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. 2014 Nov;196(22):3881–3889. doi: 10.1128/JB.01978-14

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Relevant characteristicsa Source or reference
Strains
    E. coli
        JM109 E. coli strain for transformation TaKaRa
        DH5α E. coli strain for transformation TaKaRa
        S17-1 Mobilizer strain 14
    P. aeruginosa
        PAO1 Wild type 36
        ΔccoN1 mutant PAO1 with a markerless deletion of ccoN1 gene This study
        ΔccoN2 mutant PAO1 with a markerless deletion of ccoN2 gene This study
        ΔccoN1 ΔccoN2 mutant PAO1 with markerless deletions of ccoN1 and ccoN2 genes This study
        Δnir mutant PAO1 with markerless deletions of nirS to nirN genes 15
        ΔccoN1 ΔccoN2 Δnir mutant PAO1 with markerless deletions of ccoN1, ccoN2, and nirS to nirN genes This study
        PS1700 narG; 3,835 bp deleted from PA3874 to PA3876 12
Plasmids
    pHSG398 Cloning vector; Cpr TaKaRa
    pG19II pK19mobsac derived suicide vector; sacB Gmr 13
    pG19ccoN1 ccoN1 deletion cassette in pG19II This study
    pG19ccoN2 ccoN2 deletion cassette in pG19II This study
    pG19nir nirS-to-nirN deletion cassette in pG19II 15
    pMEX9 pME4510 derived promoter-probe vector; xylE Gmr 8
    pMEXccoN1 ccoN1 promoter region in pMEX9 This study
    pMEXccoN2 ccoN2 promoter region in pMEX9 This study
a

Cpr, chloramphenicol resistant; Gmr, gentamicin resistant.