Difference between revisions of "Team:Newcastle/MedalRequirements"

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At the beginning of iGEM, we created a <a href="https://static.igem.org/mediawiki/2017/2/27/T--Newcastle--BB_collab_flyer.png">flyer</a> showcasing the strengths of our team and the various ways we could help other teams. As a result of this, we were contacted by three teams: Edinburgh overgraduate team, Exeter, and Evry Paris-Saclay.
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At the beginning of iGEM, we created a <a href="https://static.igem.org/mediawiki/2017/2/27/T--Newcastle--BB_collab_flyer.png">flyer</a> showcasing the strengths of our team and the various ways we could help other teams. As a result of this, we were contacted by three teams: <a href="https://2017.igem.org/Team:Edinburgh_OG/Collaborations">Edinburgh overgraduate team</a>, <a href="https://2017.igem.org/Team:Exeter/Collaborations">Exeter</a>, and <a href="https://2017.igem.org/Team:Evry_Paris-Saclay/Collaborations#about">Evry Paris-Saclay</a>.
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For the Edinburgh team, we used our modelling knowledge to help fix their model. We aided the Exeter team by repeating one of their experiments, and they gathered single-cell fluorescence data for our deGFP construct using their FACS machine. Finally, Paris designed a novel psicose-regulated promoter to be used in a biosensor. We then incorporated their promoter into our framework so that many different variants of a psicose biosensor could be designed, made and tested.
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For the Edinburgh team, we used our modelling knowledge to help fix their model. We aided the Exeter team by repeating one of their experiments, and they gathered single-cell fluorescence data for our deGFP construct using their FACS machine. Finally, Paris designed a novel psicose-regulated promoter to be used in a biosensor. We then incorporated their promoter into our framework so that many different variants of a psicose biosensor could be designed, made and tested.<br />
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<a href="https://2017.igem.org/Team:Newcastle/Collaborations">Check out our collaboration page for more information</a>
 
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Revision as of 16:55, 28 October 2017

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Medal

Criteria

Explanation
Bronze All must be met
1 Register and Attend – Register for iGEM and attend the Giant Jamboree. Newcastle iGEM team has registered and will be attending the Giant Jamboree in Boston.
2 Deliverables – Meet all the deliverables on the Competition Deliverables page A team wiki, poster, presentation and project attributions were made. The safety form, judging form and registry pages were completed.
3 Attribution – Create a page on your team wiki with clear attribution of each aspect of your project. Our Attributions page is here.
4 Characterise/Contribution – Participate in the Interlab Measurement Study and/or improve the characterisation of an existing BioBrick Part or Device and enter this information on that part's Main Page in the Registry. Our team participated in the Interlab Measurement Study.
Silver All must be met
1 Validated Part/Validated Contribution – Convince the judges that at least one new BioBrick Part of your own design that is central to your project works as expected.

  • BBa_K2205002 - J23100-deGFP
    • We have BioBrick standardised the deGFP Green Fluorescent Protein (GFP) variant for the first time. We created an expression construct (J23100 promoter and B0034 RBS in front of deGFP) and characterised the deGFP. Check the registry page or our results page to see full experimental data.
    • This part was made to be one of the potential reporter modules in our multicellular biosensor framework.
  • BBa_K2205004 - T7-Sarcosine Oxidase
    • We have BioBrick standardised the sarcosine oxidase enzyme for the first time. We created an expression construct (T7 promoter and B0034 RBS in front of SOx CDS) and demonstrated that SOx is capable of catalysing the reaction of sarcosine to formaldehyde. Check the registry page or our results page to see full experimental data.
    • This part was made to be one of the potential adapter modules in our multicellular biosensor framework.
  • BBa_K2205009, BBa_K2205012, and BBa_K2205015 - Sensynova Multicellular biosensor Framework Modules
    • We have designed, standardised, and characterised three modules (IPTG detector, blank processor, and sfGFP reporter) to act as a proof-of-concept for our multicellular biosensor framework. We demonstrated that each module is able to accept its input molecule, and produce its output molecule as a result. Check the registry pages (BBa_K2205009, BBa_K2205012, and BBa_K2205015), or our results page to see full experimental data.
2 Collaboration – Convince the judges you have significantly worked with another registered iGEM team in a meaningful way.

At the beginning of iGEM, we created a flyer showcasing the strengths of our team and the various ways we could help other teams. As a result of this, we were contacted by three teams: Edinburgh overgraduate team, Exeter, and Evry Paris-Saclay. For the Edinburgh team, we used our modelling knowledge to help fix their model. We aided the Exeter team by repeating one of their experiments, and they gathered single-cell fluorescence data for our deGFP construct using their FACS machine. Finally, Paris designed a novel psicose-regulated promoter to be used in a biosensor. We then incorporated their promoter into our framework so that many different variants of a psicose biosensor could be designed, made and tested.

Check out our collaboration page for more information

3 Human Practices – Convince the judges you have thought carefully and creatively about whether your work is safe, responsible and good for the world. Link.
Gold At least 2 must be met
1 Integrated Human Practices – Expand on your silver medal activity by demonstrating how you have integrated the investigated issues into the design and/or execution of your project. Link.
2 Improve a previous part or project – Improve the function of an existing BioBrick Part or existing iGEM project and display your achievement on your wiki.

BBa_K2205026 - pSB1A51 (Promoter Library Screening Plasmid) - Improvement over BBa_J61002

  • Transcriptional insulation added before promoter cloning site (PCS)
  • lac operator added after PCS for additional characterisation ability
  • RBS cloning site added to allow testing of promoters with any desired RBS
  • mRFP1 CDS replaced with the CDS for the more fluorescent sfGFP
  • Promoters can easily be removed from pSB1A51 and assembled into another plasmid/with another BioBrick using BioBrick assembly

BBa_K2205005 - Fim Standby Switch - Improvement over BBa_K1632007

  • Replaced E0040 CDS with eforRed chromoprotein CDS to allow easy visualisation with the naked eye
  • Added RhlI CDS on the reverse strand upstream of the flipable promoter to allow modular addition of secondary reporter CDSs (can be added within same cell, or in a different cell of a multicellular communiuty)
    • Provides a 'dual reporter' which produces eforRed in its 'default' state (i.e. no signal detected), and a protein of choice in its 'on' state (i.e. when a signal is detected)

3 Model your project – Convince the judges your project's design and/or implementation is based on insight you have gained from modelling. We have modelled various aspects of our project, creating Simbiotics and COPASI models of the sensor development platform and a Design of Experiments model to optimise the cell free systems in our project. Details can be found here.
4 Demonstrate your work – Convince the judges that your project works. We have produced a functional multicellular biosensor based on bacterial quorum sensing. Each part has been tested and characterised singularly. The co-culture of the 3 bacterial types are proved to form a working biosensing device. More details can be found here.