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. 2007 Aug 10;189(20):7244–7253. doi: 10.1128/JB.00605-07

TABLE 2.

Primers used in this work

Primer name Sequence 5′ position Direction, accession no., use
Per-2 GGMGATGAAGTBATTGTWCCRAC 7148 Forward, AJ605741, degenerate primer for amplifying per gene fragment of Ruokola/71-c for a probe
Per-4 GTYTTRTTYCCAAARAARCTAAA 7482 Reverse, AJ605741, degenerate primer for amplifying per gene fragment of Ruokola/71-c for a probe
galU-f GTTGTCATCGACGGGATATG 4700 Forward, AJ605741, plasmid PCR to delete part of galU gene
galU-r ATTGAATCAGGGGCTTATCG 3919 Reverse, AJ605741, plasmid PCR to delete part of galU gene, cloning of the galU upstream promoter
PSL-F7a TATCAACTGCAACTGCAAAG 3454 Forward, AJ605741, cloning of the galU upstream promoter
F7 CTGAATCATTACTTCGAGTG 3550 Forward, AJ605741, cloning of the galU upstream promoter
galF-F ACCGGGCAATCCTATAACTG 5532 Forward, AJ605741, cloning of the gmd upstream promoter
pSL-7B GTTGTAACATCATCCATTGC 6527 Reverse, AJ605741, cloning of the gmd upstream promoter
pSL-7600Ra TGTTGACAATGGCCATATGA 8552 Forward, AJ605741, cloning of the wzm upstream promoter
pSL-6A AATTTATGAAAAGGCATGCC 7528 Reverse, AJ605741, cloning of the wzm upstream promoter