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. 2010 Jul 16;192(18):4606–4617. doi: 10.1128/JB.00525-10

TABLE 2.

Primers used in this study

Primer Amplified region Sequencea (5′-3′)
Deletion mutants
    23/24KO-Ds-F Downstream of hrtAB GCATTCTAGATCATCACATTCAGCAATGC
    23/24KO-Ds-R TAGCGTCGACATGGCCGACGGAAAAGCC
    23/24KO-Us-F Upstream of hrtAB GACTGTCGACACGAATGTCGCGGATTCC
    23/24KO-Us-F GACTGTCGACACGAATGTCGCGGATTCC
    dtxR-UP1 Upstream of dtxR GGCAGTACTTCAATGCTGAAGATGAGG
    dtxR-UP2 GGCGTCGACGATCCTAGCGCGAAGAGG
    dtxR-DN1 Downstream of dtxR GGCGTCGACGCCCACACTATTCGTATC
    dtxR-DN2 GGCACTAGTAGTACTGACCGAATATCCTTCACC
hrtB promoter fusion
    DIP2324-PO-R hrtB GGATCCGGCCGGTCAGCATAACG
    DIP2324-PO-F Promoter GTCGACGGGTTCCTACGCTGACC −3′
hrtAB cloning
    DIP2323-R CTGAGGATCCGACTAGCACACCAAATTCC
    DIP2324-PO-F(RV) GGCGATATCGGGTTCCTACGCTGACC
    2324P GGCGATATCCCTTACTTTCACAACAAT
    mntP-Rev GGCGATATCTCCTGTTTGACAAACTTG
chrS cloning
    chrS-kin-R GTCGACGGATCATGAAGTCTCCCG
    chrS-wt-F GGATCCGCAGGAGATCTTTTATGC
ChrS C-terminal expression construct
    chrS-kin-ab-F2 CTACCTCTGAACATATGGCAGGCCGG
    chrS-kin-R GTCGACGGATCATGAAGTCTCCCG
dtxR cloning
    DTRB AAAGACATAGGATCCTATTAAAAGCAATC
    DTRS ATCTAATTTGTCGACTTTAGTATTTAGAG
a

Restriction sites are underlined.