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. 1999 Aug;181(15):4704–4707. doi: 10.1128/jb.181.15.4704-4707.1999

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Relevant characteristics Source or reference
E. coli strains
 DH5α supE44 ΔlacU169 (φ80 lacZΔM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1 14
 JM109 recA1 supE44 endA1 hsdR17 gyrA96 relA1 thiΔ(lac-proAB) F′ (traD36 proAB+ lacIqlacZΔM15) 25
Plasmids
 pSC300 luxR in pKK223-3, Apr 4
 pSC156 luxR with deletion of sequences encoding N-terminal amino acids 2–156 of LuxR in pKK223-3, Apr 3
 pSUP102 pACYC184, RP4, Cmr Tcr Mob+ 19
 pAMS121 1-kb BamHI fragment with ptac-luxR from pSC300 in BamHI site of pSUP102, Cmr Tcs Mob+ This study
 pAMS122 0.6-kb BamHI fragment with ptac-ΔluxR from pSC156 in BamHI site of pSUP102, Cmr Tcs Mob+ This study
 pJE202 9-kb SalI fragment of V. fischeri DNA (luxR luxICDABEG) in pBR322, Apr 10
 pJRD215 Broad-host-range RSF1010-based cosmid vector, Knr Smr Mob+ 5
 pAMS129 8-kb XbaI-SalI fragment with luxR′ luxICDABEG from pJE202 in XbaI-SalI sites of pJRD215, Knr Smr Mob+ This study
 pLAX185 rpoA in pINIIIA1, Apr 15
 pLAD256 rpoA with deletion of sequences encoding C-terminal 73 amino acids of RpoA in pINIIIA1, Apr 15
 pAMS103 lux intergenic region in pUC19, Apr 23
 pAMS1300 luxI promoter in pMP7, Apr 23