Difference between revisions of "Team:Tongji China/Light control"

We use the light-off system from 2017 SSTi-SZGD to kill our bacteria after effecting.
It contains two parts.



One is a light-repressed system containing a single light repressor LexA-VVD, and a ColE promoter containing an SOS operator sequence for LexA binding, regulates the expression of target genes.

Upon light exposure, the light-switchable repressor LEVI[1] is induced to form homodimers, which then bind to the operator sequence and repress the activity of a promoter by blocking the attachment of RNA polymerase to the promoter. Removal of blue light results in gradual dissociation of the dimers and transcription activation. I repressor, which can repress the activity of the R-O12 promoter, is under the control of the LightOff system. Upon light illumination, LEVI homodimerizes, then represses the expression of cI repressor and initiates target gene expression.



Another is for the target gene to kill the bacteria, there we use a suicide gene that encodes Supernova[2], which is a mutant form of well-known KillerRed, the first engineered genetically-encoded photosensitizer. Photosensitizer contains chromophores that generate reactive oxygen species (ROS) upon illumination, and it is commonly used for illumination-induced destruction of targeted cells.

In general, it forms a light switch and a killer to control the lives of our bacteria, it confirms the safety of our whole project.
After our bacteria are released in the gut environment for several hours, they can be eliminated by our immune system. Our project uses this method to ensure the bacteria to be dead the time they are released into the environment. It can be safe for humans and friendly to the environment.

Then we conduct some experiments to verify the kill-switch's function.
However, the amount of the P. aeruginosa does not show significant reduction after the lighting. We indicate that the plasmid electrotransformation may be not quite successful. Or may because the type of bacteria--Pseudomonas aeruginosa has not been used in this method before, and the plasmid vitality in the bacteria is lower than in Escherichia coli. We are searching for other reasons, like the promotor strength, codon degeneracy and so on. We will solve the problem in the future.