Team:EPF Lausanne/Sensing-Effector

From 2013.igem.org

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The Idea of this module was to transform the bacterium with a plasmid that would contain a promoter which senses a specific signal. Once this promoter senses the signal, it would initiate transcribtion of an enzyme which degrades the nanocapsule, thus releasing its contents.
The Idea of this module was to transform the bacterium with a plasmid that would contain a promoter which senses a specific signal. Once this promoter senses the signal, it would initiate transcribtion of an enzyme which degrades the nanocapsule, thus releasing its contents.
We decided to use pH as the specific trigger that activates the promoter. As a proof of principle, we inserted three different promoters into three plasmid in front of the bio brick BBa_I746916 which encodes superfolded GFP. Then we transformed cells with these plasmids and let them grow in media with different pHs in order to check the expression.
We decided to use pH as the specific trigger that activates the promoter. As a proof of principle, we inserted three different promoters into three plasmid in front of the bio brick BBa_I746916 which encodes superfolded GFP. Then we transformed cells with these plasmids and let them grow in media with different pHs in order to check the expression.
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Experiments
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We chose the following three pH sensitive promoters:
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1.) Hya-promoter, isolated from the Escherichia Coli K-12 MG1655 strain
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2.) Cad-promoter, isolated from the Escherichia Coli K-12 MG1655 strain
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3.) BioBrick BBa_J23119, a constitutive promoter that was make by the 2006 Berkley team.
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All the promoters were isolated by PCR and then assembled into the pSB1C3 Plasmid in front of the superfolded GFP.
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Revision as of 08:22, 29 September 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Sensing

Overview

The Idea of this module was to transform the bacterium with a plasmid that would contain a promoter which senses a specific signal. Once this promoter senses the signal, it would initiate transcribtion of an enzyme which degrades the nanocapsule, thus releasing its contents. We decided to use pH as the specific trigger that activates the promoter. As a proof of principle, we inserted three different promoters into three plasmid in front of the bio brick BBa_I746916 which encodes superfolded GFP. Then we transformed cells with these plasmids and let them grow in media with different pHs in order to check the expression.

Experiments

We chose the following three pH sensitive promoters: 1.) Hya-promoter, isolated from the Escherichia Coli K-12 MG1655 strain 2.) Cad-promoter, isolated from the Escherichia Coli K-12 MG1655 strain 3.) BioBrick BBa_J23119, a constitutive promoter that was make by the 2006 Berkley team.

All the promoters were isolated by PCR and then assembled into the pSB1C3 Plasmid in front of the superfolded GFP.

Wiki Links

Retrieved from "http://2013.igem.org/Team:EPF_Lausanne/Sensing-Effector"