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. 2020 Apr 17;86(9):e00106-20. doi: 10.1128/AEM.00106-20

TABLE 4.

Oligonucleotides used for PCR amplification and cloning of CEs identified by a genome sequence searcha

Enzyme ID Oligonucleotide sequence (5′→3′)
Forward Reverse
CE09 GAGCATATGAGCCTGTTTGTTGATCGCATCAG GCGAAGCTTTCATGCGTGAGCGTCCTCTTC
CE10 CGCATATGGATCTGATCATTTTTCTGC CGGAAGCTTGTTGCAGATCAATATTTAC
CE11 ATACATATGCCGGTCCCCGAAAC GACAAGCTTTCAGGCGTGTATTTCAATC
CE12 GCGCATATGGAACCACTTGAACTTGAGGAC GCGAAGCTTCTATTCACTCAGGTAGCTGAGCACAAC
CE16 AGGTCTAGATGGAGGCTACACCTCATG GTGCTCGAGGTACGGGCAGTTGCCGCGATAATC
CE17 GCGCATATGCACACTCTGTTCAAACG GCGAAGCTTTCAGTCCAAGGCCTGC
CE18 GCGCATATGAATAACCTTACGTTACTGCCC GACAAGCTTCGCTTGCGCTTCCAGCC
CE19 GCGCATATGGTGGTCAATCTCTTTCAGC GACAAGCTTCGCTTTTTCCCAACCGCGTG
CE20 GCGCATATGTCACCGCAC GACAAGCTTCGCAAGTCCGAGGCGTTC
a

Restriction endonuclease sites used for directional cloning are underlined.