TABLE 2.
Primers used in this study
| Analysis | Primer
|
|
|---|---|---|
| Sequence | Characteristics | |
| Chromosomal deletion | CGGAATTCAACTGGCGGCGGATCGGCAATTAT | Region A upstream of lmo2537, forward primer |
| GGGGTACCCGCCAACTAGCGGTGCC | Region A upstream of lmo2537, reverse primer | |
| CGGGATCCC GAAGCTGGGACGTTGAAA | Region B downstream of lmo2537, forward primer | |
| AAAACTGCAGACTCACTTATCATGAGCTGCAT | Region B downstream of lmo2537, reverse primer | |
| lmo2537 gene cloning | CCTCTAGAAGGAGGTTCAAAATTGGCTAAAATC | lmo2537, 5′ end |
| CCTCTAGATTACACGATAAAATCTTCTGGGCG | lmo2537, 3′ end | |
| lmo2537 promotor cloning | CGG AAT TCG TTT AGT AGC AGC TCC TGA AGG | Promoter region (260 bp), 5′ end |
| GGG GTA CCT TTT GAA CCT CCT TAT AAA AAA AC | Promoter region (260 bp), 3′ end | |
| RT-PCR | GGACTTAGAACATGGAATAAATATTCGCCG | Within lmo2537, forward primer |
| CTGCGGTGAGCCGTCATAAGTATTAAACGATTG | Within lmo2537, reverse primer | |
| Real-time PCR | GGCGCAAGCAGCTAATCC | Within lmo2537, forward primer |
| GTGACTCTTGATTGCTGCTAAAA | Within lmo2537, reverse primer | |
| AAATGCGGACATCATTCCTAGACT | Within gyrA, forward primer | |
| TTTAACCCGTCACGAACATCAG | Within gyrA, reverse primer | |