Team:TU-Munich/Team/Collaborations
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==Collaboration with Dundee iGEM team== | ==Collaboration with Dundee iGEM team== | ||
+ | The iGEM team [https://2013.igem.org/Team:Dundee Dundee] 2013 also decided to work on bioremediation. They identified the toxin microcystein, which becomes typically released into water after algal blooms caused by cyanobacteria. This cyclic peptide toxin binds covalently the protein phosphatases type 1 (PP1) and is therefore toxic for mammals. The idea of the Dundee iGEM team is to express the PP1 protein as a absorber for microcystin in the environment. We received their PP1 BioBrick, will convert it from RFC 10 to RFC 25, construct some expression plasmids and transform ''Physcomitrella patens'' in order to have the Dundee's molecular mop in a aquatic, photoautotrophic chassis in order to expand the applicability of their project. | ||
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Revision as of 16:18, 25 June 2013
Help with BioBricks
- We received fluorescent proteins GFP, mKate2 and mVenus from the 2012 Team of LMU Munich.
- We have sent our pTUM100 vector system from 2012 to the iGEM Team of Tuebingen.
- We have provided the iGEM Team Uppsala with the BioBricks for the enzymes x, y and z.
Collaboration with Dundee iGEM team
The iGEM team Dundee 2013 also decided to work on bioremediation. They identified the toxin microcystein, which becomes typically released into water after algal blooms caused by cyanobacteria. This cyclic peptide toxin binds covalently the protein phosphatases type 1 (PP1) and is therefore toxic for mammals. The idea of the Dundee iGEM team is to express the PP1 protein as a absorber for microcystin in the environment. We received their PP1 BioBrick, will convert it from RFC 10 to RFC 25, construct some expression plasmids and transform Physcomitrella patens in order to have the Dundee's molecular mop in a aquatic, photoautotrophic chassis in order to expand the applicability of their project.
Collaboration with Paris-Saclay iGEM team
The iGEM team Paris_Saclay
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