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. 2013 Jun;195(12):2852–2863. doi: 10.1128/JB.00244-13

Table 1.

Strains and plasmids used in this study

Strain or plasmid Relevant characteristics or use Reference or source
C. diphtheriae strains
    1737 Wild type, Gravis biotype, Tox+ 37
    1737htaAΔ htaA deletion mutant of 1737 25
    1737htaBΔ htaB deletion mutant of 1737 25
    1737chtAΔ chtA deletion mutant of 1737 This study
    1737chtBΔ chtB deletion mutant of 1737 This study
    1737chtCΔ chtC deletion mutant of 1737 This study
    1737chtAΔ/chtBΔ Deletion of chtA and chtB in 1737 This study
    1737htaBΔ/chtBΔ Deletion of htaB and chtB in 1737 This study
    1737chtAΔ/chtCΔ/htaAΔ Deletion of chtA, chtC, and htaA in 1737 This study
    1737chtAΔ/chtCΔ Deletion of chtA and chtC in 1737 This study
    C7(−) Wild type, Tox 38
    C7dtxRΔ C7 dtxR deletion mutant 25
E. coli strains
    BL21(DE3) Protein expression Novagen
    DH5α Cloning strain Invitrogen
    S17-1 RP4 mobilization functions 32
    TOP10 Cloning of PCR fragments Invitrogen
    XL1-Gold Mutagenesis strain Stratagene
Plasmids
    pCR-Blunt-IITOPO Cloning of PCR fragments, Knr Invitrogen
    pSPZ Promoter probe, Spcr 28
    pGEX-6P-1 Expression vector (GST fusion), Ampr GE Healthcare
    pET24(a)+ Expression vector, Knr Millipore
    pKN2.6Z C. diphtheriae shuttle vector, Knr 24
    pKhtaA pKN2.6Z carrying the htaA gene 25