Skip to main content
. 2017 Jan 27;6(4):e00451. doi: 10.1002/mbo3.451

Table 1.

Strains and plasmids used in this study

Strain or plasmid Characteristic(s) Source or reference
Strains
A. hydrophila
W1 wild‐type strain
M01 ~ M332 mini‐Tn10Km insertion mutant (SmR KmR) This study
M196 rbsR: mini‐Tn10Km (SmR KmR) This study
MC196 WM196 complemented with pACYC184‐rbsR (CmR) This study
Escherichia coli
SM10 thi thr leu tonA lacY supE recA RP4‐2‐Tc::Mu::Km (λpir)F‐, 80dlacZ ΔM15, Δ(lacZYA‐argF) U169, deoR, recA1 (Herrero et al., 1990)
E. coli DH5α endA1, hsdR17 (rK−, mK+), phoA, supE44, λ‐, thi‐1, gyrA96, relA1
Plasmid
pMD18‐T Cloning vector (ApR) Takara
pLOF/Km Tnl0‐based delivery plasmid with (KmR ApR); (Herrero et al., 1990)
pACYC184 (CmR TcR) provided by Prof. Nie
pACYC184‐rbsR pACYC184 derivative containing 1,005 bp fragment of rbsR putative promoter and ORF(CmR) This study