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. 2008 Aug 29;74(20):6239–6247. doi: 10.1128/AEM.02155-07

TABLE 1.

Synthetic oligonucleotides used in this study as primers or probes

Name Sequence (5′-3′) Experiment(s)a
mcrCf ATGATCGGAAAGTGCACT Northern
mcrCr TCATGCACCTCCTAATGC Northern
mrtDf ATGATGTCAGAAACAGGA Northern
mrtD52r CCGATTACCCTTGGATC Northern
1132-01f CAGATGCAGGATTCCAGTTA EMSA
1132-01r CCGCTTATGCTTCAGTTTTTT EMSA
1132-02b GCATAAGCGGTTATATTCAGATTAATACTGGATAATAACGAGATGTAC EMSA
1132-03f CGAGATGTACAGTATGGCTT EMSA
1132-03r ACTGATGGGGTTATGGGATT EMSA
1132-04b CCCCATCAGTTTTATTAATAAAATAGTAAATTTTATTAATAAATAAATAAAACAAGAGGT EMSA
1132-05b CGAGATGTACAGTATGGCTTGTTCTATAATGAGCTGTGCTCTGGAG EMSA
1132-06b TGCTCTGGAGGTTGGAGGATGAACTTCGGTATAACCTGAAGGTCCATTTCG EMSA
1132-07b GTCCATTTCGAGACATTGGTGATGGATAGCTCCTTCATGAGGTGACCATTT EMSA
1132-08b GTGACCATTTCCATGGATTATCGCTGGCAATCCCATAACCCCATCAGT EMSA
1132-09rc AAATGGTCACCTATGAAGGAG EMSA
1132-10rc CGAAATGGACCTTCAGGTTAT EMSA
1132-11b TAATGAGCTGTGCTCTGGAGGTTGGAGGATGAACTTCGGT EMSA
1132-12b GAACTTCGGTATAACCTGAAGGTCCATTTCGAGACATTGGT EMSA, affinity
1168-01f GTCACTCTCTCTGTGGAGA EMSA
1168-01r AGTATCATCAGCAGGGAGTA EMSA
1168-02f TGATGATACTCTGCTTTGGG EMSA
1168-02r TCTGAATCAAGTCGAAAGCTT EMSA
1168-03b TTGATTCAGAAAGAAATCTTAATTAATTATAATCAAGTTAAATATGCATCGTATACTAA EMSA
1168-04f GTATACTAAGACGGGTGTTTT EMSA
1168-04r TTCCGTATACTAAACATCCAG EMSA
1168-05b TTGATTCAGAAAGAAATCTTAATTAATTATAATCAAGTTAAATATG EMSA, affinity
1168-06b CTTAATTAATTATAATCAAGTTAAATATGCATCGTATACTAAG EMSA
1168-07b AGAAAGAAATCTTAATTAATTATAATCAAG EMSA
1168-08b AGATTCTAATCTTAATTAATTATAATCAAG EMSA
1168-11b AGAAAGAGGTCTTAATTAATTATAATCAAG EMSA
1168-12b AGAAAGAAATCTTGGTTAATTATAATCAAG EMSA
1168-13b AGAAAGAAATCTTAATTGGTTATAATCAAG EMSA
1168-14b AGAAAGAAATCTTAATTAATTATGGTCAAG EMSA
1168-15b AGAAAGAAATCTTAATTAATTATAATCGGG EMSA
126exp10f ATTCATAATACATATGCATAATGGATCTGCAGGTGd Expression
126exp10r GTTAAAAATAGGATCCTCATTCAAGTCCGGCGATGCe Expression
a

Northern, Northern blot analysis; affinity, affinity particle purification of DNA-binding proteins; expression, cloning and expression of IMPDH VII.

b

Oligonucleotides were annealed with their complement counterparts to prepare double-stranded EMSA probes.

c

Oligonucleotide used for PCR with forward primer 1132-03f.

d

The underlined sequence is an NdeI site.

e

The underlined sequence is a BamHI site.