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. 2009 Jan 2;284(1):56–66. doi: 10.1074/jbc.M806068200

TABLE 1.

Strains and plasmids used in this study

Strain or plasmid Description of strain or plasmid Source
E. coli
    S17.1 E. coli shuttle vector. 294(recA, pro res mod+) Tpr, Smr, (pRP4-2 Tc::Mu-Km::Tn7) (61)
P. aeruginosa
    MPAO1 Wild-type P. aeruginosa PAO1 Pseudomonas Genome Center, Seattle, WA
    7520 phuS mutant containing ISlacZ/hah transposon insertion, derived from MAPO1 (as above)
    CDC-5 pvd-2 derivative of PAO1 strain lacking pyoverdin production (35)
    IA614 Pyochelin-deficient derivative of CDC-5 strain, obtained by ethylmethanesulfonate mutagenesis (35)
    IR1648 Chromosomal knockout of iron-regulated heme oxygenase gene, hemO derived from IA614 (46)
    IA614-ΔphuS Chromosomal knockout of phuS derived from IA614 This study
    IR1648-ΔphuS Chromosomal knockout of phuS derived from IR1648. This mutant lacks both pigA and phuS along with the siderophores pyochelin and pyoverdin This study
Plasmids
    pEX18p AmpR; allelic replacement vector (34)
    pFlp2 AmpR; source of Flp recombinase (34)
    pPS856 Source of GentR-GFP, GentR-conferring fragment flanked by FRT sites (34)
    pFTC1 Source of TetR-GFP, TetR-conferring fragment flanked by FRT sites H. Schweizer
    pEX18p-ΔphuS::Gm AmpR; allelic replacement vector containing 1.8-kb fragment of in-frame phuS deletion containing the GentR antibiotic marker This study
    pEX18p-ΔphuS::tet AmpR; allelic replacement vector containing 1.8-kb fragment of in-frame phuS deletion containing the TetR antibiotic marker This study