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. 2008 Dec 12;191(5):1688–1694. doi: 10.1128/JB.01551-08

TABLE 1.

Oligonucleotides used in this study

Oligonucleotidea Sequence (5′-3′) Application
FtsHP CGTTTGTGAGCCGGAATTACCGC Primer extension analyses
ldhDF ACGCCCAAGCTGATGTTATATC qRT-PCR
ldhDR AGTGTCCCACGAGCAAAGTT qRT-PCR
gyrAF CATGCGGTTAGGCGATGAT qRT-PCR
gyrAR ATCGGCGTTGACGGTTTG qRT-PCR
FtsH1F TTACGGTCTTGACTATGCAGAACGCTATCGGAACT Gel mobility shift assay
FtsH2F TCGATGAAGGAGGCACATATGAACAATCGACGCA Gel mobility shift assay
FtsH1R GCTGGATACTAACGTTTTTAACGTTATTCTTATCTAATTG Gel mobility shift assay
FB1ctsR ATCTCGAGTTAAAATCCTGCGGTTAGTG ctsR chromosomal deletion
RB1ctsR* GACTTTGCATGTGCTTCACC ctsR chromosomal deletion
FB2ctsR* CGGGCCCGGATAATTATCGG ctsR chromosomal deletion
RB2ctsR* TCATCCGTAATCGTAACCCG ctsR chromosomal deletion
FBctsR* TGAACCGGCAACAAGGCATG ctsR chromosomal deletion
CtsRrtF AATTTGGTCGATGATGCTGATG qRT-PCR
CtsRrtR TAAGTCCCGGTCCGTTAATCC qRT-PCR
CtsR1 GGTGGTCTCCCATGCAAAGTCAAAATATC ctsR overexpression
CtsR2 CTCCTCGAGGCTTTCGTAACGCAAGTGGTT ctsR overexpression
CatF TCAAATACAGCTTTTAGAACTGG ctsR chromosomal deletion
CatR CCAGTAAATGAAGTCCATGGA ctsR chromosomal deletion
ftsHKOF ATGGTACCGGACTTATTCGAACAAGCTAAG ftsH disruption
ftsHKOR TAGGATCCGTAAGCTGCTTGTTGGTTG ftsH disruption
pUCeryF CCAGGCTTTACACTTTATGC ftsH disruption
pUCeryF TGGAAAGTTACACGTTACTAAAG ftsH disruption
ftsHrtF GCAGCTACCTTCGAAGAATCCA qRT-PCR
ftsHrtR GGGAAACTTGGTTCAGCAACA qRT-PCR
ftsHF AAAACTGCAGAATCGACGCAATGGAC ftsH disruption
ftsHR GCTCTAGACGCTCATAACCGAATTAACG ftsH disruption
a

Asterisks indicate 5′-phosphorylated oligonucleotides.