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. 2017 Apr 4;7:45936. doi: 10.1038/srep45936

Figure 1. The mapping of the inserted DNA fragment in the recombinant plasmid pUC-DP61 and subcloning strategy of the gene upf0118.

Figure 1

One C-terminus truncated ORF and three intact ORFs are included in a 4.4-kb DNA fragment inserted into the recombinant plasmid pUC-DP61, each of which is preceded by a respective promoter-like sequence and a respective Shine-Dalgarno (SD) sequence. A predicted promoter sequence (−35 region and −10 region) and Shine-Dalgarno (SD) sequence, the initiation codon TTG of ORF3 designated UPF0118 (Genbank accession No. KY231907), the enzymatic site of SalI and EcoRI are underlined. The stop codon TAA of ORF3 is indicated by the asterisk and a possible terminator following ORF3 indicated by inverted solid arrows. UPF0118 was subcloned, together with its promoter-like and SD sequences, into SalI- and EcoRI-digested pUC18 through digestion by the same two restriction enzymes and ligation.