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. 2008 May 2;190(13):4489–4500. doi: 10.1128/JB.00414-08

TABLE 1.

PCR primers used in this study

E. coli gene Primer sequence (forward; reverse)a
yghB 5′-CGCGCATATGGCTGTTATTCAAGATATCATCGCTG-3′ (NdeI); 5′-CGCGAAGCTTGGGGAAAATCGTCAGGCGTTACAG-3′ (HindIII)
yqjA 5′-GCGCCATATGGAACTTTTGACCCAATTGCTGCAAGCC-3′ (NdeI); 5′-GCGCAAGCTTGCGAAGCGACATGCGAGGTATTTGCATC-3′ (HindIII)
dedA 5′-GCGCTCTAGAGTAGTTACAGCCTGAAAGATGACGAGTAC-3′ (XbaI); 5′-GCGCAAGCTTGAACCGCGGAGTTACTTTTTATTTTGCG-3′ (HindIII)
yabI 5′-GCGCCATATGGGCACATTATGCAAGCATTGCTGGAAC-3′ (NdeI); 5′-GCGCAAGCTTTCCTAAACCCCAACCACTTTACGC-3′ (HindIII)
yohD 5′-GCGCCATATGGACTGGCCTATGGATCTCAATACACTTATC-3′ (NdeI); 5′-GCGCAAGCTTCAATGGTTTTACGCCTGATGATCCGG-3′ (HindIII)
a

Underlining for each primer sequence indicates the site for the restriction endonuclease (given in parentheses) for that sequence.