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. 2014 Nov 25;14:282. doi: 10.1186/s12866-014-0282-7

Table 2.

Oligonucleotide primers used in this study

Purpose Primer Sequence
Cloning of 400 bp fragment of fucP (Bbr_1742) in pORI19 FucPF TAGCATAAGCTTGGCGAATCGTTCGTATCA
FucPR GATATCTCTAGAGCGCCCCAGTGCTTGAGC
Cloning of 479 bp fragment of lnbP (Bbr_1587) in pORI19 LnbPF TAGCATAAGCTTCACACAGGTATTGGGAGGTTG
LnbPR CTAGTCTCTAGAGTTGTAGGCGCCACCATCC
Cloning of 568 bp fragment of lacZ7 (Bbr_1833) in pORI19 LacZ7F TAGCATAAGCTTCCAGGCCAAGAACTCCAGTG
LacZ7R CATGATTCTAGACAGCTTGGGCAGGTTGAACG
Amplification of tetW TetWF TCAGCTGTCGACATGCTCATGTACGGTAAG
TetWR GCGACGGTCGACCATTACCTTCTGAAACATA
Confirmation of site-specific homologous recombination FucPconfirm TGTTCGCCATGTTCGTTATC
LnbPconfirm GATCACTCTGCATATGGACG
LacZ7confirm GTACCGACATCGACGCGTTC

Restriction sites incorporated into oligonucleotide primer sequences are indicated in italics.