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. 2011 Mar 24;6(3):e17350. doi: 10.1371/journal.pone.0017350

Table 3. Primers used in this study.

Name Sequence (5′-3′) a Purpose
PR-F AAGGATCCTTTAACCCAGCTTGATAACC Amplification of mphR promoter region
PR-R CGAATTCGGGATCCTCTGCATTTAAGTC
PX-F GTAAGCTTGGAGATAGTCGCACG Amplification of mphX promoter region
PX-R ACGGATCCACACCACATATGATTG
R1-F GCGAATTCAAGTCTTCAACATTAAC Construction of mphR–deletion mutant
R1-R AAGTCGACTTTGAGCAATTGTC
R2-F TGCGTATCGTCCCGTTGTA
R2-R TCGGCTGTGTCCTGTAAAC
N1-F ATGAATTCGCCACGTTGAACAAAC Construction of mphN–deletion mutant
N1-R TTGTCGACGATTGATCATCCTTAAATC
N2-F ATGTCGACAAGCATGGCTACCTG
N2-R TTGGATCCAGCTTGGAATTCGATTG
X1-F GCAGCGACTACTTATGTGC Construction of mphX–deletion mutant
X1-R ATTTGGAAGGCAGAACTCCT
X2-F ATGTCGACTATAGCTTGGGTTATC
X2-R TTGGATCCGTGAATTGATGAAGATG
MphR188-F TCGAGCCATGAGTGATCTGTT Amplification of the 380-bp mphR-mphK intergenic region
MphK207-R GTACTCCATCAAGACATGGTC
M13-fwd CACGACGTTGTAAAACGAC Amplification of the 380-bp mphR-mphK intergenic region
M13-rev GGATAACAATTTCACACAGG
a

Restriction sites for BamHI (5′-GGATCC-3′), HindIII (5′-AAGCTT-3′), EcoRI (5′-GAATTC-3′), and SalI (5′-GTCGAC-3′) are shown in bold and italic.