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. Author manuscript; available in PMC: 2011 Apr 1.
Published in final edited form as: Mol Microbiol. 2010 Feb 28;76(2):393–408. doi: 10.1111/j.1365-2958.2010.07103.x

Table 1.

Oligonucleotides used in this study

Primer Description Sequence
pCAEV1 Upstream (+) pCAEV1 vector construction CAGAATGAGTTACTTCTGGATGG
pCAEV1 OspC 5′ (−) BspEI/MluI PCAEV1 vector GTACGCGTTTTTCCGGAATTATTACAAGATATAA
pCAEV1 OspC 3′ (+) BspEI PCAEV1 vector TCCGGATCAATATTATAAGATTAATTTGTTTTAAA
pCAEV1 BBB 21 3′ (−) AatII PCAEV1 vector GACGTCATCTCACATAAAACCAAAGAAACTAC
Spec/Strep (+) SalI PCAEV1 vector GTCGACTAATACCCGAGCTTCAAGGA
Spec/Strep (−) AatII PCAEV1 vector GACGTCATTATTTGCCGACTACCTTGG
pCAEV1 Downstream (+) SalI PCAEV1 vector GTCGACTTTAAAAAGTTGTTAAATAGACTTAACT
pCAEV1 Downstream (−) MluI PCAEV1 vector ACGCGTGGATATATGCAATCTTTAGTCCAG
Insert type A (+) BspEI Amplification of insert TCCGGAAAAGATGGGAATACATCTGCA
Insert type A (−) BspEI Amplification of insert TCCGGATTAAGGTTTTTTTGGACTTTCTG
Upstream confirm (+) Transformation confirmation CCTACGTTGTGATGAGACTTGATTT
Spec/strep 3′ (+) Transformation confirmation GGCGAGATCACCAAGGTAGTC
Insert sequencing (+) OspC sequence TAAAAAGGAGGCACAAATTAATG
Deletion upstream (+) Deletion vector construction GCAACAATCCAGTGTTTACAAAAACG
Deletion upstream (−) Deletion vector construction ACCGGTTCTGACGTCTAATTTGTGCCTCCTTTTT
Deletion downstream (+) Deletion vector construction GACGTCGTTGTGGCAGAAAGTCCAAAAAAACC
Deletion dow nstream (−) Deletion vector construction ACCGGTGCTGTTTAACGATTTATTTGATACTTTG
OspC (+) LIC Amplification of OspC for GACGACGACAAGATTAATAATTCAGGGAAAGAT
OspC (−) LIC Amplification of OspC for GAGGAGAAGCCCGGTTTAAGGTTTTTTTGGACT
OspC E61Q/E63Q (+) Mutagenic primer GTGAAACAGGTTCAAGCGTTG
OspC E61Q/E63Q (−) Mutagenic primer CAACGCTTGAACCTGTTTCAC
OspC K60Y (+) Mutagenic primer CAACGCTTCAACCTCATACAC
OspC K60Y (−) Mutagenic primer GTGTATGAGGTTGAAGCGTTG
OspC E61Q (+) Mutagenic primer GTGAAACAGGTTGAAGCGTTG
OspC E61Q (−) Mutagenic primer CAACGCTTCAACCTGTTTCAC
OspC E63Q (+) Mutagenic primer GTGAAAGAGGTTCAAGCGTTG
OspC E63Q (−) Mutagenic primer CAACGCTTGAACCTCTTTCAC
FlaB q-PCR primer (+) q-PCR primer CAGGTAACGGCACATATTCAGATGC
FlaB q-PCR primer (−) q-PCR primer CTTGGTTTGCTCCAACATGAACTC
Nid1 q-PCR primer (+) q-PCR primer CCAGCCACAGAATACCATCC
Nid1 q-PCR primer (−) q-PCR primer GGACATACTCTGCTGCCATC