Team:Evry/BXcom
From 2012.igem.org
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<h2>Steps</h2> | <h2>Steps</h2> | ||
- | <p>Our idea was to use previous biobricks from Imperial College 2011 <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K515100">BBa_K515100</a>. Indeed, they managed to express in <i>Escherichia coli</i> the genes encoding the IAA-producing pathway from <i>Pseudomonas savastanoi</i>. Besides, we constructed a plasmid with a reporter (mRFP) as a control to | + | <p>Our idea was to use previous biobricks from Imperial College 2011 <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K515100">BBa_K515100</a>. Indeed, they managed to express in <i>Escherichia coli</i> the genes encoding the IAA-producing pathway from <i>Pseudomonas savastanoi</i>. Besides, we constructed a plasmid with a reporter (mRFP) as a control to monitor the auxin production.</p> |
<center><img src="https://static.igem.org/mediawiki/2012/e/eb/Fig1.png"/></center><br> | <center><img src="https://static.igem.org/mediawiki/2012/e/eb/Fig1.png"/></center><br> |
Revision as of 20:09, 25 September 2012
Communication Bacteria<->Xenopus
Overview
Engineering the tadpole with AID system raised a question how will we deliver auxin to the embryo? One of the ideas was to use bacteria as a delivery machine in order to create a communication between two engineered organisms.
Steps
Our idea was to use previous biobricks from Imperial College 2011 BBa_K515100. Indeed, they managed to express in Escherichia coli the genes encoding the IAA-producing pathway from Pseudomonas savastanoi. Besides, we constructed a plasmid with a reporter (mRFP) as a control to monitor the auxin production.
Once all the construction prepared/analyzed in DH5a bacteria, we prepared a mix with bacteria and MMR medium and LB medium. So in a 16-well plates, wich each contains three tadpoles we proceedeed as: