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. 2008 Sep 26;190(23):7621–7632. doi: 10.1128/JB.00806-08

TABLE 1.

Bacterial strains, bacteriophage, and plasmids used in this study

Bacterial strain, bacteriophage, or plasmid Relevant propertiesa Source or reference
Bacterial strains
    DH5α E. coli cloning host Invitrogen
    RN4220 S. aureus restriction-deficient strain 8325-4 49
    1457 S. epidermidis biofilm-forming strain 43
    1457-acnA Strain 1457 acnA inactivated mutant; Minr This study
    1457-citZC Strain 1457 citCZ deletion mutant; Ermr This study
    1457-Δica Strain 1457 icaADBC deletion mutant; Tmpr 26
    1457-icaR Strain 1457 icaR inactivated mutant; Minr 26
    1457-sigB Strain 1457 sigB inactivated mutant; Tmpr 26
    1457-sarA Strain 1457 sarA inactivated mutant; Minr 26
Bacteriophage 71 S. epidermidis transducing phage 15
Plasmids
    pCL15 Expression vector; derivative of pSI-1; Camr Chia Lee
    pEC4 pBluescript II KS(+) with ermB inserted into ClaI site; Ampr Ermr 5
    pJF12 Plasmid pCR2.1 containing tetM; Ampr Minr J. Finan and G. Archer
    pGEM-T E. coli TA cloning vector; Ampr Promega
    pMRS2 pCL15 with acnA gene under the control of the Pspac promoter; Camr This study
    pMRS5 Derivative of pTS1-d with citZC::ermB fragment; Ampr Camr Ermr This study
    pNF103 pUC19 with 1.7-kb internal fragment of acnA; Ampr This study
    pNF117 pNF103 with tetM inserted into EcoRI site; Ampr Minr This study
    pNF118 pRO6448::pNF117; Ampr Ermr Minr This study
    pRO6448 pE194(ts) with AluI fragment (oriT) of pC221 cloned into the unique ClaI site; Ermr 51
    pTS1 Shuttle vector; pE194orits; ColE1; Ampr Camr 24
    pTS1-d Derivative of pTS1 with deletion of plasmid-encoded 3′ region of ermC This study
    pUC19 E. coli cloning vector; Ampr 83
a

Ampr, ampicillin resistant; Camr, chloramphenicol resistant; Ermr, erythromycin resistant; Minr, minocycline resistant; Tmpr, trimethoprim resistant; ts, temperature-sensitive origin of replication.