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. 2000 Dec;182(23):6774–6782. doi: 10.1128/jb.182.23.6774-6782.2000

TABLE 2.

Oligonucleotides used in this study

Oligonucleotide no. Sequence, 5′–3′a Use
726  TCACCCGGGATCACGAGGTCAGGTTCTTAC Φ(rhaB-lacZ226 construction; upstream
744  CGCGGATCCCCACTGGATGCGCCGAGATCG Φ(rhaS-lacZ309 construction; upstream
896  CGCGGATCCTCTATCGCCACGGACGCGTT Φ(rhaS-lacZ309 construction; downstream
900  CGCCAGGGTTTTCCCAGTCACGA lacZ fusion screening; downstream
1170 CCGGAATTCTTGTGGTGATGTGATGCTCAC Φ(rhaS-lacZ128 construction; upstream
2079 CGCCAGGGTTTTCCCAGTCACGAa Universal sequencing oligonucleotide
2104 GATGGATCCGTGCTTGGCAAACCGCAAAC His6-crp fusion construction; upstream
2105 ATAGGTACCATCAGTCTGCGCCACATCGG His6-crp fusion construction; downstream
2153 CCGGAATTCTTCACGCTGTATCTTG Φ(rhaS-lacZ90 construction
2165 CCGGAATTCTTGTGGTGATGTGATGCTCAC Amplification of CRP site 2 for mobility shift assays
2170 AGCGTGAATTTAGTGGAAATGCGGTGAb CRP site 2 mutagenesis
2172 GTGAGCATACGATCACCACAATTCb CRP site 3 mutagenesis
a

This primer was IRD41 dye labeled for use in a LI-COR automated sequencer. 

b

Regions of oligonucleotides not complimentary to wild-type crp (for site-directed mutagenesis) are underlined.