
pSM POperon devR Rv3134c-devRS operon promoter (−608 to +998) replaces amidase promoter in pMG85, hygr This study
pSM PRv3134c devR Rv3134c promoter (−608 to +90) replaces amidase promoter in pMG85, hygr This study
pSM PdevR devR devR promoter (−327 to −1) replaces amidase promoter in pMG85, hygr This study
pKKNKan pET-28a- based plasmid for overexpression of DevRN-Kan fusion protein, Kanr [15]
pAVDevR pET-28a- based plasmid for overexpression of intact DevR protein, Kanr [15]