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. 2017 Sep 11;18:715. doi: 10.1186/s12864-017-4127-2

Table 3.

Main bacterial strains and plasmids used in this study

Bacterial strain or plasmid Relevant characteristicsa Source or reference
Escherichia coli
 DH5α Cloning host; F λ endA1 glnX44(AS) hiE1 recA1 relA1 spoT1 gyrA96(NalR) rfbC1 deoR nupG Φ80(lacZΔM15) Δ(argF-lac)U169 hsdR17(r K m K +) TransGen Biotech, Beijing, China
 S17–1 (λpir) Donor strain; res pro mod + integrated copy of RP4, mob+, used for incorporating constructs into P. chlororaphis Lab stock; Hoffmann et al.
Pseudomonas chlororaphis
 GP72 P. chlororaphis GP72 wild-type strain Lab stock; Liu et al.
 GP72(rpeA-) GmR, rpeA insertionally inactivation mutant of GP72 Lab stock; Huang et al.
 MDS5 GmR, mutant of GP72(rpeA-) with deletion of 1.40% of the genome, including five secondary metabolic gene clusters This study
 MDS10 GmR, mutant of GP72(rpeA-) with deletion of 3.52% of the genome This study
 MDS22 GmR, mutant of GP72(rpeA-) with deletion of 10.29% of the genome This study
Plasmid
 pK18 mobsacB Broad-host-range gene replacement vector,
sacB, KmR
Lab stock; Schafer et al.
 pK18- MDXb pK18 mobsacB containing MDX flanking
region
This study

aAntibiotic markers: Km, kanamycin

bMDX means the corresponding multiple-deletion region