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. 2008 May 2;74(13):4101–4110. doi: 10.1128/AEM.00061-08

TABLE 1.

Primers used in this study

Primer and use Sequencea (5′ to 3′)
Initial identification of vtpA and vthA
    HA5′deg1 GGNCCNGGNGGNAAYCARAARAC
    HA3′4 GCCCGCTTTGACATACAGATCCGCATCGCCC
    Cy5′2 CGCGTCAATGTGGCACAAATGCGCTCGGTACAATC
    Cy3′2 TAGGCCCCAAACTTGGTTCCAACTGCCGTGACAGC
Inverse PCR
    5HapOut GTCCGTACCGAAGTTGTATTG
    3HapOut GACAGCAAACAGCACGTTTGA
    5CytOut GCCAATGTACGTGCGGCGGTTCGCCCAGCTTTGG
    3CytOut GCAACGACAGGATGGTCAATTCCACGTACGGTTCG
pBAD expression cloning
    5hapexp GAGGAATAATAAATGAAACAACGTCAAATGCTTTG
    3hapexp TTAGTCTAATCTTAGTGTCACGC
    5cytexp GAGGAATAATAAATGAAAACTTCTACAATTTTCAC
    3cytexp TTAAAGTTTGATTTGCTGTAGTG
vtpA internal deletion
    5HapDel GGGGGGCGGCCGCCAATACAACTTCGGTACGGAC
    3HapDel GGGGGACTAGTTCAAACGTGCTGTTTGCTGTC
a

N = A, G, C, or T; Y = C or T; R = A or G.