Team:ETH Zurich/Achievements
From 2011.igem.org
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* We improved the pSB6A1 Plasmid to standard 5: [http://partsregistry.org/Part:BBa_K625005 pSB6A5] | * We improved the pSB6A1 Plasmid to standard 5: [http://partsregistry.org/Part:BBa_K625005 pSB6A5] | ||
* We created the [http://partsregistry.org/Part:BBa_K625000 BioBrick LacI<sub>M1</sub>] which is a codon modified LacI for multiplasmid operations | * We created the [http://partsregistry.org/Part:BBa_K625000 BioBrick LacI<sub>M1</sub>] which is a codon modified LacI for multiplasmid operations | ||
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* We [[Team:ETH_Zurich/Process/Validation|sistematically came up with the current channel design]] through a [[Team:ETH_Zurich/Process/Microfluidics|process of developing and refining chain of ideas for different designs]]. | * We [[Team:ETH_Zurich/Process/Validation|sistematically came up with the current channel design]] through a [[Team:ETH_Zurich/Process/Microfluidics|process of developing and refining chain of ideas for different designs]]. | ||
* Modeling help to improved the channel design | * Modeling help to improved the channel design | ||
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* We presented Synthetic Biology and iGEM to our fellow students in the [[Team:ETH Zurich/Team/Human practices#7.10.11 CBB Get together afternoon|CBB get together afternoon]]. | * We presented Synthetic Biology and iGEM to our fellow students in the [[Team:ETH Zurich/Team/Human practices#7.10.11 CBB Get together afternoon|CBB get together afternoon]]. | ||
* We presented iGEM and our project to the general public on the [[Team:ETH Zurich/Team/Human practices#22.10.11 D-BSSE Open house|BSSE Open House Day]] through a poster and a slide show. | * We presented iGEM and our project to the general public on the [[Team:ETH Zurich/Team/Human practices#22.10.11 D-BSSE Open house|BSSE Open House Day]] through a poster and a slide show. | ||
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* xx managed to move the Dropbox folder to another location, thus making it look empty for the others. | * xx managed to move the Dropbox folder to another location, thus making it look empty for the others. | ||
* xx accidentally modified an other teams wiki for 1 min | * xx accidentally modified an other teams wiki for 1 min |
Revision as of 20:38, 27 October 2011
SmoColi - Achievements
General
- We came up with the idea of a bacterio-quantifier of smoke.
- We worked hard and presented our work during the Regional Jamboree in Amsterdam.
- We received an iGEM 2011 Gold Medal and were invited to advance to the World Championship in Cambridge, USA.
- We documented everything we did in our Wiki Website.
- We helped the Edinburgh 2011 iGEM team with debugging their MATLAB cellulase model.
Modeling
- We made a reaction-diffusion model for the toxic molecule gradient formation in a channel and got a feeling about the feasibility of our ideas and channel dimensions.
- We approximated the gradient analytically and checked that it almost coincides with the numerically obtained one.
- We made a single cell model describing our circuit and verified its operation.
- We performed a robustness analysis of our system to see how the band behaves upon parameter variations and concluded that it is robust and monostable.
- We performed stochastic analysis to see how the GFP band reacts upon noise and confirmed one more time its robustness
- We integrated the single cell model and the reaction-diffusion model in a combined 3D spatiotemporal reaction-diffusion model, simulated for various channel dimensions to get a feeling how the GFP band will move and how the alarm is activated
- We extracted some information about the channel dimensions from the model and used this information in the actual channel design.
Biology
- We improved the pSB6A1 Plasmid to standard 5: [http://partsregistry.org/Part:BBa_K625005 pSB6A5]
- We created the [http://partsregistry.org/Part:BBa_K625000 BioBrick LacIM1] which is a codon modified LacI for multiplasmid operations
- We created two improved version of the PU BioBrick
- We successfully tested the channel in terms of cell viability and GFP synthesis
- We could established a gradient of a small molecule (IPTG and arabinose) in a tube and also in the microfluidic channel
Microfluidics
- We sistematically came up with the current channel design through a process of developing and refining chain of ideas for different designs.
- Modeling help to improved the channel design
- We participated in the PDMS channel construction.
Human Practices
- We presented Synthetic Biology and iGEM to our fellow students in the CBB get together afternoon.
- We presented iGEM and our project to the general public on the BSSE Open House Day through a poster and a slide show.
- We also made a survey with critical questions related to Synthetic Biology and iGEM, asked people to fill it out and analyzed the results.
- ETH GLOBE and the NZZ (Neue Zeitung Zürich) will write about our participation at iGEM World Championship Jamboree
Personal achievements
- xx managed to move the Dropbox folder to another location, thus making it look empty for the others.
- xx accidentally modified an other teams wiki for 1 min
- xx and xy slept the whole boat trip in Amsterdam
- xy found a mistake in the PowerPoint in the morning before the presentation ("And the channel turns read")
- xy managed to sleep at two chairs in the lab
- We had fun!