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. 2004 Mar;70(3):1836–1842. doi: 10.1128/AEM.70.3.1836-1842.2004

TABLE 1.

P. fluorescens strains and plasmids used in this study

Strain or plasmid Genotype and relevant characteristicsa Reference
Strains
    CHA0 Wild type from Morens, Switzerland; DAPG+ HCN+ 63
    CHA5 hcnB::Ω-Hg insertion derivative of CHA0; Hgr DAPG+ HCN 64
    CHA207 Chromosomal hcnA′-′lacZ fusion of CHA0; DAPG+ HCN 7
    CHA630 phlH::Tn5 single-chromosomal-insertion derivative of CHA0; Kmr DAPG HCN+ 52
    CHA631 ΔphlA in-frame-chromosomal-deletion derivative of CHA0; DAPG HCN+ 52
    Q2-87 Wild type from Washington State; DAPG+ HCN 62
    Q2-87::Tn5-1 phlD::Tn5-1 chromosomal-insertion derivative of Q2-87; Kmr DAPG HCN 3
Plasmids
    pME3013 pVK100 with an 8-kb genomic fragment of CHA0 containing functional hcnABC genes conferring HCN biosynthesis; Tcr 64
    pME6259 pACYC177-pVS1 carrying a lacZ translational fusion to the phlA of CHA0; Tcr 52
    pME6261 pACYC177-pVS1 with a 2-kb fragment of CHA0 containing a functional phlA of CHA0 conferring DAPG biosynthesis; Tcr 52
    pMON5118 pCP13/B with a 35-kb genomic fragment of Q2-87 containing the DAPG biosynthetic locus conferring DAPG biosynthesis; Tcr 62
a

+, positive for production; −, no production; Hgr, mecury resistant (20 μg ml−1); Kmr, kanamycin resistant (25 μg ml−1); Tcr, tetracycline resistant (125 μg ml−1 for P. fluorescens).