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. 2002 Jan 29;99(3):1158–1163. doi: 10.1073/pnas.032658999

Table 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Genotype or relevant characteristic Ref. or source
E. coli
 XL1-Blue RecA1, endA1, gyrA96, thi-1, hsdR17, supE44, relA1, lac, [F′, proAB, laclqZΔM15, Tn10 (tetr)] 33, Stratagene
 M15(pREP4) Lac, ara, gal, mtl, recA+, uvr+, [pREP4, lacI, kanr] 34
Plasmids
 pQE30 High copy His-Tag expression vector Qiagen
 pQElytB Expression of ispH (lytB) from E. coli This study
 pACYC184 Low copy cloning vector 35, NEB
 pACYClytB Expression of ispH from E. coli This study
 pACYClytBgcpE Expression of ispG and ispH from E. coli This study
 pBluescript SKII High copy cloning vector Stratagene
 pBScyclo Expression of xylB, ispC, ispD, ispE, and ispF from E. coli 25
 pBSxispC-H Expression of xylB, ispC, ispD, ispE, ispF, ispG, and ispH from E. coli This study