Team:ETH Zurich/Experiments

From 2013.igem.org

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Here we will paste some circuit designs
Here we will paste some circuit designs
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<b>Enzyme-substrate reactions</b>
 
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<hr>
 
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<p>We have cloned fluorescent receiver systems as backup for our circuit in case the hydrolase reaction do not work properly.<br>The enzyme substrate reactions take less than 5 minutes and are visible by eye.<br><br> Our minesweeper become better and better so keep on track for updates !</p>
 
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<table style="float:left;margin-top:10px">
 
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<tr>
 
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<th colspan="2">Hydrolase</th>
 
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<th colspan="2">Complementary substrate / IUPAC name</th>
 
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<th>Visible color</th>
 
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</tr>
 
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<tr>
 
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<td>LacZ</td>
 
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<td>Beta-Galactosidase</td>
 
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<td>X-Gal</td>
 
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<td>5-Bromo-4chloro-3-indolyl-beta-galactopyranoside</td>
 
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<td style="color:blue">Blue</td>
 
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</tr>
 
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<tr>
 
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<td>LacZ</td>
 
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<td>Beta-Galactosidase</td>
 
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<td>Green-beta-D-Gal</td>
 
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<td>N-Methyl-3-indolyl-beta-D_galactopyranoside</td>
 
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<td style="color:Green">Green</td>
 
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</tr>
 
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<tr>
 
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<td>GusA</td>
 
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<td>Beta-glucuronidase</td>
 
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<td>Magenta glucuronide</td>
 
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<td>6-chloro-3-indolyl-beta-D-glucuronide-cycloheylammonium salt</td>
 
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<td style="color:Red">Red</td>
 
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</tr>
 
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<tr>
 
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<td>PhoA</td>
 
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<td>Alkaline phosphatase</td>
 
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<td>pNPP</td>
 
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<td>4-Nitrophenylphosphatedi(tris) salt</td>
 
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<td style="color:Yellow">Yellow</td>
 
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</tr>
 
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<tr>
 
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<td>Aes</td>
 
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<td>Carboxyl esterase</td>
 
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<td>Magenta butyrate</td>
 
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<td>5-bromo-6-chloro-3-indoxyl butyrate</td>
 
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<td style="color:Magenta">Magenta</td>
 
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</tr>
 
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<tr>
 
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<td>NagZ</td>
 
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<td>Glycoside hydrolase</td>
 
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<td>X-glucosaminide X-Glunac</td>
 
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<td>5-bromo-4-chloro-3-indolyl-N-acetyl-beta-D-glucosaminide</td>
 
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<td style="color:Lightblue">Blue</td>
 
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</tr>
 
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</table>
 
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<br><br>
 
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[[File:Magenta_butyrate_on_aes_t7_strain.JPG|left|148px|thumb|Fig.1: Magenta butyrate on Aes expressing colony]]
 
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[[File:PNPP_on_phoA_t7_strain.JPG|left|200px|thumb|Fig.2: NPP on PhoA expressing colony]]
 
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[[File:Salmon_glcUA_on_gusA_t7_strain.JPG |left|180px|thumb|Fig.3 Magenta glucuronide on GusA colony]]
 
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[[File:XGlcNAc_on_nagZ_t7_strain.JPG|left|200px|thumb|Fig.4: X-Glucnac on NagZ colony]]
 
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[[File:XGlcNAc_on_nagZ_t7_strain.JPG|left|200px|thumb|Fig.5: X-Gal on LacZ colony]]
 
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[[File:XGlcNAc_on_nagZ_t7_strain.JPG|left|200px|thumb|Fig.5: Beta-green-X-gal on LacZ colony]]
 
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Revision as of 11:06, 26 August 2013

Header2.png
80px-Eth igem logo.png

Tranformation and cloning constructs


Sender cells Receiver cells
AHL expressing system Fluorescent reporter system Enzyme reaction-based reporter system
Pcons-LuxI 1 (Strong) Plac-LuxR-Plux-GFP Plac-LuxR-Plux-LacZ
Pcons-LuxI 2 Plac-LuxR-Plux-YFP Plac-LuxR-Plux-Aes
Pcons-LuxI 3 Plac-LuxR-Plux-CFP Plac-LuxR-Plux-GusA
Pcons-LuxI 4 (Weak) Plac-LuxR-Plux-PhoA
Plac-LuxR-Plux-NagZ
Biobrick Registry part
LuxI K805016
LuxR C0062
Pcons 1 (Strong) J23100
Pcons 2 J23118
Pcons 3 J23110
Pcons 4 (Weak) J23114
Mutagenized Plux
( low [AHL])
Optimized Biobrick !
Mutagenized Plux
( middle [AHL])
Optimized Biobrick !
Mutagenized Plux
( high [AHL])
Optimized Biobrick !
pLuxR R0062
Plac I14032
GFP E0840
YFP E0030
CFP E0020
LacZ I732006
GusA New Biobrick !
PhoA New Biobrick !
Aes New Biobrick !
NagZ New Biobrick !










Here we will paste some circuit designs