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. 2009 May 1;284(18):11854–11862. doi: 10.1074/jbc.M808583200

TABLE 1.

Strains and plasmids used in this study

Strain or plasmid Description Reference
Strain
    P. aeruginosa
        PAO1 Serotype O5, type strain (27)
    E. coli
        BL21(DE3) General expression strain F-ompT hsdSB(rB-mB-) gal dcm (DE3) Novagen
        Rosetta(DE3) Expression strain with pRARE plasmid (CmR) encoding rare tRNAs Novagen
        Tuner(DE3) Expression strain with lacY deletion for strict regulation of induction by IPTG Novagen
Plasmid
    pLysS Expresses T7 lysozyme to suppress basal expression of T7 RNA polymerase prior to induction Novagen
    pET-28a 5.4-kb T7 expression vector with N- or C-terminal His tags, KmR Novagen
    pET-23dr Derivative of pET-23a T7 expression vector with short linker between N-terminal His tag and protein, AmpR (18)
    pCQW14 PCR from PAO1 template inserted NdeI-XhoI into pET-28a to generate His6-WbpA expression plasmid, KanR (9)
    pET-His6-WbpB PCR from PAO1 template inserted BamHI-EcoRI into pET-28a to generate His6-WbpB expression plasmid, KanR (7)
    pWMJL085 PCR from PAO1 template DNA inserted NcoI-BamHI into pET-23dr vector to generate His6-WbpE expression plasmid, KanR (7)
    pCQW3 PCR from PAO1 template DNA inserted NdeI-HindIII into pET-28a to generate His6-WbpD expression plasmid, KanR (8)
    pWMJL072 pET-23dr-based His6-WbpI expression plasmid, AmpR (11)