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. 1998 Jan;180(1):171–174. doi: 10.1128/jb.180.1.171-174.1998

TABLE 1.

Strains and plasmids used in this study

Strain or plasmid Relevant genotype and description Source and/or reference
Strains
 MC4100 FaraD139 Δ(argF-lac)U169 rpsL150 relA1 flbB5301 deoC1 ptsF25 rbsR 4
 MH1160 MC4100 ompR101 9
 LM101 MC4100 Δ(ompR-envZ)::Kanr 18
 FR247 MC4100 ompR101 Φ(ompC′-lacZ+)10–25 envZ247 zhf37::Tn10 (λpSG10) 22
 CYL304 MC4100 ompR101 envZ247 zhf37::Tn10 This study
 MS10095 JM107 zad::Tn10 pcnB80 17; M. Singer
 CYL302 MH1160 zad::Tn10 pcnB80 This study
 CYL303 LM101 zad::Tn10 pcnB80 This study
 CYL305 CYL304 zad::Tn10 pcnB80 This study
Plasmids
 pACYC177 5
 pUC19 27
 pLAN701 ompR+ cloned into pACYC177a This study
 pLAN702 ompRD55E cloned into pACYC177b This study
 pLAN801 ompR+ cloned into pUC19a This study
 pLAN802 ompRD55E cloned into pUC19b This study
a

A 1,050-bp EcoRI-HindIII PCR-generated DNA fragment containing the ompR+ sequence from position −127 to +923 from the start point of ompR transcription. 

b

A 1,050-bp EcoRI-HindIII PCR-generated DNA fragment containing the ompR+ sequence with the codon at position 55 changed from GAT to GAA to generate the ompRD55E allele.