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. 2014 Nov 27;2014:428159. doi: 10.1155/2014/428159

Table 2.

Strains and plasmid used in this study.

Construct/strain Characteristic Source
E. coli DH5α supE44ΔlacU169 hsdR17 recA1 endA1 gyrA96 thi-1 relA1Φ80 dlacZ ΔM15 Invitrogen
E. coli BL21 (DE3) pLysS F-ompT hsdSB(rBmB−) gal dcm(DE3)plysS(CmR) Novagen
E. coli TOP10 F-Φ80lacZΔM15 Δ(lacZYA-argF) U169 recA1 endA1 hsdR17 (rK–, mK+) phoA supE44 λ-thi-1 gyrA96 relA1 Invitrogen
E. coli BL21 (DE3) F-ompT hsdSB(rB–, mB–) gal dcm (DE3) Novagen
pET 28 (a) 5.3 kb expression vector; kanr Novagen
pBAD His (c) 4.1 kb, L-arabinose regulated pBR322-derived expression vectors designed for regulated, recombinant protein expression and purification in E. coli. Invitrogen
pGEX4T1 4.96 kb, bacterial vector for expressing fusion proteins with a thrombin site, GST tagged GE Healthcare
pJSL/JSL pBAD His (c) alone without insert in E. coli Top 10 cells Present study
pJSL1/JSL1 pGEX4T vector containing 285 bp RelB toxin gene from RelE TA module of X. nematophila. Present study
pJSL2/JSL2 pET 28 (a) vector containing 252 bp RelE antitoxin gene from RelE TA module of X. nematophila. Present study
pJSL3/JSL3 pBAD vector containing 285 bp RelE toxin gene from RelE TA module of X. nematophila. Present study
pJSL4/JSL4 pBAD vector containing 526 bp full RelE operon from the genome of X. nematophila. Present study