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. 2012 Jan;80(1):3–13. doi: 10.1128/IAI.05773-11

Table 1.

Primers used in this study

Primer Orientationa Sequence (5′–3′)b Description
P1 F ACCCGGAGGAAGGGATTCACTTAA PG0352 5′RACE inner primer
P2 R GCCCTTTGTAGTCCGGCAAGTC PG0352 5′RACE outer primer
P3 F GAATTCCTGGTTAGTTTTTGGTTTGTG PG0352 promoter conformation
P4 R GGATCCCATTCGAAAACAATTTTATACCG PG0352 promoter conformation
P5 F GCTCTTTCAGCTTGGTATAGG PG0352 upstream region
P6 R AGATCTGACATAACGTCGAGTCTTCGC PG0352 upstream region
P7 F AGATCTACGATCTCTTCGATGTCCGGC PG0352 downstream region
P8 R GACCTACCACGAATATCAACC PG0352 downstream region
P9 F AGATCTAGCTTCCGCTATTGCTTT erm cassette
P10 R AGATCTTTTATCTACATTCCCTTTAGT erm cassette
P11 F CACCGCAAATAATACTCTTTTGGCGA Confirmation of erm insertion
P12 F TGCCGTTGCAGAAAAGCC Confirmation of erm location
P13 R TTGCCGGACATCGAAGAGATCGTC Confirmation of erm insertion
P14 F TTGTCGGTTTCTGTTGGCTC Confirmation of PG0352 deletion
P15 R AAAGCTTTGCCTCATCGC Confirmation of PG0352 deletion
P16 F AGAGCTGTCGCCTGCCTC PG0352 RT-PCR
P17 R CTGTCGGCTCTCCTGCCGTC PG0352 RT-PCR
P18 F GTCGACATGGCAAATAATACTCTTTT Overexpression of PG0352
P19 R CTGCAGTTGCCGGACATCGAAGAGAT Overexpression of PG0352
a

F, forward primers; R, reverse primers.

b

The engineered restriction enzyme sites are underlined.