TABLE 2.
Primer sequences used in this study
| Primer use and gene or site targeteda | Primer | Primer sequence |
|---|---|---|
| Construction of lux reporters | ||
| ldtD | pJW5-ldtD(R) | 5′-AAAGTAATTCTTTGCGTGCGGGGCTTT-3′ |
| ldtD | pJW5-ldtD(F) | 5′-AAACTCGAGTGGTACAAAGCTGGGAAGAT-3′ |
| ygaU | pJW5-ygaU(R) | 5′-AAAGAAATTCTACCGGTTTGTTCAGATGC-3′ |
| ygaU | pJW5-ygaU(F) | 5′-AAACTCGAGGGAACCGCTAAGCATGCACA-3′ |
| slt | pJW5-slt70(R) | 5′-AAAGAATTCTCAATGGACTCACGCACGGT-3′ |
| slt | pJW5-slt70(F) | 5′-AAAGGATCCTGCTCATCCAGTGAGTCGGC-3′ |
| Verification of the MCS in pJW15 | ||
| MCS-pJW15 | MCS-pJW15(R) | 5′-CACCAAAATTAATGGATTGCAC-3′ |
| MCS-pJW15 | MCS-pJW15(F) | 5′-GCTTCCCAACCTTACCAGAG-3′ |
| Amplification of gene promoters for EMSA | ||
| degP | PdegP-F | 5′-CGCTTATTCCACAAACTCTCG-3′ |
| degP | PdegP-R | 5′-CGGCTGAGACTTCTTCAGCAACGA-3′ |
| rpoD | PrpoD-F | 5′-CGAAGAACGCCTGGAGC-3′ |
| rpoD | PrpoD-R | 5′-TCACCTGAATGCCCATGTCG-3′ |
| ygaU | PygaU-F | 5′-AAATGCTGTGATGTCGCAGAGG-3′ |
| ygaU | PygaU-R | 5′-GCGTCCCAGAGTTTTTCTCC-3′ |
| ldtD | PldtD-F | 5′-AAATGGTACAAAGCTGGGAGAT-3′ |
| ldtD | PldtD-R | 5′-AAATTTGCGTGCGGGCTTTTTCT-3′ |
| slt | Pslt70-F | 5′-AAATCCTGCGGCAGATAACCAAT-3′ |
| slt | Pslt70-R | 5′-AAATCGGTGATCTGGCGGTATTC-3′ |
| KEIO or deletion verification | ||
| ldtD | KldtD-F | 5′-AAAGTGGCACATTACGGCG-3′ |
| ldtD | KldtD-R | 5′-AAAGAGAGTGTTGCAAACGCAGG-3′ |
| ygaU | KygaU-F | 5′-AAATCGGTAAAGGGTTCGGTTGG-3′ |
| ygaU | KygaU-R | 5′-AAATAAGCTTGAGGCCTGTGACG-3′ |
| slt | Kslt70-F | 5′-AAATCCTGCGGCAGATAACCAAT-3′ |
| slt | Kslt70-R | 5′-AAATCGGTGATCTGGCGGTATTC-3′ |
| cpxA* (cpxA24) | cpxA*-F | 5′-ATGACCGAGCTTCTGGATAGC-3′ |
| cpxA* (cpxA24) | cpxA*-R | 5′-CTTCGCCATCACGGCACGGGAG-3′ |
MCS, multiple-cloning site.