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. 2011 Jun;55(6):2559–2565. doi: 10.1128/AAC.00010-11

Table 2.

Oligonucleotides used in this study

Oligonucleotide useda Sequence (5′ → 3′)
5′pglnA GGGGATCCCATAAAGGCGGGGCGGTC
3′pglnA GGGGATCCCGGGACATCTTCAGCTCCTGAA
glnA1 GCAACCGCCTGTTTCAAAAAATG
glnA2 GGACATCTTCAGCTCCTGAAAAAG
glnAsec1F TAACGTTTGCCCCGCAACC
glnAsec1R CCCCCGCTACGCCGTTTTC
glnAsec2F GGGCGTGCATAGTCATATTC
glnAsec2R GCGTCAAATTCCAAGCCGG
glnAsec3F AAACCGGTTTCAGACGGCAT
glnAsec3R GGACATCTTCAGCTCCTGAA
glnAtrunckf CATGGATCCGATGAATCTGCGGCGATTTG
rmpF CATGTTTCTACAGCGGCCTG
rmpR CGGCAAGATATTACCTAGCCT
16SRTR CATCGGTATTCCTCCACATCTC
16SRTF GTAGGGTGCGAGCGTTAATC
glnARTR GGCTTTGGCGTGTTTGATG
glnARTF TCCGATACCGCGCTCTACTAC
a

Primers with ending letters RTR or RTF were used in qRT-PCR for the 16S rRNA and glnA transcripts.