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. 2005 Nov;71(11):6808–6815. doi: 10.1128/AEM.71.11.6808-6815.2005

TABLE 1.

Strains, plasmids, and PCR primers used in this study

Strain, plasmid, or primer Description and/or relevant genotypea Reference or source
R. solanacearum strains
    GMI1000 Wild-type strain 29
    R3 GMI1000, spontaneously Rifr This study
    R3-1501 R3::pCN15, Kmr This study
    R3-337 R3::pCN337, Kmr This study
    R3-1530 R3::pCN1530, Kmr This study
E. coli strains
    DH5α Invitrogen
    S17-1 (λpir) Tpr Smr, recA thi hsdRM+, λpir phage lysogen RP4::Mu::Km Tn7 9
Plasmids
    pFSV Cmr Tcrori R6K mob RP4 4
    pFSVIN3 Cmrori R6K mob RP4 ppoA::mini-Tn10 Gmr 21
    pFSVCN ori R6K mob RP4 ′ppoA′ Gmr 21
    pFSVK ori R6K mob RP4 ′ppoA′ Kmr 21
    pBRI15 pBKSII + 180-bp BamHI internal fragment from RSc1501 gene This study
    pCN1501 pFSVK + 235-bp EcoRI-SacI fragment from pBRI15 This study
    pCN337 pFSVK + 300-bp NcoI-SacI fragment from RSc0337 amplified by PCR This study
    pCN1530 pFSVK + 800-bp SacI-EcoRI fragment from RSp1530 amplified by PCR This study
Primers
    F1501 GTTTTCGAATTCTGCCTGACG (EcoRI)
    FI337 TCGCCATGCCGTACTGGAAC (NcoI)
    FI1530 ACGGCGAGCTCGACACCCTG (SacI)
    R1501 GGTGGTGAGCTCCCAATGAAG (SacI)
    RI337 GCGTGAGCTCCAGGATGC (SacI)
    RI1530 ACGGTGAATTCGAACGCGTCG (EcoRI)
a

Engineered restriction sites are underlined.