Skip to main content
. 2002 Dec;68(12):6353–6360. doi: 10.1128/AEM.68.12.6353-6360.2002

TABLE 1.

Bacterial strains and plasmids used in this work

Strain or plasmid Relevant characteristicsa Source or reference(s)
Strains
    A. baumannii
        9235, 8971, 8143, 8114, 8637, 7133, 7138, 8399, 9606, 7931, 9124, 9397 Clinical isolates representing plasmid profiles A to K and W, respectively 2, 22
        BM4420, BM4421, BM4422, BM4424, BM4427, BM4430, BM4432, BM4436, BM4439 Clinical isolates representing RAPD types A to F, H, I, and K, respectively 46
    E. coli
        DH5α Used for recombinant DNA methods Gibco-BRL (Gaithersburg, Md.)
        TransforMax EC100D pir+, used to clone R6K derivatives Epicentre (Madison, Wis.)
        CC118, SM10, and S17-1 λpir, used to maintain and conjugate suicide plasmid pLOFKm 10, 26
Plasmids
    pLOFKm Suicide plasmid harboring mini-Tn10Km; Ampr Kmr 26
    pVK100 Cosmid cloning vector; Kmr Tetr 33
    pRK2073 Conjugation helper plasmid 37
    pWH1266 E. coli-Acinetobacter shuttle plasmid; Ampr Tetr 28
    pFVP25 ColEI, mob+, Ampr; source of the BamHI-PstI fragment harboring gfp 56
    pBCSK+ Cloning vector; Cmr Stratagene (La Jolla, Calif.)
    pMU125 pWH1266 with gfp under control of the Tet promoter This work
a

Ampr, ampicillin resistant; Kmr, kanamycin resistant; Tetr, tetracycline resistant; RAPD, random amplified polymorphic DNA.