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. 2009 Dec 18;9:267. doi: 10.1186/1471-2180-9-267

Table 3.

Primers used for genes amplification and sequencing.

Locus Putative gene Product Locus position* Gene size (bp) Sequence length (bp) Primers** Primer sequence 5'-3'
aroC Chorismate synthase 568275 1094 433 43f TGGGGCGAAAGCCACGGTCTG

740r CCTTCACGGCGTTGATCGACA

dnaK Heat shock protein 70 kDa 818851 1910 534 591f CACGCTCGCCTGGAAGACGC

1865r GGGAACGACCAACTCCTGCGT

1777r TCGCTTACGGTCTGGACAAG

gap Glyceraldehyde-3- phosphate dehydrogenase 1259699 1007 578 138f TCTGCGTTATGACAGCGTTC

940r AAGCCCATTCATTGTCGTA

866r GAAGACCGAGGAATGGGAGT

omp25 25 kDa outer membrane protein 2714010 641 390 188f ACGCGGAACTTGCTTTCGTCG

649r GCGCACTCTTAAGTCTCTCG

recA Recombinase A 2079528 1085 490 1f ATGTCTCAGAATTCATTGCGA

988r CTGACGAAGCGTGGTTTCGAT

697r ATACGGCGAATATCGAGACG

rpoB Beta sub-unit RNA Polymerase 2046339 4133 501 457f ATCGTTTCGCAGATGCACCG

1449r GACATACGTTCCTTGATCGCG

1119r TGACGCGATAGATGTCGAAC

trpE Anthranilate synthase 1671911 2195 564 15f TGCGGATAGCGAGATATTCCA

1486r GCCGATGCCTTCAATTCGGT

659r GTTGCCGTGCGAGACCAT

(f) forward primer; (r) reverse primer. Primers in bold were used for gene sequencing in both directions. (*) gene start codon position on the chromosome I sequence of O. anthropi ATCC 49188T (accession number: CP000758). (**) primer denomination corresponded to its hybridization region in the gene according to the complete genome sequence of O. anthropi ATCC 49188T