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. 2016 Aug 22;60(9):5189–5197. doi: 10.1128/AAC.00539-16

TABLE 1.

Nucleotide sequences of the primers used in this study

Primer Nucleotide sequencea Comment
gyrB_Fw 5′-GCACCAGGAAGAAAGATGTCC-3′ Amplification (nucleotide positions 5084–5104)b
gyrA_Rv 5′-TTCCTCCTCAGATCGCTACG-3′ Amplification (nucleotide positions 9867–9848)b
gyrA_cln_Fw 5′-ATGACAGACACGACGTTGCCGCCTG-3′ Cloning, bp 1–25 of gyrA
gyrA_cln_Rv 5′-CATCGTCGTCGCTCGAGCCTGATTAA-3′ Cloning, inserted XhoI site
gyrB_cln_Fw 5′-ATGGGTAAAAACGAGGCCAGAAGATC-3′ Cloning, bp 1–25 of gyrB
gyrB_cln_Rv 5′-TGCATCTCCTGCAGGATGTCAACCG-3′ Cloning, inserted SbfI site
Mut_GB538_Fw 5′-GGTGCTAAAGGACACCGAAGTTCAG-3′ Mutagenesis
Mut_GB538_Rv 5′-CGGTCGATGCGCGCTTTC-3′ Mutagenesis
Mut_GB540_Fw 5′-AGAACACCGACGTTCAGGCGATC-3′ Mutagenesis
Mut_GB540_rv 5′-TTAGCACCCGGTCGATGC-3′ Mutagenesis
a

The restriction enzyme site or mutated nucleotide is underlined.

b

Nucleotide position on chromosome of M. tuberculosis H37Rv (accession no. NC_000962.3).