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. 2011 Oct;157(Pt 10):2831–2840. doi: 10.1099/mic.0.051706-0

Table 2. Oligonucleotides used in this study.

Functional restriction-enzyme sites added to the primer are underlined. The sequence for one copy of the bmpB terminator is indicated in bold. The sequence for the B. burgdorferi codon usage-optimized FLAG epitope is indicated in italics. The engineered ATG sequence in primer 5 is indicated in lower-case letters.

Number Name Sequence 5′–3′
1 bmpB termX3 FWD CCCCCCCAATTGCTTTTTTGGCTGGCTATATTGCAGCCAAAAAAAGCTTTTCGCTTTTTTGGCTGGCTATATTGCAGCCAAAAAAAGCTTTTCGCTTTTTTGGCTGGCTATATTGCAGCCAAAAAAAGCTTTTCGGAATTCCG
2 bmpB termX3 REV CGGAATTCCGAAAAGCTTTTTTTGGCTGCAATATAGCCAGCCAAAAAAGCGAAAAGCTTTTTTTGGCTGCAATATAGCCAGCCAAAAAAGCGAAAAGCTTTTTTTGGCTGCAATATAGCCAGCCAAAAAAGCAATTGGGGGGG
3 pncA 5′ EcoRI N CGGAATTCCTATGCTATCCCCTTGTTCAAGTC
4 pncA FLAG XbaI 3′ GCTCTAGATTATTTATCATCATCATCTTTATAATCTATATTAAGCTTACTTTGGCTG
5 pncA 5′ EcoRI A CGGAATTCatgGCACTTATTTTAATAGATATAC
6 pncA 5′ EcoRI B CGGAATTCATGCCAGTATCTAACAGTAATG
7 flaB prom 5′ EcoRI CGGAATTCTGTCTGTCGCCTCTTGTGGCTTCC
8 flaB prom 3′ EcoRI CGGAATTCGATTGATAATCATATATCATTCC