Team:Uppsala University/Promoters

This bar diagram shows the differences measured fluorescence between different promoters in each strand, data from one lab strain should not be compared to the other lab strain since these haven't been grown under exactly same conditions.

Since we didn't know a promoter strength which would fit for the screening systems to give a working artificial small RNA/ 5´UTR-SYFP mRNA ratio we had to assemble with promoters of various strengths, for this we chose J23106, J23110 and PlacIQ.

To prevent future unnecessary assembling by our or any other team we conducted a promoter test of the promoters used in in this years iGEM project. Also interested in the strengths of the commonly used promoters Plac and PlacIQ.

The promoter test was conducted by measuring fluorescence expressed by each individual promoter assembled with B0032-SYFP2 (BBa_K864101) though a FACS (fluorescence activated cell sorter) in lab strains MG1655 and DH5α.

The test was conducted on triplicated cultures of each promoter construct, which were measured in the FACS. For each culture 10⁵ cells fluorescence were measured individually, dead cells and non fluorescent cells were discarded, and a average where calculated. All promoter constructs of each strain were grown under same conditions.

The variance in expression between MG1655 and DH5α may depend on the J23101-B0032-SYFP2, which is the promoter the other promoters strength is calculated from, construct in DH5α might been a weaker phenotype resulting in higher RPU values to other DH5α. Alternatively the maximum protein expression is lower in DH5α due to its lower fitness also resulting in lower expression of SYFP2 in the J23101 construct.