Team:ETH Zurich/Templates/Test

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<h1>Final Circuit</h1>
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      <a href="/Team:ETH_Zurich/Team"><img src="/wiki/images/f/f7/Team_picture.JPG" /></a>
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      <p style="font-size:16px" align="justify"><b>Team</b><br>We are a team of seven highly motivated Bachelor- and Master Students at the ETH Zurich pursuing various fields such as Biotechnology,  Biomedical Engineering, Neurobiology and Bioinformatics. The iGEM project is carried out at one of the youngest departments of ETHZ located in Basel-Department of Biosystems Science and Engineering - flourishing in interdisciplinary biological research. If you're around Basel, make sure to visit our team's lab to play the bio-game Colisweeper!</p>
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      <a href="/Team:ETH_Zurich/Project"><img src="https://static.igem.org/mediawiki/2013/8/8f/Minetocoli3.png"/></a>
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      <p style="font-size:15px" align="justify"><b>From Minesweeper to Colisweeper</b><br> Our project-Colisweeper- is a biological version of the computer game Minesweeper. The minefield is replaced by mine and non-mine colonies on an agar plate. Quorum sensing molecule OHHL communicates between colonies which are designed to express different orthogonal hydrolases depending on the signal processed. By pipetting a colorless multi-substrate mix onto mine or non-mine colonies, color appears which indicates the next logical move for the player. If you are certain of a mine colony, you can use a second substrate solution to flag the mine.
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<p>For the final Colisweeper circuit we plan a four plasmid system. The mine cells constitutively express LuxI for signal generation and NagZ as identifier hydrolase. In the non-mine cells LuxR is expressed constitutively to process the OHHL signal. PhoA is expressed constitutively as well as reporter for safe cells. Aes and GusA are expressed from pLux promoters with different sensitivities. You can find all the biobricks we used and our own new biobricks in the figure below.</p>
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    <p style="font-size:15px" align="justify"><b>Information Processing</b><br> Our non-mine colonies are designed to distinguish between different concentrations of OHHL that translate this information into expression of different sets of hydrolases. They are equipped with mutated LuxR promoters with different OHHL sensitivities which serve as highpass filters. The promoters were created using site-saturation mutagenesis. Through mutation of the LuxR binding sites we were able to tune the promoters to different OHHL affinities .</p>
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      <a href="https://2013.igem.org/Team:ETH_Zurich/Experiments_3"><img src="https://static.igem.org/mediawiki/2013/5/54/2013-09-16_09.30_%281%29.png"/></a>   
 
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      <p style="font-size:15px" align="justify"><b>Hydrolase Reactions</b><br> We use a set of orthogonal hydrolases as our reporter system that react within minutes with the added multi-substrate to produce a visible color. The set of hydrolases such as alkaline phosphatase (<i>phoA</i>), β-galactosidase (<i>lacZ</i>), acetylesterase (<i>aes</i>), β-N-Acetylglucosaminidase (<i>nagZ</i>) and β-glucuronidase (<i>gusA</i>) and their respective substrates react to achieve fast and colorful outputs with each color indicative of the next logical move for the player.</p>
 
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      <a href="/Team:ETH_Zurich/GFP"><img src="https://static.igem.org/mediawiki/2013/6/63/Modeldiffusion.png"/></a>   
 
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      <p style="font-size:15px"><b>The Model</b><br> As our system is based on quorum sensing of OHHL, the diffusion of OHHL in the mine field is a vital part of the system. We study the diffusion in our system in a hexagonal grid format with mine and non-mine colonies using a spatio-temporal model. The information from the model was used to validate and improve our system.
 
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      <p style="font-size:15px" align="justify"><b>Experiments</b><br>Starting with characterization of the OHHL diffusion in agar plates we went on to test different sender- and receiver-cell pairs in the hexagonal grid. Initially we used Green fluorescent Protein (GFP) as a reporter to study the OHHL interaction between mine and non mine colonies. Together with promoter mutagenesis and screening, we also tested and characterized different hydrolase-substrate pairs which are crucial to get the game going!</p>
 
