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Table 3 Main bacterial strains and plasmids used in this study

From: Developing genome-reduced Pseudomonas chlororaphis strains for the production of secondary metabolites

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

  1. aAntibiotic markers: Km, kanamycin
  2. bMDX means the corresponding multiple-deletion region