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. 2016 Mar 17;198(7):1114–1122. doi: 10.1128/JB.00954-15

TABLE 2.

Plasmids used in this study

Plasmid Relevant characteristic(s)a Reference or source
pAJ22 β-Galactosidase reporter plasmid; Cmr 25
pCL52.2 Temp-sensitive shuttle vector; Tcr Spr 19
pCM12 E. coli/S. aureus shuttle vector with PsarA-sodARBS-gfp (superfolder); Ampr Spr 24
pCN51 Pcad-inducible plasmid; Ampr Ermr 22
pET24b IPTG-inducible E. coli expression plasmid Novagen
pET24b-srrA pET24b with gene encoding SrrA This study
pIHW5 Pcad-inducible lacZ reporter plasmid; Ampr Ermr This study
pIHW7 Promoterless lacZ reporter plasmid; Ampr Ermr This study
pIHW10lac cidABC reporter plasmid; Ampr Ermr This study
pIHW58 srrAB complementation plasmid; Tcr Spr This study
pJB12 Temp-sensitive UAMS-1 ΔcidB plasmid (pCL52.2) This study
pJB60 Temp-sensitive allelic-exchange plasmid with counterselection; Ampr Cmr This study
pJB60-114115 Temp-sensitive UAMS-1 ΔcidABC plasmid; Ampr Cmr This study
pJB61 Temp-sensitive allelic-exchange plasmid with counterselection; Ampr Cmr This study
pJB67 pCN51 with TIR; Ampr Ermr This study
pJB94 E. coli/S. aureus shuttle vector; Tcr Spr This study
pJB97 UAMS-1 cidB complement plasmid; Ampr Ermr This study
pRN8298 pI258 replicon; Ampr Ermr 22
a

TIR, optimized transcription initiation region.