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<img src="https://static.igem.org/mediawiki/2013/thumb/b/b7/Plasmidmap.png/800px-Plasmidmap.png" usemap="#map3" id="imagemap3" >
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<map id="map3" name="map3"> <area shape="rect" alt="" title="NagZ: BBa_K1216003" coords="259,77,340,114" href="http://parts.igem.org/Part:BBa_K1216003" target="" /><area shape="poly" alt="" title="constitutive promoter: BBa_J23100" coords="161,86,215,82,215,70,244,98,216,123,216,109,158,108" href="http://parts.igem.org/Part:BBa_J23100" target="" /><area shape="rect" alt="" title="LuxI: BBa_K805016" coords="255,230,327,263" href="http://parts.igem.org/Part:BBa_K805016" target="" /><area shape="poly" alt="" title="constitutive promoter: BBa_J23110" coords="157,245,211,240,210,231,239,258,216,277,217,266,152,266" href="http://parts.igem.org/Part:BBa_J23110" target="" /><area shape="rect" alt="" title="" coords="682,76,763,113" href="" target="" /><area shape="poly" alt="" title="" coords="591,105,652,95,648,81,676,104,654,132,651,116,594,125" href="" target="" /><area shape="poly" alt="" title="" coords="782,85,841,88,843,74,863,102,839,124,839,110,780,107" href="" target="" /><area shape="poly" alt="" title="" coords="881,85,965,99,960,131,875,119" href="" target="" /><area shape="poly" alt="" title="" coords="581,263,642,254,637,238,664,264,643,292,640,275,581,287" href="" target="" /><area shape="rect" alt="" title="" coords="675,237,738,272" href="" target="" /><area shape="rect" alt="" title="" coords="872,244,951,277" href="" target="" /><area shape="poly" alt="" title="" coords="768,246,828,247,827,230,853,257,828,280,828,267,767,270" href="" target="" />
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      <p style="font-size:15px" align="justify"><b>Human practices</b><br>As an inspiration from our project, we analyzed the relationship between synthetic biology and games. For one thing synthetic biology can be used to play common games in a new way, possibly for educational purposes or as a basis for proof-of-principle experiments for new circuits. More recently synthetic biologists also started to use games as a research tool, an innovative approach to make use of crowd-sourcing and distributed computing. We want to find correlations and discuss possible consequences for Synthetic Biology.</p>
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<p align="justify">Colisweeper is an interactive, biological version of the Minesweeper computer game, based on luxI/luxR quorum sensing and chromogenic enzymatic reactions. The goal is to clear an agar “minefield” without detonating mines.<br>Genetically engineered <i>Escherichia coli</i> colonies are used as sender-cells (mines) and receiver-cells (non-mines). Mines secrete the signaling molecule N-(3-oxohexanoyl)-l-homoserine lactone (OHHL) whereas non-mines process the signal. To distinguish between OHHL-levels, a library of PLuxR promoters with various sensitivities was created through site-saturation mutagenesis. High-pass filters were constructed to control the expression of different orthogonal hydrolases in non-mines, depending on the number of surrounding mines. <br>Additionally, the mines express their own hydrolase.A spatiotemporal reaction-diffusion model was established to evaluate and improve the system. To play Colisweeper, a colorless substrate solution is pipetted onto a colony of choice. The result is a defined color change within minutes, allowing identification of the played colony and the number of mines surrounding it.  
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<br><h1>Cloned Constructs</h1>
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<p>To get to the circuit mentioned above we tested different versions of the circuit. For example we started our experiments using GFP as a reporter instead of the hydrolases. Then we also tested different LuxI and LuxR generating constructs. In the following table we list all the biobricks we used, the plasmids we cloned and what experiments we used them for. In general we used standard biobrick cloning techniques as described in the methods section. Whenever we used PCR gene amplification for cloning, we list the primers used in the following table. To be able to co-transform different plasmids we used backbones with compatible origins of replication and resistance genes. In the table you can find which backbone versions we used for which constructs.</p>
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<table style="float:left;margin-top:10px;width:auto;height:auto;font-size:12px">
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<th colspan="4" height="30px">GFP constructs</th>
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<th width="20px" height="30px">  </th>
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<th width="475px" height="30px">Description</th>
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<th width="475px" height="30px">Cloning</th>
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<th width="350px" height="30px">Maps</th>
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<td>1</td>
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<td>Receiver cell construct for GFP diffusion experiments</td>
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<td>[http://parts.igem.org/Part:BBa_J09855 BBa_J09855] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_E0840 BBa_E0840] insert (XbaI, PstI)</td>
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<td>[[File:Map1.png|300px]]</td>
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<td>2</td>
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<td>Library of the Receiver cell constructs</td>
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<td>Using the BBa_J09855-E0840 construct a library with mutated pLux promoters was created through site-saturation mutagenesis to screen for promoters with changed sensitivities for OHHL:</td>
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<td>[[File:Map2.png|300px]]</td>
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<td>3</td>
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<td>Receiver cell construct for GFP experiments without the LuxR generating part</td>
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<td>[http://parts.igem.org/Part:BBa_R0062 BBa_R0062] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_E0840 BBa_E0840] insert (XbaI, PstI)</td>
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<td>[[File:Map3a.png|225px]]<br>[[File:Map3b.png|225px]]</td>
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<table style="float:left;margin-top:10px;width:auto;height:auto;font-size:12px">
