TABLE 2.
Oligonucleotide primers used in this work
| Oligonucleotide | Sequencea |
|---|---|
| D-248F | GCGCGCGCTCTAGATGATCTGTCAGACTCAATC |
| D-187F | GCGCGCGCTCTAGATATAAAATTAAATAATTCTG |
| D-667F | GCGCGCGCTCTAGAATATCTAAAGCCTCCGTGTA |
| D+26R | GCATGCGCGGATCCGTGAAGCTTGCATTTATCTT |
| MctF | CGTGTTCTAAAATCTTCTATGTTTAT |
| MagR | ATAAACATAGAAGATTTTAGTTCACG |
| NlbF | CTGGCCGAAAAAGATGCTAC |
| NlbR | GCCTCTTCCAGCTTTTCCTT |
| PE-F | GCTTTGGACGCAGTGTCAACAGCA |
| PE-R | GGGACAGCAGGATAGTACTGCTG |
| GP.F | GTGCCTATCCGAAATTGAAATG |
| GP.R | TTGGTACAAAAGGAATTGCAAA |
| GD.F | CGAACCATATCATGTTTATATA |
| GD.R | TATATAAACATGATATGGTTCG |
a
The underlined sequences are the sites for restriction enzymes used for cloning of the resulting PCR products.