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. 2010 Jun;161(5-3):346–354. doi: 10.1016/j.resmic.2010.04.003

Table 3.

Primers used.

Name Primer Description Reference
FRA 5′-GTA AAG CTG CAG ATG AAG TGA TCG-3′ (PstI) FRA and RRA amplify the full-length B. fragilis recA BF638R1245 gene. Restriction enzyme sites (in brackets) are underlined. This study
RRA 5′-GGG CAT GCC TAT CGA GTT GG-3′ (SphI) This study
FBRT 5′-CCG GCT ATG ATC GGT GCC-3′ FBRT and RBRT amplify the intergenic region between BF638R1248 and BF638R1246/7. This study
RBRT 5′-CGG CTT TAC GTA GCT CTG CG-3′ This study
RART 5′-CGT GGA TGG CCA GTG TCG-3′ FRA and RART amplify the intergenic region between BF638R1246/7 and BF638R1245. This study
M13F 5′-CGC CAG GGT TTT CCC AGT CAC GAC-3′ M13F and M13R in combination with gene-specific primers allow verification of mutation in B. fragilis 638R recA. Val Abratt Yanisch-Perron et al., 1985
M13R 5′-GAG CGG ATA ACA ATT TCA CAC AGG-3′ Val Abratt Yanisch-Perron et al., 1985
RIF 5′-CAG GTT CGA TAG CAC TGA ATG C-3′ RIF and RIR amplify an internal fragment of the B. fragilis recA BF638R1245 gene; used for the mutation of recA This study
RIR 5′-CGG ATT ACC GAA CAT TAC ACC G-3′ This study