Team:ETH Zurich/lab/biobrick/used1

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<partinfo>BBa_R0062 AddReview 4</partinfo> ETH Zurich 2014

Contents

Characterization of the promoter's basal leakiness to LuxR in the absence of 3OC6-HSL

The amount of regulator LuxR (BBa_C0062) in the system was shown to influence the pLuxR promoter's basal expression or leakiness. By using the three different constitutive promoters BBa_J23100, BBa_J23109, and BBa_J23111 for the production of LuxR we could measure this effect in terms of fluorescence.

Background information

We used an E. coli TOP10 strain

Systems considered

Modeling leakiness

Results

Characterization of the promoter's sensitivity to 3OC6-HSL depending on LuxR concentration

Background information

Systems considered

Modeling promoter's sensitivity

Results

Characterization of two-level crosstalk on the promoter

Background information

System considered

Modeling crosstalk

First-order crosstalk

First Level crosstalk: LuxR binds to different HSL and activates the promoter

ETH Zurich 1crosstalkPlux.png

Second Level crosstalk: other regulatory proteins, like LasR, bind to their natural HSL substrate and activates the promoter

ETH Zurich 2crosstalkPlux.png

Second order crosstalk: Combination of both cross-talk levels

Other regulatory proteins, like LasR, bind to different HSL and activates the promoter

ETH Zurich 3crosstalkPlux.png

Results

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