Difference between revisions of "Team:Newcastle/MedalRequirements Jack"

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           <td>
 
           <td>
 
             <ul>
 
             <ul>
−
               <li><a href="http://parts.igem.org/Part:BBa_K2205002"><b>BBa_K2205002 - J23100-deGFP</b></a>
+
               <li style="margin-left:1%"><a href="http://parts.igem.org/Part:BBa_K2205002"><b>BBa_K2205002 - J23100-deGFP</b></a>
 
                 <ul>
 
                 <ul>
−
                   <li>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.</li>
+
                   <li style="margin-left:1%">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.</li>
−
                   <li>This part was made to be one of the potential reporter modules in our multicellular biosensor framework.</li>
+
                   <li style="margin-left:1%">This part was made to be one of the potential reporter modules in our multicellular biosensor framework.</li>
 
                 </ul>
 
                 </ul>
 
               </li>
 
               </li>
−
               <li><a href="http://parts.igem.org/Part:BBa_K2205004"><b>BBa_K2205004 - T7-Sarcosine Oxidase</b></a>
+
               <li style="margin-left:1%"><a href="http://parts.igem.org/Part:BBa_K2205004"><b>BBa_K2205004 - T7-Sarcosine Oxidase</b></a>
 
                 <ul>
 
                 <ul>
−
                   <li>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.</li>
+
                   <li style="margin-left:1%">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.</li>
−
                   <li>This part was made to be one of the potential adapter modules in our multicellular biosensor framework.</li>
+
                   <li style="margin-left:1%">This part was made to be one of the potential adapter modules in our multicellular biosensor framework.</li>
 
                 </ul>
 
                 </ul>
 
               </li>
 
               </li>
−
               <li><a href="http://parts.igem.org/Part:BBa_K2205009"><b>BBa_K2205009</a>, <a href="http://parts.igem.org/Part:BBa_K2205012">BBa_K2205012</a>, and <a href="http://parts.igem.org/Part:BBa_K2205015">BBa_K2205015</a> - Sensynova Multicellular biosensor Framework Modules </b>
+
               <li style="margin-left:1%"><a href="http://parts.igem.org/Part:BBa_K2205009"><b>BBa_K2205009</a>, <a href="http://parts.igem.org/Part:BBa_K2205012">BBa_K2205012</a>, and <a href="http://parts.igem.org/Part:BBa_K2205015">BBa_K2205015</a> - Sensynova Multicellular biosensor Framework Modules </b>
 
                 <ul>
 
                 <ul>
−
                   <li>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 or our results page to see full experimental data.</li>
+
                   <li style="margin-left:1%">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 or our results page to see full experimental data.</li>
 
                 </ul>
 
                 </ul>
 
               </li>               
 
               </li>               
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             Sensynova was a project founded in Human Practices. Each branch of our project is rooted in a barrier to biosensor implementation identified by in-depth conversations with stakeholders. We identified not only technical issues, but also societal issues, as these are equally important in ensuring successful implementation of biosensor projects. The aims of our human practices were to:
 
             Sensynova was a project founded in Human Practices. Each branch of our project is rooted in a barrier to biosensor implementation identified by in-depth conversations with stakeholders. We identified not only technical issues, but also societal issues, as these are equally important in ensuring successful implementation of biosensor projects. The aims of our human practices were to:
 
             <ol>
 
             <ol>
−
               <li>Determine how current biosensor developers design, produce and implement biosensor projects</li>
+
               <li style="margin-left:1%">Determine how current biosensor developers design, produce and implement biosensor projects</li>
−
               <li>Use these talks to determine the common barriers to biosensor development and implementation</li>
+
               <li style="margin-left:1%">Use these talks to determine the common barriers to biosensor development and implementation</li>
−
               <li>Create novel solutions to identified problems, producing frameworks and guidelines to aid future researchers</li>
+
               <li style="margin-left:1%">Create novel solutions to identified problems, producing frameworks and guidelines to aid future researchers</li>
 
             </ol>
 
             </ol>
 
             To achieve these aims, we emailed, skyped and attended conferences to speak to stakeholders in biosensor development, from the early research stage to the end-user. Check out our <a href="https://2017.igem.org/Team:Newcastle/HP/Gold_Integrated">integrated human practices page</a> for more information
 
             To achieve these aims, we emailed, skyped and attended conferences to speak to stakeholders in biosensor development, from the early research stage to the end-user. Check out our <a href="https://2017.igem.org/Team:Newcastle/HP/Gold_Integrated">integrated human practices page</a> for more information
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           <td>
 
