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. 2008 Feb 1;74(6):1954–1958. doi: 10.1128/AEM.02294-07

TABLE 1.

Oligonucleotides used for PCR amplifications

Primer name Restriction site Nucleotide sequencea
Deletion analysis
    TBT1F HindIII 5′-aggtaaagctt-TGCACCCAGAACGCGTGAAT-3′
    TBT1R HindIII 5′-acagcaagctt-TTACGAGTGGTATTTGACGATGTTGGC-3′
    TBT2F NruI 5′-gagtatcgcga-TGCACCCAGAACGCGTGAAT-3′
    TBT2R EcoRI 5′-agttgaattcctcctcct-GCACTGGCCTGTAATTGCGTGA-3′
    TBT3F NruI 5′-tattatcgcga-TCACGCAATTACAGGCCAGTGC-3′
    TBT4F NruI 5′-ccaagtcgcga-TAATGAACGCCCAACCGAACC-3′
    TBT5F NruI 5′-actcttcgcga-TGATGACGATTCTCCAGAAACCCA-3′
    TBT6F NruI 5′-agttttcgcga-GCGTAGTAATTTTAGCGGAGGCTG-3′
    TBT7F NruI 5′-aatgttcgcga-TCATTTACGCTGCTGAGGCTGG-3′
    TBT8R EcoRI 5′-agttgaattcctcctcct-CCAGCCTCAGCAGCGTAAATGA-3′
Complementation of ygaVP deletion
    TBT9R EcoRI 5′-tattgaattcctcctcct-CATGCGGCGAAATGGTTGTC-3′
    TBT10R EcoRI 5′-aaaaaagaattccctcctta-GTCCGGCGTCGCTTCTCAA-3′
a

Lowercase letters indicate linker sequences. Underlined letters indicate the restriction sites. Boldface letters indicate a Shine-Dalgarno sequence added, when necessary, for luxC translation.