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. 2006 Jul;74(7):4190–4199. doi: 10.1128/IAI.00926-05

TABLE 2.

Oligonucleotides used in this study

Name Nucleotide sequencea Amplimer
ML1up TATGGACGGAGTAACAAGCC LEE O26-1: 1.65-kb amplimer that corresponds to the first fragment of the LEE O26 locus containing direct repeat 1
ML1lp CGTCAATCGTCTGGTAGAACA
ML1upEco TTGGTTTATGGAATCTGGAGTAACAAGCCAAC Same as above with restriction cutting sites for EcoRI and BglII, respectively
ML1lpBgl CGTCAATCGAGATCTGGTAGAACATAATCTTCA
ML2up AGCAGGATTATATCTGATGAT LEE O26-2: 1.45-kb amplimer that corresponds to the final fragment from LEE O26 containing direct repeat 2 and a 500-bp fragment of the LEE O26 integrase
ML2lp ATGGTTGCTGAACGTGTGGATT
ML2upBgl AGCAGGATTAGATCTGATGATGCCAGACTGTAC Same as above with restriction cutting sites for BglII and EcoRI, respectively
ML2lpEco ATGGTTGCTGAATTCCGTGTGGATTATCCACTG
Intup-Bgl GCATTTGCCCGGAGATCTGATTACTGTTTTAATGGAGC 1.19-kb fragment containing LEE O26 integrase; restriction cutting sites for BglII and NcoI, respectively
Intlp-Nco GCGCCATGGGCCTGCTGGTACATCCTAATGG
Intup-Eco GCATTTGAATTCCCGGGATGATTACTGTTTTA 1.19-kb fragment containing LEE O26 integrase; restriction cutting sites for EcoRI
Intlp-Eco GCGCGGAATTCGCCTGCTGGTACATCCTAATGG
DR2up.Eco AGTTCAGCCGAATTCTGAATGCGTTAAAGAGGGTAC 860-bp fragment containing repeat sequence 2; restriction cutting sites for EcoRI
ML2lp-Eco ATGGTTGCTGAATTCCGTGTGGATTATCCACTG
PheUup TTGGTTTATGGACGGAGTAACAA Used to evaluate chromosomal insertion in E. coli K-12
PheUlp GCAACGTGAAGATGTACTGGGAGA Used to evaluate chromosomal insertion in E. coli K-12
DP-ΔInt1 CACAACGAATTCGCATACCTCTTCAGTGC Construction of MG1655Δb4271 mutant located at locus leuX; restriction cutting sites for EcoRI and BglII, respectively
DP-ΔInt2 AGATCTACAAGCAGATGCATACC
DP-ΔInt3 AGATCTGTTTATCAGTCCATTTGAATATG
DP-ΔInt4 GGTTCAGAATTCTGCTGAACAATTGCGATG
a

Restriction sites are indicated in boldface.