University of Texas 2006

From 2006.igem.org

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
 +
==Members==
 +
The UT Austin team is:
The UT Austin team is:
* Aaron Chevalier
* Aaron Chevalier
Line 13: Line 15:
==Edge Detector==
==Edge Detector==
-
For the 2004 Synthetic Biology Competition, our joint UT-Austin/UCSF team designed a genetically encoded edge detection device.  In our system, a lawn of genetically identical precursor ''E.coli'' would be subjected to a light image, and only those cells at the light/dark boundary would become active and express a genetic reporter.
+
For the 2004 Synthetic Biology Competition, our joint UT-Austin/UCSF team designed a genetically encoded edge detection device.  In our system, a community of genetically identical ''E.coli'' would function as a massively parallel computer capable of calculating the light/dark boundary of an arbitrary two-dimensional image.
-
An obvious hurdle in the implementation of this system was genetically encoding light detection in an easily manipulate-able and tractable system like ''E.coli''.  To accomplish this, we used an incredible part engineered in the Voigt lab.  This part, Cph8, ([http://parts2.mit.edu/r/parts/partsdb/view.cgi?part_id=5302 I15010]) is an engineered fusion between a cyanobacterial light sensing phytochrome (Cph1) and an ''E.coli'' transmembrane histidine kinase, (EnvZ).  660nm light causes an isomerization in the Cph1 domain of the chimera which strongly inactivates the histidine kinase acitity of EnvZ.  When EnvZ is inhibited, a phosphorelay cascade which activates transcription from the ''OmpC'' promoter [http://parts2.mit.edu/r/parts/partsdb/view.cgi?part_id=3910 R0082]) and inhibits transcription from the ''OmpF'' promoter ([http://parts2.mit.edu/r/parts/partsdb/view.cgi?part_id=3915 R0084]).  We showed that when this system is expressed in ''E.coli'', it is possible to transform each cell on an agar surface into a decision making pixel capable of deciding whether it is in the light or dark.  The community of cells is therefore capable of genetically reproducing a light image (figure to come).
+
An obvious hurdle in the implementation of this system was genetically encoding light detection in an easily manipulate-able and tractable system like ''E.coli''.  To accomplish this, we used a synthetic part engineered in the Voigt lab.  This part, Cph8, ([http://parts2.mit.edu/r/parts/partsdb/view.cgi?part_id=5302 I15010]) is an engineered fusion between a cyanobacterial light sensing phytochrome (Cph1) and an ''E.coli'' transmembrane histidine kinase, (EnvZ).  660nm light causes an isomerization in the Cph1 domain of the chimera which inactivates the histidine kinase acitity of EnvZ.  When EnvZ is inhibited, a phosphorelay cascade which activates transcription from the ''OmpC'' promoter [http://parts2.mit.edu/r/parts/partsdb/view.cgi?part_id=3910 R0082]) and inhibits transcription from the ''OmpF'' promoter ([http://parts2.mit.edu/r/parts/partsdb/view.cgi?part_id=3915 R0084]).  We showed that when this system is expressed in ''E.coli'', it is possible to transform each cell on an agar surface into a decision making pixel capable of deciding whether it is in the light or dark.  The community of cells is therefore capable of genetically reproducing a light image.
This was the first step in engineering the edge detector, a massively parallel computation system that should be able to easily compute the edge of a complex light image; a very hard serial computation problem.  We have now built the entire edge detection circuit ([http://partsregistry.org/Part:BBa_I15022 I15022]).
This was the first step in engineering the edge detector, a massively parallel computation system that should be able to easily compute the edge of a complex light image; a very hard serial computation problem.  We have now built the entire edge detection circuit ([http://partsregistry.org/Part:BBa_I15022 I15022]).

Revision as of 01:16, 1 November 2006

Members

The UT Austin team is:

Advisors:

Edge Detector

For the 2004 Synthetic Biology Competition, our joint UT-Austin/UCSF team designed a genetically encoded edge detection device. In our system, a community of genetically identical E.coli would function as a massively parallel computer capable of calculating the light/dark boundary of an arbitrary two-dimensional image.

An obvious hurdle in the implementation of this system was genetically encoding light detection in an easily manipulate-able and tractable system like E.coli. To accomplish this, we used a synthetic part engineered in the Voigt lab. This part, Cph8, (I15010) is an engineered fusion between a cyanobacterial light sensing phytochrome (Cph1) and an E.coli transmembrane histidine kinase, (EnvZ). 660nm light causes an isomerization in the Cph1 domain of the chimera which inactivates the histidine kinase acitity of EnvZ. When EnvZ is inhibited, a phosphorelay cascade which activates transcription from the OmpC promoter R0082) and inhibits transcription from the OmpF promoter (R0084). We showed that when this system is expressed in E.coli, it is possible to transform each cell on an agar surface into a decision making pixel capable of deciding whether it is in the light or dark. The community of cells is therefore capable of genetically reproducing a light image.

This was the first step in engineering the edge detector, a massively parallel computation system that should be able to easily compute the edge of a complex light image; a very hard serial computation problem. We have now built the entire edge detection circuit (I15022).


Edge Detector Circuit. Light represses the expression of 2 genes; a biosynthetic gene for a membrane diffusible quorum sensing activator, and a dominant transcriptional repressor.


















A light image is projected onto an agar plate of genetically identical E.coli. Cells residing in dark areas are repressed by CI repressor, but produce a diffusible inducer, AHL. Cells in illuminated areas do not express CI repressor, and are therefore sensitive to AHL. If they neighbor a dark area, they will be activated by locally diffusing AHL. In this way, only cells at the light dark boundary express a reporter.
Personal tools
Past/present/future years