Skip to main content
. 2019 Mar 6;10:457. doi: 10.3389/fmicb.2019.00457

FIGURE 5.

FIGURE 5

Identification of promoter regions driving expression of mpsA and mpsB. The fragments cloned into the complementing plasmids are shown below the schematic map of mobSGI1 region. Putative promoter elements predicted by BPROM or found by manual search are indicated by blue or yellow arrowheads, respectively. Other symbols are as in Figure 1B. Transfer frequency of SGI1-CΔS020 and SGI1-CΔS019 was measured in the presence of one of the complementing plasmids and the helper plasmid R55ΔTn6187. Plasmid pMSZ984 showed high st. deviations in three independent complementation assays carried out with 3–6 replicates with SGI1-CΔS019, thus the complementation efficiency of this plasmid could not exactly be determined. However, mean values appeared similar to that of pMSZ981 and pMSZ996. Transconjugants resulting from oriTSGI1-independent transfer pathway.