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. 2018 Aug 7;9:1789. doi: 10.3389/fmicb.2018.01789

Table 1.

Bacterial strains and plasmids used in this study.

Strain or plasmid Genotype or description Reference
Plasmids
   pK18mob Suicide vector to create a mutant by a single crossover; Kanr Schäfer et al., 1994
   pK18mobsacB Suicide vector to create mutant by double crossover recombination; Kanr Schäfer et al., 1994
   pLAFRJ Shuttle plasmid pLAFR3 derivate containing the multiple cloning sites of pUC19; Tcr Jiang et al., 2009
Strain
   Xoc GX01 Wild-type strain; Rifr Lab collection
   E. coli DH5α Used for molecular cloning Lab collection
   NK0263–NK4109 (a total of 50 strains) GX_XOC0263 to GX_XOC4109 (a total of 50 genes), mutants with insertions of response regulator genes of Xoc GX01, constructed by pK18mob vector integration; Kanr This study
   CNK2201 Genetic complementary strain of NK2201 (mutant of GX_XOC2201); Rifr, Kanr, Tcr This study