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. 2004 Dec;186(23):8058–8065. doi: 10.1128/JB.186.23.8058-8065.2004

TABLE 2.

Plasmids used in this study

Plasmid Relevant genotype or phenotype Reference
pAR81 cat gene from pTP801 ligated into BamHI-digested pTP809; Cmr This study
pAR90 cfp* inserted between SphI and HindIII sites in pJBA27 44
pAR94 PrrnB, P1 containing SacI-XbaI fragment of pSM1690 inserted into pAR90 digested with SacI and XbaI This study
pAR163 Amplification of dsred2.T3 with primers Dsred2d and UDsRed2.T3 and ligation into Xbal-HindIII-digested pAR94; results in replacement of cfp* with dsred2.T3, controlled by PrrnB, P1 This study
pAR176 Amplification of PtetA with primers ar047 and ar048 from pRL27 and ligation into SacI-XbaI-digested pSM1690; results in replacement of PrrnB, P1 with PtetA This study
pAR178 Amplification of cat gene with primers ar059 and ar060 from pAR81 and ligation with ClaI-SalI-digested p15A ori-containing fragment from pSM1690 (amplified by PCR with primers ar057 and ar058) This study
pAR179 Insertion of PrrnB, P1-RBSII-dsred2.T3-T0 containing NotI cassette from pAR163 into the NotI site of pAR178 This study
pDsRed.T3 Encodes a rapidly maturating DsRed.T3 variant 7
pIB264 SphI-ClaI aah-aidA-containing fragment from pIB6 2
pKKJ128 flu gene from E. coli MG1655 in pACYC184 23
pLH44 aah-aidA genes from pIB264 ligated into SphI-ClaI-digested pACYC184 This study
pOS32 gfpmut3b* gene from plasmid pAR176 ligated to XbaI-HindIII-digested pAR179; construct has gfpmut3b* gene under transcriptional control of the E. coli rrnB-P1 promoter This study
pOS33 aidA gene from pIB264 PCR amplified with primers 482 and 483 and ligated into EcoRV-SalI-digested pACYC184 This study
pOS37 aah gene from pIB264 PCR amplified with primers 537 and 541 and ligated into BamH1-XmaIII digested pACYC184 This study
pPKL4 fim gene cluster from E. coli PC31 in pBR322 26
pRL27 mini-Tn5 delivery vector; source of PtetA 29
pSM1690 PrrnB, P1-RBSII-gfpmut3b*-T0-T1 NotI fragment in LOW2; Kmr 49
pTP801 cat gene in BamHI site of pUC19 35
pTP809 pBR322 derivative with multiple cloning site introduced between EcoRI and NdeI sites 35