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. 2016 Oct 17;84(11):3206–3219. doi: 10.1128/IAI.00406-16

TABLE 2.

Oligonucleotides used in this study

Oligonucleotide Sequence (5′–3′)a Product size; positions or relevant characteristicb
ermE1-AscI TTGGCGCGCCTGGCGGAAACGTAAAAGAAG 998 bp; amplicon containing the Ermr gene from pVA838
ermE2-XhoI TTCTCGAGGGCTCCTTGGAAGCTGTCAGT
gbpCP1 CCCTCAACACACTCTGCTAA 473 bp; 323 bp upstream to 150 bp downstream of the gbpC ORF
gbpCP2-AscI TTGGCGCGCCCGGTTCTGATGCTTGTGTAT
gbpCP3-XhoI TTCTCGAGGGAGAAATGCGTGTTAGAGA 387 bp; 1,605 bp upstream to 240 bp downstream of the encoding region of gbpC
gbpCP4 CTTACCCATCACAAAAACCA
C1-SacI GGGAGCTCCCCTCAACACACTCTGCTAA 2,139 bp; amplicon containing the encoding region of gbpC for mutant complementation
C2-SphI GGGCATGCAACAAGAACTGCTGCTCAAG
a

Underlined sequences indicate restriction enzyme linkers.

b

ORF, open reading frame.