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	<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>		<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>
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	<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>
-	<center><u>Figure 1: Delivery by bacteria engineered</u></center>	+	<center><u>Figure 1: Enginereed bacteria delivery to tadpole</u></center>
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	<p>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: <br>		<p>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: <br>

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Revision as of 20:11, 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.

Figure 1: Enginereed bacteria delivery to tadpole

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:

Figure 2: Fluorescence quantification The results show that, except for the control, all tadpoles are fluorescent. The Fig.2 shows also that the fluorescence occurs mainly in the intestinal tract. The death rate during for the experiments is close to 0%. We've performed the same using the Imperial College 2011 plasmid; the tadpoles didn't show any sign of auxin intolerance.