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<th colspan="4" height="30px">LuxI generating constructs</th>
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<th width="20px" height="30px">  </th>
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<th width="475px" height="30px">Description</th>
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<th width="475px" height="30px">Cloning</th>
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<th width="350px" height="30px">Maps</th>
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<td>4</td>
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<td>Sender cell construct with a very strong constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments</td>
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<td>[http://parts.igem.org/Part:BBa_J23100 BBa_J23100] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)</td>
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<td>[[File:Map4b.png|225px]]<br>[[File:Map4a.png|225px]]</td>
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<td>5</td>
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<td>Sender cell construct with an intermediate constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments</td>
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<td>[http://parts.igem.org/Part:BBa_J23118 BBa_J23118] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)</td>
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<td>[[File:Map4b.png|225px]]<br>[[File:Map4a.png|225px]]<br>[[File:Map5c.png|225px]]</td>
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<td>6</td>
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<td>Sender cell construct with an intermediate constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments</td>
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<td>[http://parts.igem.org/Part:BBa_J23110 BBa_J23110] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)</td>
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<td>[[File:Map4b.png|225px]]<br>[[File:Map4a.png|225px]]<br>[[File:Map5c.png|225px]]</td>
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<td>7</td>
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<td>Sender cell construct with a weak constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments</td>
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<td>[http://parts.igem.org/Part:BBa_J23114 BBa_J23114] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)</td>
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<td>[[File:Map4b.png|225px]]<br>[[File:Map4a.png|225px]]</td>
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<th colspan="4" height="30px">LuxR generating constructs</th>
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<th width="20px" height="30px">  </th>
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<th width="475px" height="30px">Description</th>
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<th width="475px" height="30px">Cloning</th>
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<th width="350px" height="30px">Maps</th>
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<td>8</td>
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<td>constitutive LuxR generating biobrick</td>
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<td>[http://parts.igem.org/Part:BBa_J09855 BBa_J09855]</td>
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<td>[[File:Map8.png|250px]]</td>
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<td>9</td>
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<td>constitutive LuxR generating biobrick, with negative feedback-loop at high OHHL concentrations</td>
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<td>[http://parts.igem.org/Part:BBa_F2621 BBa_F2621]</td>
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<td>[[File:Map9.png|250px]]</td>
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<td>10</td>
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<td>constitutive LuxR generating construct, repressible through LacI</td>
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<td>[http://parts.igem.org/Part:BBa_R0010 BBa_R0010] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_I0462 BBa_I0462] insert (XbaI, PstI)</td>
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<td>[[File:Map10.png|225px]]</td>
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<td>11</td>
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<td>constitutive LuxR generating construct, with negative feedback-loop at high OHHL concentrations</td>
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<td>[http://parts.igem.org/Part:BBa_R0063 BBa_R0063] backbone (SpeI,PstI) and [http://parts.igem.org/Part:BBa_I0462 BBa_I0462] insert (XbaI, PstI)</td>
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<td>[[File:Map11.png|225px]]</td>
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<td>12</td>
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<td>auto-inducible LuxR generating construct with positive feedback loop</td>
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<td>[http://parts.igem.org/Part:BBa_R0062 BBa_R0062] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_I0462 BBa_I0462] insert (XbaI, PstI)</td>
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<td>[[File:Map12.png|225px]]</td>
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</tr>
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<td>13</td>
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<td>negatively regulated pLuxL-LacI construct to improve leakiness of LuxR system</td>
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<td>[http://parts.igem.org/Part:BBa_R0063 BBa_R0063] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_C0012 BBa_C0012] insert (SpeI,PstI)</td>
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<td>[[File:Map13.png|225px]]</td>
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<th width="20px" height="30px">  </th>
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<th width="475px" height="30px">Description</th>
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<th width="475px" height="30px">Cloning</th>
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<th width="350px" height="30px">Maps</th>
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<th width="20px" height="30px">  </th>
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<th width="475px" height="30px">Description</th>
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<th width="475px" height="30px">Cloning</th>
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<th width="350px" height="30px">Maps</th>
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Latest revision as of 06:22, 24 September 2013

