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. 2009 May 1;75(13):4362–4373. doi: 10.1128/AEM.02521-08

TABLE 2.

Primers used in this study

Primer Sequencea Construct(s) Use
OriVR 5′-gcTCTAGAAGCTTATTAAGGGTTTTG-3′ pSD5MR, pSD5V Replication and oriV assays
RepAC 5′-gcTCTAGATTAATTGAATAAGTTCGC-3′ pSD5MR Replication assay
OriVF 5′-gcTCTAGAGCTCGTTTCTTTAGTGC-3′ pSD5V oriV assay
OriTF 5′-gcTCTAGAGTTCTTGTATCACCAGCC-3′ pSD5T oriT assay
OriTR 5′-gcTCTAGACTTTTTTATTGCTGATGG-3′
RepAN 5′-ccgcGGATCCATGGAGTACCCTATTTTC-3′ pQERA Promoter assay
RepAC 5′-gccccAAGCTTAATTGAATAAGTTCGC-3′
ParSR 5′-AGAATGACCTTGTACCC-3′ Copy no. estimation
ParAN 5′-ATGATAATTTCATTCC-3′
PF 5′-CAAAATCGCTAATAGAGGGTC-3′ pBTK445 detection
PR 5′- GATACCGGAACCGCAACAC-3′
TB11F1 5′-CCAATCACCCTAACCATGTC-3′ Arbitrary PCR
TB11F2 5′-AATCGCTCATTGCTGCTTGC-3′
Arbit1 5′-GGCCACGCGTCGACTAGTCANNNNNN-3′ Arbitrary PCR
Arbit2 5′-GGCCACGCGTCGACTAGTCA-3′
SoxBF 5′-CAAGGGAAAAACACTGGTGAC-3′ Copy no. estimation
SoxBR 5′-CCCTTTACGCCCCCTTTATC-3′
MocoF 5′-ctagTCTAGAGTGTACCTTCGGGTAC-3′ pBTKSM Complementation
MocoR 5′-ctagTCTAGATGAATCCCTTGCTGCG-3′
a

Underlined sequences indicate restriction sites; nucleotides shown in lowercase were added to the 5′ ends of the sites to ensure complete digestion.