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. 1999 May;43(5):1156–1162. doi: 10.1128/aac.43.5.1156

TABLE 1.

Oligonucleotide primers used in this study

Primer Orientation when used as primer Positionsa Base sequence
VGYR-1 Sense GyrA, 41–46; ParC, 43–48 5′-T(A/C/G/T)AA(A/G)CC(A/C/G/T)GT(A/C/G/T)CA(C/T)(A/C)G-3′
VGYR-2 Sense GyrA, 57–62 5′-AA(C/T)GA(C/T)TGGAA(C/T)AA(A/G)(G/C)C-3′
VGYR-3 Sense ParC, 78–83 5′-AA(A/G)TA(C/T)CA(C/T)CC(A/C/G/T)CA(C/T)G-3′
VGYR-4 Antisense GyrA, 124–119; ParC, 127–122 5′-TC(A/C/G/T)GT(A/G)TA(A/C/G/T)C(G/T)CAT(A/C/G/T)GC-3′
GYRAS1 Antisense 564–534 5′-CGGTGTAACGCATTGCCGCAGCAGAGTCGCC-3′
GYRAS2 Antisense 395–365 5′-GGCTGATTTTTTATATGGTTTGTTCCAATCG-3′
GYRS1 Sense 365–395 5′-CGATTGGAACAAACCATATAAAAAATCAGCC-3′
GYRS2 Sense 534–564 5′-GGCGACTCTGCTGCGGCAATGCGTTACACCG-3′
PARAS1 Antisense 465–434 5′-GGAGCACCCCAGTTTCCCTGACCATCAACCAG-3′
PARAS2 Antisense 441–408 5′-TCAACCAGTGGGTAACGGTAAGAGAATGGTTGCG-3′
PARS1 Sense 403–436 5′-AATGGCGCAACCATTCTCTTACCGTTACCCACTG-3′
PARS2 Sense 434–465 5′-CTGGTTGATGGTCAGGGAAACTGGGGTGCTCC-3′
GYRCL1 Sense 11–42 5′-AAATATAGTCAGTTTCAGAAAGATATGGGATG-3′
GYRCL2 Antisense 2895–2864 5′-TGATGAAGATACAAAAAAGACGAGAATTTTGC-3′
PARCL1 Sense 11–40 5′-ATCGACGACTCTGAAGCCACTATGGAAATG-3′
PARCL2 Antisense 2523–2495 5′-GTTGGTATCATTCGTAAAGGCAAGGAATG-3′
GYRM1 Sense 365–386 5′-CGATTGGAACAAACCATATAAA-3′
GYRM2 Antisense 564–545 5′-CGGTGTAACGCATTGCCGCA-3′
PARM1 Sense 293–312 5′-CTTGGTCTTTCGGCATCAGC-3′
PARM2 Antisense 506–487 5′-CTTCGGTATAACGCATTGCC-3′
Cassette C1 5′-GTACATATTGTCGTTAGAACGCGTAATACGACTCA-3′
Cassette C2 5′-CGTTAGAACGCGTAATACGACTCACTATAGGGAGA-3′
a

The positions of VGYR-1, VGYR-2, VGYR-3, and VGYR-4 degenerate primers correspond to amino acid residues of E. coli GyrA and ParC (Fig. 2 and Fig. 3). The positions of other primers correspond to base positions of the V. parahaemolyticus gyrA and parC genes deposited in GenBank (accession no. AB023569 and AB023570, respectively); primer designations starting with GYR and PAR indicate primers for the gyrA and parC genes, respectively.