Table 3.
Strain, plasmid, or oligonucleotide | Relevant characteristics1 or sequences (5′ 3′) | Reference |
---|---|---|
Pseudomonas protegens | ||
CHA0 | Wild type; biocontrol agent; DAPG+, PRN+, HCN+ | Stutz et al., 1986 |
CHA0-gfp | CHA0::attTn7-gfp; Gmr | Péchy-Tarr et al., 2013 |
Pseudomonas chlororaphis | ||
PCL1391 | Wild type; biocontrol agent; HCN+, PHZ+ | Chin-A-Woeng et al., 1998 |
PCL1391-gfp | PCL1391::attTn7-gfp; Gmr | This study |
Escherichia coli | ||
DH5α | Laboratory strain | Sambrook and Russell, 2001 |
Plasmids | ||
pBK-miniTn7-gfp2 | pUC19-based delivery plasmid for miniTn7-gfp2; mob+ Gmr Cmr Aprr | Koch et al., 2001 |
pME7116 | prnA-gfp transcriptional fusion; reporter of PRN biosynthetic gene expression in CHA0;Tcr | Baehler et al., 2005 |
pME9010 | mCherry-based promoter-probe vector derived from pPROBE’-gfp (AAV); Kmr | Rochat et al., 2010 |
pME9011 | hcnA-mcherry transcriptional fusion; reporter of HCN biosynthetic gene expression in CHA0; Kmr | Rochat et al. (2010) |
pME9012 | phlA-mcherry transcriptional fusion; reporter of DAPG biosynthetic gene expression in CHA0; Kmr | Rochat et al., 2010 |
pME11011 | prnA-mcherry transcriptional fusion; reporter of PRN biosynthetic gene expression in CHA0; Kmr | This study |
pME11017 | phzA-mcherry transcriptional fusion; reporter of PHZ biosynthetic gene expression in PCL1391; Kmr | This study |
pUK21 | Cloning vector; Kmr | Vieira and Messing, 1991 |
pUX-BF13 | Helper plasmid encoding Tn7 transposition functions; R6K-replicon; Apr | Bao et al., 1991 |
Oligonucleotides2 | ||
P5 BamHI new | CGGGATCCCGGGCTCAAGGACAGTTGGTTCA, BamHI | This study |
P6 | GGAATTCCCGAGGTACGAAGCGGCCATC, EcoRI | Baehler et al., 2005 |
phzAF | CGGGATCCCTAACTCCATTTTGAGCACC, BamHI | This study |
phzAR | CGAGCTCGCTCAATCTCCAATGAATAAGGGGGCT, SacI | This study |
1Abbreviations: Apr, ampicillin; Cmr, chloramphenicol; Gmr, gentamicin; Kmr, kanamycin; and Tcr, tetracycline resistance, respectively.
2Restriction sites are underlined.