TABLE 1.
Oligonucleotide primers used in this study
Primer | Sequence (5′→3′)a | Purpose in this studyb |
---|---|---|
p11 | ACTACGCCGACAACACCAAGTTCG | Probe for narG |
p12 | TGTTCTGCTGGGTTCGGTCGTGGTA | Probe for narG |
p13 | TGCTGCTGGTGGCGACCGCGCTGGTCGCGT | Cloning narX |
p14 | GCGCGGACTTGTTCGACGAGTAGACGTGT | Cloning narX |
p19 | GTGAGCGGGTACCAATTTCACACAGG | Cloning lacZ |
p20 | GGCCTGCCCGGGTATTATTATTTTTG | Cloning lacZ |
p23 | GGTGATCGCCATGGTCGACCTGCAGG | Cloning aphI |
p24 | TAATGCTCTGCCATGGTTACAACCAA | Cloning aphI |
p27 | ATGCGCCTCGGTGCTGCTGACCTACCCGAA | Probe for narX |
p28 | GGATCGGCACGGCGCAGCTCAGAGACCGTG | Probe for narX |
p46 | CTGGATTGCGGATCTAGAGCGAACCCTCAA | Construction of pMP101 |
p47 | ACGGTCACGGGGGTACCCTCCTCGTCATGA | Construction of pMP101 |
p48 | TCCCCTTTCTAGAGGCGACCAGGCTCAGCT | Construction of pMP102 |
p49 | TCATCGACAGGTACCGGGGTCTCGGACTCC | Construction of pMP102 |
p51 | CAGCTCCTGGATCCGGCTGCCGGTCCGTGG | Cloning narK2 |
p58 | ACTCGAGTGGCGAACGGGTGAGTAACACGT | RT-PCR of 16S rRNA |
p59 | AGGCCGTCACCCCACCAACAAGCTGATAGG | RT-PCR of 16S rRNA |
p60 | ACTACGCCGACAACACCAAGTTCGCCGACG | RT-PCR of narG |
p61 | AGCGGCGCACATAGTCGACAAAGAACGGAA | RT-PCR of narG |
p62 | ATTGGTGGGACGTGGTGTGGCAATGCGCCT | RT-PCR of narX |
p63 | GACCGTCGATGTGGGCCAGCAATTCCTCTG | RT-PCR of narX |
p66 | TGCTTCGTGATGCACCCTACTTTCGGCCCA | RT-PCR of narK2 |
p67 | CCGCCGAACACGATCGCGTACAGAAACGAC | RT-PCR of narK2 |
p68 | CCAAGTCGGACAAGCTTCGGGCGACCGAGA | Cloning narK2 |
Mismatches used to create restriction sites are indicated by underlining.
RT-PCR, reverse transcriptase PCR.