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. 2020 Feb 11;295(12):3851–3864. doi: 10.1074/jbc.RA119.011692

Table 1.

Strains and plasmids used in this study

Bacterial strains and plasmids Genotype or description Reference/source
E. coli strains
    DH5αλpir fhuA2 lac(del)U169 phoA glnV44 Φ80lacZ(del)M15 gyrA96 recA1 relA1 endA1 thi-1 hsdR17 λpir
    SM10λpir thi thr leu tonA lacY supE recA::RP4-2-Tc::Mu Kmr λpir
P. aeruginosa strains
    PAO1 WT, laboratory strain of P. aeruginosa This study
    PAO1ΔdksA1 WT with dksA1 deletion This study
    PAO1ΔdksA2 WT with dksA2 deletion This study
    PAO1ΔdksA1dksA2 WT with dksA1 and dksA2 double deletion This study
    ΔlasRrhlR WT with lasR and rhlR double deletion
Other strain
    C. violaceum CV026 Biosensor for C4-HSL
Plasmids
    pCVD442 Ampr suicide vector containing sacB for screening recombinant Ref. 10
    pKDT17 Ampr pTS400 plasmid containing lasR and lasB transcriptionally fused with lacZ Ref. 61
    pCVD442d1 pCVD442-containing overlapped left- and right-flanking region of dksA1 This study
    pCVD442d2 pCVD442-containing overlapped left- and right-flanking region of dksA2 This study
    puc18-mini-Tn7t-Gm-lacZ Ampr, Gmr, site-specific chromosomal insertion plasmid harboring promoterless lacZ Ref. 57
    pTNS2 Helper plasmid containing site-specific recombinase for chromosomal insertion Ref. 57
    pD1Tn7t-comp Complementation plasmid contacting dksA1 fragment in puc18-mini-Tn7t-Gm-lacZ This study