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. 2005 Aug;187(16):5809–5817. doi: 10.1128/JB.187.16.5809-5817.2005

TABLE 1.

Strains and plasmids used in this study

Strain Description Source or reference
E. coli strains
    BL21 (DE3) FompT hsdSB (rB mB) gal dcm (DE3) (Cmr) Novagen
    JM109 endA1 recA1 gyrA96 thi hsdR17 (rK mK+) relA1 supE44 Δ(lac-proAB) [F′ traD36 proAB laqIqZΔM15] Promega
    ACP1008 JM109 containing pACP1005 This study
    ACP1009 BL21(DE3) containing pACP1005 and pGroESL This study
P. multocida strains
    X-73 Fowl cholera-causing, wild-type strain; serogroup A, serotype 1 42
    ACP13 ΔpnhA::tet(M) (Tetr) This study
    ACP17 ΔpnhA::tet(M) containing pACP1007 This study
Plasmids
    pAL99 P. multocida-E. coli shuttle vector containing promoter region of P. multocida gene tpiA (Knr) B. Adlera
    pET30b Expression vector (Knr) Novagen
    pGroESL Plasmid containing groEL and groES genes and the T7 lac promoter (Cmr) 16
    pVB101 pBR322 containing tet(M) gene from Tn916 (Apr Tetr) 11
    pACP1000 pWSK29 containing entire coding region of pnhA and promoter region (Apr) This study
    pACP1002 pACP1000 containing pnhA::tet(M) mutagenesis cassette (Apr Tetr) This study
    pACP1005 pET30b containing promoterless pnhA gene (Knr) This study
    pACP1007 pAL99 containing pnhA gene from pACP1005 (Knr) This study
a

Kind gift from Ben Adler, Department of Microbiology, Monash University, Victoria, Australia.