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. 2006 Oct 6;188(24):8376–8384. doi: 10.1128/JB.00763-06

TABLE 1.

Bacterial strains and plasmids used in this study

Bacterial strain or plasmid Relevant characteristicsa Reference or source
Escherichia coli
    DH5a F λ φ80dlacZΔM15 Δ(lacZYA-argF)U169 recA1 endA1 hsdR17(rK mK+) supE44 thi-1 gyrA relA1 Takara, Kyoto, Japan
    S17-1 thi pro hsdR hsdM+recA [chr::RP4-2-Tc::Mu-Km::Tn7] 26
Chromobacterium violaceum CV026 Double mini-Tn5 mutant from C. violaceum ATCC 31532; AHL biosenser 22
Pseudomonas syringae pv. tabaci
    6605 Wild type; Nalr 30
    6605-d3 6605 Δorf3 33
    6605-dpsyI 6605 ΔpsyI This study
Plasmids
    pGEM-T Easy 3.015-kb cloning vector for PCR product; Ampr Promega, Tokyo, Japan
    pK18mobsacB Small mobilizable vector; Kmr; sucrose sensitive (sacB) 26
    pDSK519 Broad-host-range cloning vector; Kmr 16
    pM3 1.69-kb chimeric PCR product deleting orf3 cloned into pK18mobsacB at EcoRI site; Kmr 33
    pDSKGI 9-kb HindIII fragment containing orf1, orf2, and orf3 genes from P. syringae pv. tabaci 6605 in pDSK519; Kmr 33
a

Ampr, ampicillin resistance; Kmr, = kanamycin resistance; Nalr, nalidixic acid resistance.