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. 2011 Nov;77(21):7576–7585. doi: 10.1128/AEM.06107-11

Table 2.

Oligonucleotides used in this study

Primer Sequence (5′ → 3′)a Function
celB-qF1 ATTTGGCCCGTGCTTACG qRT-PCR, celB
celB-qR1 TTTGGCAAACCTGCAAATAGG
QptcC-F CGTGTTCGGTATTGCTTACG qRT-PCR, ptcC
QptcC-R TGTTAAACCAGCGGGTACTC
qBglS-F TACACCGCAGTATGCTAAGG qRT-PCR, bglS
qBglS-R TTGGCCGACTTCAAGAGTTC
Tuf-F GGTAGTTGTCGAAGAATGGAGTGTGA qRT-PCR, internal control
Tuf-R TAAACCAGGTTCAATCACTCCACACA
celB-1 AACTCtAGATGGCCTTTGTA (XbaI) Cloning and disruption of celB
celB-4 gAagAtctAAGACAGCCGCTCC (BglII)
a

Changes introduced to generate restriction sites (underlined and shown in parentheses) are indicated in lowercase.