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. 2016 Aug 30;82(18):5621–5630. doi: 10.1128/AEM.01201-16

TABLE 2.

Primers used in this study

Primer DNA sequence (5′ to 3′)a Purpose
pBBRdmt02-F GGGGTACCCATGTTGTCGGGGTGAAGGAAAGTG (KpnI) Amplification of a fragment containing the methyltransferase gene from scaffold 02 for functional study in strain DC-6
pBBRdmt02-R GCTCTAGATGTCCTGGGCCGCAAGGGCGAGTT (XbaI)
pBBRdmt02c-F CGGGGTACCCAATGGCGGCCGCCCTGATGCTC (KpnI) Amplification of a fragment containing the methyltransferase gene cluster from scaffold 02 for functional study in strain DC-6
pBBRdmt02c-R CCGGAATTCTGGCTTCGGCATCGCCACCGAATGC (EcoR I)
pBBRdmt66-F CGGAATTCGGGTCAGGGCGCGGCCGCTAGG (EcoR I) Amplification of a fragment containing the methyltransferase gene from scaffold 66 for functional study in strain DC-6
pBBRdmt66-R GCTCTAGAGCACGGCGAGAATAACCCCGAAGCA (XbaI)
pBBRdmt66c-F CTAGTCTAGACGTTGCAGCTCATCAACACCCACGA (XbaI) Amplification of a fragment containing the methyltransferase gene cluster from scaffold 66 for functional study in strain DC-6
pBBRdmt66c-R CCCAAGCTTTCAAGTCCGCCATCAGGAGCGAA (HindIII)
pET-dmt02-F GGAATTCCATATGAAGAGCCCATTGATGAAATATCGG (NdeI) Amplification of the methyltransferase gene from scaffold 02 for expression in Escherichia coli
pET-dmt02-R CCGCTCGAGTCAGTCTTTCTTGATGACCTTCTCG (XhoI)
pET-dmt66-F GGAATTCCATATGGTGCGGTCGGTTCAGGA (NdeI) Amplification of the methyltransferase gene from scaffold 66 for expression in Escherichia coli
pET-dmt66-R CCGCTCGAGGAGCGTCGCGCGGACCCGGC(XhoI)
RTdmt-F GCCTTTCATTCCTGCCGAGTTCA Amplification of a 525-bp fragment of dmt by RT-PCR
RTdmt-R ATGCCATGCCGCAGGATGTGAACGC
RTmetF-F CGGCGCTCATCGTCACGCAATT Amplification of a 301-bp fragment of metF by RT-PCR
RTmetF-R AAAGGGTAGAAGTGCAGGCGGACAT
RTpurU-F TTGACCATTGCCTGGGTGACCTGCT Amplification of a 540-bp fragment of purU by RT-PCR
RTpurU-R TTCAGGAAGACCCGGCCCTCCAGAT
RTdhc-F CATAAAGCCTGCGAAGGACGTGGA Amplification of a 166-bp fragment of dhc by RT-PCR
RTdhc-R TCGACTTTCCGATCACCACAGCG
RTdmt-metF-F TTTACACCAGCGACGCAATGAA Amplification of a 1,167-bp fragment of dmt-metF-spanning region
RTdmt-metF-R CTGGCAATCAACTGCATGCTATCGG
RTmetF-purU-F GTCCGCATCCGTGCTGAGCAAATAT Amplification of a 604-bp fragment of metF-purU-spanning region
RTmetF-purU-R GAACGGGACGCCACGGAGCGATGAG
RTpurU-dhc-F ATCGCCCAGGATACCGAGGTCGT Amplification of a 663-bp fragment of purU-dhc-spanning region
RTpurU-dhc-R TCGACTTTCCGATCACCACAGCG
RT-dmt-F GCCTTTCATTCCTGCCGAGTTCA Amplification of a 161-bp fragment of dmt by RT-qPCR
RT-dmt-R TGGAGAAGGTGGACGGCGACAGATA
RT-metF-F GTCCGCATCCGTGCTGAGCAAATAT Amplification of a 138-bp fragment of metF by RT-qPCR
RT-metF-R AAAGGGTAGAAGTGCAGGCGGACAT
RT-purU-F TTGACCATTGCCTGGGTGACCTGCT Amplification of a 128-bp fragment of purU by RT-qPCR
RT-purU-R GAACGGGACGCCACGGAGCGATGAG
RT-dhc-F CATAAAGCCTGCGAAGGACGTGGA Amplification of a 167-bp fragment of dhc by RT-qPCR
RT-dhc-R TCGACTTTCCGATCACCACAGCG
RT-16S-F GGCGACGATCCATAGCTGGTCTGAG Amplification of a 141-bp fragment of 16S rRNA by RT-qPCR
RT-16S-R TTCATCACTCACGCGGCATTGCTG
a

Restriction sites are underlined.