Skip to main content
. 2012 Feb;194(4):866–874. doi: 10.1128/JB.06341-11

Table 1.

Oligonucleotide primers used in this studya

Primer Sequence (5′–3′) Note
P1 TTGCATCAATACTGGACTC Inactivation, flgJBb, F
P2 TTGAATTTTCAGATCCCTC Inactivation, flgJBb, R
P3 AAGCTTTAATACCCGAGCTTCAAG kan cassette, F
P4 AAGCTTTCAAGTCAGCGTAATGCT kan cassette, R
P5 TATCAGAGGTAGTTGGCGTC aadA cassette, F
P6 TGTCTAGCTTCAAGTATGACG aadA cassette, R
P7 CATATGGAAACCAAAATTAATTCAC Complementation, F
P8 CTGCAGTTATTTACTTTTTTGTAATTG Complementation, R
P9 GGATCCTAATACCCGAGCTTCAAG Complementation, PflgB, F
P10 CATATGACCTCCCTCATTTAAAATTGC Complementation, PflgB, R
P11 ACCCAATATCCTAAAACTTC RT-PCR, bb0776, F
P12 TGGCAGCTGTATAAATTCCT RT-PCR, bb0775, R
P13 ACATCTGGCAAAGCACAAGA RT-PCR, bb0775, F
P14 GTATTGTTGTGCAGTCATTC RT-PCR, bb0774, R
P15 ACTCAAAAGCTATTCAAACT RT-PCR, bb0774, F
P16 TGAATTGTTGCTTTTTACCT RT-PCR, bb0773, R
P17 CACAACAAGAATAAATGATG RT-PCR, bb0773, F
P18 GTTGAAGCTTTGTTTGTTTG RT-PCR, bb0772, R
P19 TGGAGGAAATTGATGGAAAC RT-PCR, bb0772, F
P20 TTAAATCGGCAAGGCCAAAG RT-PCR, bb0858, R
P21 GCCTTGCCGATTTAATTTAC RT-PCR, bb0858, F
P22 TAGCTTGTGTTCTCTTACTG RT-PCR, bb0771, R
P23 TCATCTGCTATGATTATGCCACC qRT-PCR, flaA, F
P24 AGAATAAGCATATTCCATGCCAT qRT-PCR, flaA, R
P25 CATATTCAGATGCAGACAGAGG qRT-PCR, flaB, F
P26 CCCTGAAAGTGATGCTGGTGTG qRT-PCR, flaB, R
P27 TTCTCGCCCTACTGATGCTC qRT-PCR, flgE, F
P28 CCGTTGCCACTAACTCCAAG qRT-PCR, flgE, R
P29 AACAGGAATTAACGAGGCTG qRT-PCR, eno, F
P30 AAATTGCATTAGCACCAAGC qRT-PCR, eno, R
P31 CACCATGGAAACCAAAATTAATTCAC rFlgJBb, F
P32 TTTACTTTTTTGTAATTG rFlgJBb, R
a

The underlined sequences are engineered restriction cut sites for DNA cloning. F, forward; R, reverse.

HHS Vulnerability Disclosure