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. 2022 Aug 11;13:978577. doi: 10.3389/fmicb.2022.978577

Table 2.

Primers used in this study.

Primer DNA sequence (5′–3′)a Purpose
27F 5´-AGAGTTTGATCCTGGCTCAG-3´ Amplification of the 16S rRNA gene of the dicamba degrader
1492R 5´-GGTTACCTTGTTACGACTT-3´
pET-dmt06-F TAAGAAGGAGATATACATATGGGAGAAGGACGGTCCCTTCA Amplification of dmt06 gene for expression in E. coli BL21
pET-dmt06-R AGTGCGGCCGCAAGCTTCGGCGACCCGGCGGCCGTCGCC
dF1 CTC(G)TTCG(A)ACCAGT(A)CC(G)CACCACATG Amplification of the conserved regions of dmt06 gene
dF2 TCGGCGACT(G)GC(G)ATCCTG(T)TAC(T)TA(G)
dR1 GGC(A)TGGATC(G)C(G)CC(G)TACCCG(C)CTG(C)GCCG
dR2 TC(G)AAGTTC(T)GAC(T)CAC(T)GACTTCATCGG
uSP1 AGTACACGATGCAGTCGCCGACCACGT Amplification of the upstream sequence of dmt06
uSP2
uSP3
AACCCGGCGAAGGTGTTGATGCCGA
CTTTCAGGAACAGCTNNNNNNNNNGGTGGG
dSP1 AGTGGAGCTGTCCGGCCCGTAC Amplification of the downstream sequence of dmt06
dSP2 GACACCGTACGGTCGGCCATTCTC
dSP3 AGAAGTACGGAATCGNNNNNNNNNGCACCC
a

The underlined bases indicate that they were overlapped and were used to construct plasmids by the In-Fusion.