Team:Paris Bettencourt/Experiments/T7 diffusion
From 2011.igem.org
Line 51: | Line 51: | ||
|- | |- | ||
|[[File:T7 loop 2.jpg|290px|thumb|center|E-Coli at 37°C (trans image)]] | |[[File:T7 loop 2.jpg|290px|thumb|center|E-Coli at 37°C (trans image)]] | ||
- | |[[File:T7 loop | + | |[[File:T7 loop 2 gfp.jpg|290px|thumb|center|E-Coli at 37°C (gfp image)]] |
|[[File:T7 loop 2 rfp.jpg|290px|thumb|center|-Coli at 37°C (rfp image)]] | |[[File:T7 loop 2 rfp.jpg|290px|thumb|center|-Coli at 37°C (rfp image)]] | ||
|} | |} |
Revision as of 13:18, 21 September 2011
Characterization of the T7 signal amplification leakage in E. Coli
We characterized T7 autoloop in E. Coli, when hosted in the plasmid pSB1C3 (the K606036 part). The idea was to see if the system was leaky inside a synthetic biology plasmid, that is to say, a plasmid holding 4 terminators before any construct.
We found out that there is a leakage, but it is small. The cells in which the positive feed back look is activated stop deviding and glow with a very strong signal. Here are the images commented
The first pictures show that RFP construct has been well done. Indeed, we can see that some cells are glowing with RFP fluorescence. This also shows that the system is a bit leaky. Moreover the autoloop system is working very well because when leak occurs, cells glow highly.
This pictures show that GFP system gives more disparity than the RFP construct. This is probably due to the LB that already glows in green. It is also noticeable that B.Subtilis is naturally shining green.