Team:Cambridge

From 2009.igem.org

(Difference between revisions)
(E. Chromi)
(E. Chromi)
Line 7: Line 7:
Previous iGEM teams have focused on genetically engineering bacterial biosensors by enabling bacteria to respond to novel inputs, especially biologically significant compounds. There is an unmistakable need to also develop devices that can 1) manipulate input by changing the behaviour of the response of the input-sensitive promoter, and that can 2) report a response using clear, user-friendly outputs. The most popular output is the expression of a fluorescent protein, detectable using fluorescence microscopy. But, what if we could simply see the output with our own eyes?  
Previous iGEM teams have focused on genetically engineering bacterial biosensors by enabling bacteria to respond to novel inputs, especially biologically significant compounds. There is an unmistakable need to also develop devices that can 1) manipulate input by changing the behaviour of the response of the input-sensitive promoter, and that can 2) report a response using clear, user-friendly outputs. The most popular output is the expression of a fluorescent protein, detectable using fluorescence microscopy. But, what if we could simply see the output with our own eyes?  
-
We successfully characterised a set of transcriptional systems for calibrated output - Sensitivity Tuners.  We also successfully expressed a spectrum of pigments in ''E. coli,'' designing a set of Colour Generators.
+
We successfully characterised a set of transcriptional systems for calibrated output - [[https://2009.igem.org/Team:Cambridge/Project/Amplification |Sensitivity Tuners]].  We also successfully expressed a spectrum of pigments in ''E. coli,'' designing a set of [[https://2009.igem.org/Team:Cambridge/Project/Pigments | Colour Generators]]

Revision as of 22:17, 21 October 2009


E. Chromi

Cambridge Frontpage2.png

The Cambridge 2009 iGEM team has created two kits of parts that will facilitate the design and construction of biosensors in the the future.

Previous iGEM teams have focused on genetically engineering bacterial biosensors by enabling bacteria to respond to novel inputs, especially biologically significant compounds. There is an unmistakable need to also develop devices that can 1) manipulate input by changing the behaviour of the response of the input-sensitive promoter, and that can 2) report a response using clear, user-friendly outputs. The most popular output is the expression of a fluorescent protein, detectable using fluorescence microscopy. But, what if we could simply see the output with our own eyes?

We successfully characterised a set of transcriptional systems for calibrated output - [|Sensitivity Tuners]. We also successfully expressed a spectrum of pigments in E. coli, designing a set of [| Colour Generators]















Cambridge Sponsor Logo1.pngCambridge Sponsor Logo2.pngCambridge Sponsor Logo3.pngCambridge Sponsor Logo4.pngCambridge Sponsor Logo5.pngCambridge Sponsor Logo8.pngCambridge Sponsor Logo6.pngCambridge Sponsor Logo7.pngCambridge Sponsor Logo9.pngCambridge Sponsor Logo10.pngCambridge Sponsor Logo11.pngCambridge Sponsor Logo12.pngCambridge Sponsor Logo14.pngCambridge Sponsor Logo13.pngCambridge Sponsor Logo15.pngCambridge Sponsor Logo16.pngCambridge Sponsor Logo17.pngCambridge Sponsor Logo18.pngCambridge Sponsor Logo19.pngBmglab.jpg