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. 1999 Feb;181(3):726–730. doi: 10.1128/jb.181.3.726-730.1999

TABLE 1.

Bacterial strain and plasmids used in this study

Strain or plasmid Relevant characteristic(s) Source or reference
Strain
E. coli XL1-Blue recA1 endA1 gyrA96 thi hsdR17 supE44 relA1 lac/[F′::Tn10 proAB+ lacIqlacZM15 traD36] 2
Plasmids
 pBluescriptII SK+ Apr ColE1 replicon, cloning vector Stratagene
 pSTV29 Cmr pACYC replicon, cloning vector 4, 25
 pTUE1122 Aprtac promoter, 6xHis, expression vector 16
 pMR26 Broad-spectrum mercury resistance plasmid from Pseudomonas strain K-62 8, 10
 pMRA17 6.6-kb SacI fragment of pMR26 containing merRTPAGB cloned into pBluescriptII SK+ 8, 10
 pMR96 4.7-kb BglII-EcoRV fragment of pMRA17 containing merRTPAGB cloned into pBluescriptII SK+ This study
 pMC89 merB-deleted plasmid, containing merRTPAG, constructed from pMR96 This study
 pMU29 merG-deleted plasmid containing merRTPAB cloned into pBluescriptII SK+ 10
 pMRD141 merAGB-deleted plasmid containing merRTP, constructed from pMRA17 9, 10, 31
 pMEV89 1.2-kb HindIII-BamHI fragment of pMC89 containing merG cloned into pSTV29 This study
 pMUE74 697-bp PCR products of merG cloned into pTUE1122 This study