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. 2013 Mar;79(5):1436–1443. doi: 10.1128/AEM.03306-12

Table 2.

primers used in this study

Primer Description Sequencea
Forward Reverse
Δdpr-F1 Upstream of dpr for Δdpr AAGCCTATCCACAGTGT CAGTCGAGGATCCTCCTTAAAAAATATTCTT
Δdpr-F2 Downstream of dpr for Δdpr GCTGACCTAGTAAAAGACAATCTGGATGTT CATCTTCCAAAATATTGGT
Δsod-F1 Upstream of sod for Δsod GTCTTCAGGGAGAAGATG CAGTCGAGGATTCATTTCCTCTTTTCTTTT
Δsod-F2 Downstream of sod for Δsod GCTGACCTAGTCTGTTGCTCGTCTTTATG AACGAGCTATTCCATTCT
ΔahpCF-F1 Upstream of ahpC for ΔahpCF GAATTGTGGAAAGTCGC CAGTCGAGGATACACTTGTCCTCCTTCT
ΔahpCF-F2 Downstream of ahpF for ΔahpCF GCTGACCTAGTGCTTTAGGTGCCTTTGA TCGGAGTTCTCTCAACT
ΔperR-F1 Upstream of perR for ΔperR TTGAGTGCTTGGTTGAAT CAGTCGAGGATTTGACTCCTTCGTTATTC
ΔperR-F2 Downstream of perR for ΔperR GCTGACCTAGTATTTGTCCAGACTGTCAA GCCAATGTTCATGCTTTT
perR-compl.-F1 perR complementation TGCGGATCCTTGATGATGCTAGGCAC TCTTTGTTTCTTACCTCCTATTTCCCATAT
Emr Erythromycin resistance gene for deletion ATCCTCGACTGGAAGCAAACTTAAGAGTG ACTAGGTCAGCTTATTTCCTCCCGTTAAA
Spcr Spectinomycin resistance gene for complementation, double deletion ATCCTCGACTGATCGATTTTCGTTCGTGA ACTAGGTCAGCTTCCACCATTTTTTCAATTT
ftf-N-terminal Complementation ATCTCGAGTTTACTAAGTTCAACAATGG AAGTCGACCCACCAATAACATTCCAAT
ftf-C-terminal Complementation AAGAAACAAAGAAAGCTCATCATGTTTCAAC CGGCCGCGGTTCGTCTTGTTTCTCTCA
ΔΔperR-F1 Upstream of perR for double deletion TTGAGTGCTTGGTTGAATb CAGTCGAGGATTTGACTCCTTCGTTATTCb
ΔΔperR-F2 Downstream of perR for double deletion GCTGACCTAGTATTTGTCCAGACTGTCAAb GCCAATGTTCATGCTTTTb
dpr Primers for quantitative PCR for dpr GTGGTTCAGGCTTCCTTTAT ACTGTTTCTTCAAGTCTGGA
sod Primers for quantitative PCR for sod GTTTTGGCTCAGGTTGGGCT ATAGTTTGGACGAACATTAC
ahpC Primers for quantitative PCR for ahpC TGGTTTAGCACAACGTGGAA AGGGCAAACTTCTCCTGGAT
sloR Primers for quantitative PCR for sloR ACTGTCTCTGATGTGTTTGT TCAACAAATATACTCCCATC
gyrA Primers for quantitative PCR for gyrA TCTCGCTGGACTTGTCACTG CATCTAGGCGCATCACTTTG
a

Restriction enzyme sequences are underlined.

b

Same primer as ΔperR-F1 or ΔperR-F2.