Team:ETH Zurich/Experiments
From 2013.igem.org
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 |
Pcons 1 (Strong) | J23100 |
Pcons 2 | J23118 |
Pcons 3 | J23110 |
Pcons 4 (Weak) | J23114 |
Mutagenized promoter 1 ( low [AHL]) |
Optimized Biobrick ! |
Mutagenized promoter 2 ( middle [AHL]) |
Optimized Biobrick ! |
Mutagenized promoter 3 ( high [AHL]) |
Optimized Biobrick ! |
pLuxR | R0062 |
Plux | |
Plac | |
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
Enzyme-substrate reactions
We have cloned fluorescent receiver systems as backup for our circuit in case the hydrolase reaction do not work properly.
The enzyme substrate reactions take less than 5 minutes and are visible by eye.
Our minesweeper become better and better so keep on track for updates !
Hydrolase | Complementary substrate / IUPAC name | Visible color | ||
---|---|---|---|---|
LacZ | Beta-Galactosidase | X-Gal | 5-Bromo-4chloro-3-indolyl-beta-galactopyranoside | Blue |
LacZ | Beta-Galactosidase | Green-beta-D-Gal | N-Methyl-3-indolyl-beta-D_galactopyranoside | Green |
GusA | Beta-glucuronidase | Magenta glucuronide | 6-chloro-3-indolyl-beta-D-glucuronide-cycloheylammonium salt | Red |
PhoA | Alkaline phosphatase | pNPP | 4-Nitrophenylphosphatedi(tris) salt | Yellow |
Aes | Carboxyl esterase | Magenta butyrate | 5-bromo-6-chloro-3-indoxyl butyrate | Magenta |
NagZ | Glycoside hydrolase | X-glucosaminide X-Glunac | 5-bromo-4-chloro-3-indolyl-N-acetyl-beta-D-glucosaminide | Blue |