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. 1999 Mar;181(6):1853–1860. doi: 10.1128/jb.181.6.1853-1860.1999

TABLE 1.

E. coli strains and plasmids used in this study

Strain or plasmid Description Source or reference
E. coli
 LE392 FhsdR514 (rK mK) lacY1 supE44 supF58 galK2 galT22 trpR55 metB1
 ISM612 [leu(UGA) lacZ659(UGA) trpA9605(UAG) his29(UAG) ilv thyA metB argH rpoB rpsL prfB3] pISM3001 21, 36
 ISM614 LE392 [FhsdR514 (rK mK) lacY1 supE44 supF58 galK2 galT22 trpR55 metB1] pISM3001 This study
 ISM647 XL1-Blue [recA1 lac endA1 gyrA46 thi hsdR17 supE44 relA1 (F′ proAB+ lacIqlacZΔM15 Tn10)] pISM3001 This study
 DPWC F+ mating donor Gold Biotechnologies
 BW26 F mating recipient, Kanr Gold Biotechnologies
 CSR 603 (recA1 uvrA6 phr-1) maxicell strain 33
Plasmids
 pISM3001 trpT gene cloned behind a lac promoter in the vector pACYC184, Cmr 36
 pISM4170 6.6-kb SacI fragment from phage 13-2B cloned onto pMOB, Apr This study
 pISM4172 7.0-kb SacI fragment from phage 13-2B cloned onto pMOB, Apr This study
 pISM4175 2.2-kb ClaI fragment from pISM4172 cloned into pMOB, Apr This study
 pISM4176 2.6-kb ClaI fragment from pISM4172 cloned into pMOB, Apr This study
 pMOB Cloning vector for Tn1000 mutagenesis, Apr Gold Biotechnologies