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. 2020 Jan 29;202(4):e00700-19. doi: 10.1128/JB.00700-19

TABLE 3.

Plasmids used in this study

Plasmid Description Reference or source
pMQ30 7.5-kb mobilizable vector; oriT sacB Gmr 57
pLD2722 Gmr Tetr; flanked by Flp recombinase target (FRT) sites to resolve out resistance cassettes 7
pFLP2 Flp recombinase-producing plasmid 62
pLD1929 Δcco1 cco2 PCR fragment introduced into pMQ30 by gap repair cloning in yeast strain InvSc1 7
pLD1966 Δcox (aa3) PCR fragment introduced into pMQ30 by gap repair cloning in yeast strain InvSc1 This study
pLD1967 Δcyo (bo3) PCR fragment introduced into pMQ30 by gap repair cloning in yeast strain InvSc1 This study
pLD2044 Δcio PCR fragment introduced into pMQ30 by gap repair cloning in yeast strain InvSc1 This study
pLD2958 PCR-amplified cox (aa3) promoter ligated into pLD2722 using SpeI and XhoI This study
pLD2960 PCR-amplified cio promoter ligated into pLD2722 using SpeI and XhoI This study
pLD2777 PCR-amplified cco1 promoter ligated into pLD2722 using SpeI and XhoI 7
pLD2778 PCR-amplified cco2 promoter ligated into pLD2722 using SpeI and XhoI 7