           <td>
 
             <ul>
 
             <ul>
−
               <li><a href="http://parts.igem.org/Part:BBa_K2205026"><b>BBa_K2205026</a> - pSB1A51 (Promoter Library Screening Plasmid) - Improvement over <a href="http://parts.igem.org/Part:BBa_J61002">BBa_J61002</a> </b>
+
               <li style="margin-left:1%"><a href="http://parts.igem.org/Part:BBa_K2205026"><b>BBa_K2205026</a> - pSB1A51 (Promoter Library Screening Plasmid) - Improvement over <a href="http://parts.igem.org/Part:BBa_J61002">BBa_J61002</a> </b>
 
                 <ul>
 
                 <ul>
−
                   <li>Transcriptional insulation added before promoter cloning site (PCS)</li>
+
                   <li style="margin-left:1%">Transcriptional insulation added before promoter cloning site (PCS)</li>
−
                   <li><i>lac</i> operator added after PCS for additional characterisation ability</li>
+
                   <li style="margin-left:1%"><i>lac</i> operator added after PCS for additional characterisation ability</li>
−
                   <li>RBS cloning site added to allow testing of promoters with any desired RBS</li>
+
                   <li style="margin-left:1%">RBS cloning site added to allow testing of promoters with any desired RBS</li>
−
                   <li>mRFP1 CDS replaced with the CDS for the more fluorescent sfGFP</li>
+
                   <li style="margin-left:1%">mRFP1 CDS replaced with the CDS for the more fluorescent sfGFP</li>
−
                   <li>Promoters can easily be removed from pSB1A51 and assembled into another plasmid/with another BioBrick using BioBrick assembly</li>
+
                   <li style="margin-left:1%">Promoters can easily be removed from pSB1A51 and assembled into another plasmid/with another BioBrick using BioBrick assembly</li>
 
                 </ul>
 
                 </ul>
 
               </li>
 
               </li>
−
               <li><a href="http://parts.igem.org/Part:BBa_K2205005"><b>BBa_K2205004</a> - Fim Standby Switch - Improvement over <a href="http://parts.igem.org/Part:BBa_K1632007">BBa_K1632007</a></b>
+
               <li style="margin-left:1%"><a href="http://parts.igem.org/Part:BBa_K2205005"><b>BBa_K2205004</a> - Fim Standby Switch - Improvement over <a href="http://parts.igem.org/Part:BBa_K1632007">BBa_K1632007</a></b>
 
                 <ul>
 
                 <ul>
−
                   <li>Replaced E0040 CDS with eforRed chromoprotein CDS to allow easy visualisation with the naked eye</li>
+
                   <li style="margin-left:1%">Replaced E0040 CDS with eforRed chromoprotein CDS to allow easy visualisation with the naked eye</li>
−
                   <li>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)</li>
+
                   <li style="margin-left:1%">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)</li>
−
                   <li>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)</li>
+
                   <li style="margin-left:1%">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)</li>
 
                 </ul>
 
                 </ul>
 
               </li>             
 
               </li>             

Revision as of 20:39, 28 October 2017

spacefill

Medal Requirements

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 – Register for iGEM and attend the Giant Jamboree.
  • 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 or our results page to see full experimental data.
2 Collaboration – Meet all the deliverables on the Competition Deliverables page 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 – Create a page on your team wiki with clear attribution of each aspect of your project. Our human practices work has focused on addressing technology uptake, which is one of the challenges that we identified to biosensor development and deployment. This took place in three main stages. First, we determined the current state of dialogue by consulting previous dialogue studies and reviewing how language is used in the media. We then generated our own guidelines to help future researchers to develop dialogue in a constructive way. Finally, we put this into practise by creating activities and sharing our work in a way that established a dialogue and encouraged discussion. Check out our Human Practices (Silver) page for more information.
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. Sensynova was a project founded in Human Practices. Each branch of our project is rooted in a barrier to biosensor implementation identified by in-depth conversations with stakeholders. We identified not only technical issues, but also societal issues, as these are equally important in ensuring successful implementation of biosensor projects. The aims of our human practices were to:
  1. Determine how current biosensor developers design, produce and implement biosensor projects
  2. Use these talks to determine the common barriers to biosensor development and implementation
  3. Create novel solutions to identified problems, producing frameworks and guidelines to aid future researchers
To achieve these aims, we emailed, skyped and attended conferences to speak to stakeholders in biosensor development, from the early research stage to the end-user. Check out our integrated human practices page for more information
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_K2205004 - 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. Our Attributions page is here.
4 Demonstrate your work – Convince the judges that your project works. Our team participated in the Interlab Measurement Study.