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. 2017 Dec 21;12(12):e0188179. doi: 10.1371/journal.pone.0188179

Table 1. Strains and plasmids used in this study.

Strain or plasmid Description Source or reference
Bacterial strains
Escherichia coli DH5α F- Φ80dlacZΔM15 recA1 endA1 gyrA96 thi-1 hsdR17 (rk- mk+) supE44 relA1deoRΔ(lacZYA-argF) U169 Promega, Madison, WI
Escherichia coli HB101 F- hsdS20 (rB- mB-) recA13 ara-14 proA2 lacY1 galK2rpsL20 (Strr) xyl-5 mtl-1 supE44 thi-1 leuB6 Promega, Madison, WI
Bacillus subtilis 168 trpC2 [26]
Bacillus subtilis subsp. krictiensis ATCC55079 Wild-type [28]
Fungi
Fusarium oxysporum Wild-type This study
Magnaporthe grisea Wild-type This study
Trichophyton mentagrophytes Wild-type This study
Plasmids
 pTZ18R Ampr plasmid carrying the T7 g10 promoter [31]
 pLAFR1 pRK290 containing the cos site [32]
 pLAFR3 pLAFR1 containing an HaeII fragment of pUC8 [32]
 pIC333 Mini-Tn10 delivery vector [33]
 pJJ5, pJJ71, pJJ121, pJJ815 Genomic library clones constructed using cosmid vector pLAFR3 This study
 pJJ121E2 16.4-kb EcoRI-digested pJJ121 fragment inserted into pTZ18R This study
 pJJ121E3 4.8-kb EcoRI-digested pJJ121 fragment inserted into pTZ18R This study
 pJJ815E4 3.7-kb EcoRI-digested pJJ815 fragment This study
 pJJ121E2-2 7.9-kb EcoRI and SalI-digested pJJ121E2 fragment inserted into pBC KS(+) This study
 pJJ121E2-1 BamHI and XbaI-digested pIC333 fragment inserted into the ClaI site of pJJ121E2-2 This study