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. Author manuscript; available in PMC: 2013 Mar 11.
Published in final edited form as: Phytother Res. 2012 May 23;27(3):390–396. doi: 10.1002/ptr.4738

Table 2.

Primers used for qRT-PCR experiments

Gene Function Locus ID Primer sequence (forward and reverse)
betB betaine aldehyde dehydrogenase SACOL2628 5′-AATTGCTGTTGGTGGTAAACG-3′
5′-TAACGACAGGTCCGAAAACC-3′
dnaK DnaK protein SACOL1637 5′-CCGGTGACAACAAACTTGG-3′
5′-TCAGCAGCATCTTTCAAACG-3′
mmpL MmpL efflux pump, putative SACOL2566 5′-GGAATGACATCTACAGAAGTAGGC-3′
5′-AACTGCTAGTCCAATCATTACGG-3′
purA adenylosuccinate synthase SACOL0018 5′-GAGGTTGGTCGTGAATACGG-3′
5′-TGGGTACTCAGTAATTTCTTTACCG-3′
purM phosphoribosylaminoimidazole synthetase SACOL1080 5′-AATATGGGTATTGGCTATACGG-3′
5′-CACAATATGACCAATTTGATAGGC-3′
rpmI ribosomal protein L35 SACOL1726 5′-TGCCAAAAATGAAAACTCACC-3′
5′-GAGATGTGAAAGCTCTTGAACG-3′
tenA transcriptional regulator, TenA family SACOL2086 5′-TAGGAGCTGACGCATTACGC-3′
5′-CCCATTGTTCTAGTGTCATAGCC-3′
vraR DNA-binding response regulator VraR SACOL1942 5′-AAAGAAGCAATTGCCAAAGC-3′
5′-TGAGTCGTCGCTTCTACACC-3′
vraS histidine kinase sensor SACOL1943 5′-AGTGCCGATGAAAGTTGTGC-3′
5′-TTTTGTACCGTTTGAATGACG-3′
vraX VraX protein SACOL0625 5′-TCGACAGTATCACCATGAAGG-3′
5′-TTTCAGTATCACTAAATGAATCGTCAC-3′