Header2.png
80px-Eth igem logo.png

Final Circuit

For the final Colisweeper circuit we plan a four plasmid system. The mine cells constitutively express LuxI for signal generation and NagZ as identifier hydrolase. In the non-mine cells LuxR is expressed constitutively to process the OHHL signal. PhoA is expressed constitutively as well as reporter for safe cells. Aes and GusA are expressed from pLux promoters with different sensitivities. You can find all the biobricks we used and our own new biobricks in the figure below.



Cloned Constructs

To get to the circuit mentioned above we tested different versions of the circuit. For example we started our experiments using GFP as a reporter instead of the hydrolases. Then we also tested different LuxI and LuxR generating constructs. In the following table we list all the biobricks we used, the plasmids we cloned and what experiments we used them for. In general we used standard biobrick cloning techniques as described in the methods section. Whenever we used PCR gene amplification for cloning, we list the primers used in the following table. To be able to co-transform different plasmids we used backbones with compatible origins of replication and resistance genes. In the table you can find which backbone versions we used for which constructs.

GFP constructs
Description Cloning Maps
1 Receiver cell construct for GFP diffusion experiments [http://parts.igem.org/Part:BBa_J09855 BBa_J09855] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_E0840 BBa_E0840] insert (XbaI, PstI) Map1.png
2 Library of the Receiver cell constructs Using the BBa_J09855-E0840 construct a library with mutated pLux promoters was created through site-saturation mutagenesis to screen for promoters with changed sensitivities for OHHL: Map2.png
3 Receiver cell construct for GFP experiments without the LuxR generating part [http://parts.igem.org/Part:BBa_R0062 BBa_R0062] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_E0840 BBa_E0840] insert (XbaI, PstI) Map3a.png
Map3b.png



LuxI generating constructs
Description Cloning Maps
4 Sender cell construct with a very strong constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments [http://parts.igem.org/Part:BBa_J23100 BBa_J23100] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI) Map4b.png
Map4a.png
5 Sender cell construct with an intermediate constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments [http://parts.igem.org/Part:BBa_J23118 BBa_J23118] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI) Map4b.png
Map4a.png
Map5c.png
6 Sender cell construct with an intermediate constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments [http://parts.igem.org/Part:BBa_J23110 BBa_J23110] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI) Map4b.png
Map4a.png
Map5c.png
7 Sender cell construct with a weak constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments [http://parts.igem.org/Part:BBa_J23114 BBa_J23114] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI) Map4b.png
Map4a.png


LuxR generating constructs
Description Cloning Maps
8 constitutive LuxR generating biobrick [http://parts.igem.org/Part:BBa_J09855 BBa_J09855] Map8.png
9 constitutive LuxR generating biobrick, with negative feedback-loop at high OHHL concentrations [http://parts.igem.org/Part:BBa_F2621 BBa_F2621] Map9.png
10 constitutive LuxR generating construct, repressible through LacI [http://parts.igem.org/Part:BBa_R0010 BBa_R0010] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_I0462 BBa_I0462] insert (XbaI, PstI) Map10.png
11 constitutive LuxR generating construct, with negative feedback-loop at high OHHL concentrations [http://parts.igem.org/Part:BBa_R0063 BBa_R0063] backbone (SpeI,PstI) and [http://parts.igem.org/Part:BBa_I0462 BBa_I0462] insert (XbaI, PstI) Map11.png
12 auto-inducible LuxR generating construct with positive feedback loop [http://parts.igem.org/Part:BBa_R0062 BBa_R0062] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_I0462 BBa_I0462] insert (XbaI, PstI) Map12.png
13 negatively regulated pLuxL-LacI construct to improve leakiness of LuxR system [http://parts.igem.org/Part:BBa_R0063 BBa_R0063] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_C0012 BBa_C0012] insert (SpeI,PstI) Map13.png



pLux constructs
Description Cloning Maps


Hydrolase constructs
Description Cloning Maps