Difference between revisions of "Team:Cambridge-JIC/Human Practices"

 
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     <center><h1 style="font-family:'Montserrat'; line-height:1.295em">HUMAN PRACTICES</h1></center>
 
     <center><h1 style="font-family:'Montserrat'; line-height:1.295em">HUMAN PRACTICES</h1></center>
 
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         <a href="#DIY" class="darkBlue" style="font-family: 'Pacifico'"><h2 style="text-align: center">DIY Bio-Commmunity</h3></a>
 
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         <a href="#makespace" class="darkBlue" style="font-family: 'Pacifico'"><h2 style="text-align: center">Bio-Makespace</h3></a>
 
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         <a href="#open" class="darkBlue" style="font-family: 'Pacifico'"><h2 style="text-align: center">Open Plant</h3></a>
 
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         <a href="#society" class="darkBlue" style="font-family: 'Pacifico'"><h2 style="text-align: center">Synthetic Biology Society</h3></a>
 
         <a href="#society" class="darkBlue" style="font-family: 'Pacifico'"><h2 style="text-align: center">Synthetic Biology Society</h3></a>
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        <a href="#colab" class="darkBlue" style="font-family: 'Pacifico'"><h2 style="text-align: center">coLAB OpenPlant</h3></a>
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         <h2 style="font-family:Pacifico ; text-align: center">DIY Bio-Commmunity</h2>
 
         <h2 style="font-family:Pacifico ; text-align: center">DIY Bio-Commmunity</h2>
 
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         <img src="https://static.igem.org/mediawiki/2016/6/62/T--Cambridge-JIC--HP1_1.png" alt="design/1.png" style="display:block; margin-left:auto; margin-right:auto; max-width:100%; max-height:100%">
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         <center><figcaption>Getting to know the Paris Bettencourt team</figcaption></center>
 
         <center><figcaption>Getting to know the Paris Bettencourt team</figcaption></center>
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         <p>On the weekend that English ferry ports ground to a halt, and travellers faced 14-hour delays, members of the iGEM Cambridge-JIC team defied these odds to reach Paris in the name of science. Rather, in the name of NightScience, an annual conference hosted by the CRI (Center de Recherches Interdisciplinaires) at the Cité des Sciences et de l’Industries which brought together synthetic biologists and innovative thinkers from around the world for two days of fascinating talks and workshops.</p>  
 
         <p>On the weekend that English ferry ports ground to a halt, and travellers faced 14-hour delays, members of the iGEM Cambridge-JIC team defied these odds to reach Paris in the name of science. Rather, in the name of NightScience, an annual conference hosted by the CRI (Center de Recherches Interdisciplinaires) at the Cité des Sciences et de l’Industries which brought together synthetic biologists and innovative thinkers from around the world for two days of fascinating talks and workshops.</p>  
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         <p>Given the opportunity to present our project at the conference along with this year’s Paris Bettencourt iGEM team, the resonance of this idea with the iGEM philosophy and experimental process was clear (though we can only hope our project “illuminates” the plant science community with the light of at least a few suns). It also applied to the projects of many participants we met during the conference from interdisciplinary labs, such as the CRI and the Waag Society in Amsterdam, and the Bio Makespace community.</p>
 
         <p>Given the opportunity to present our project at the conference along with this year’s Paris Bettencourt iGEM team, the resonance of this idea with the iGEM philosophy and experimental process was clear (though we can only hope our project “illuminates” the plant science community with the light of at least a few suns). It also applied to the projects of many participants we met during the conference from interdisciplinary labs, such as the CRI and the Waag Society in Amsterdam, and the Bio Makespace community.</p>
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        <img src="https://static.igem.org/mediawiki/2016/3/3d/T--Cambridge-JIC--HP1_2.png" style="display:block; margin-left:auto; margin-right:auto; max-width:100%; max-height:100%">
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        <center><figcaption>Presenting our project at the conference</figcaption></center>
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         <p>We were inspired by the DIY hacking culture of this community and wanted to lend our support through the engineering side of our project. By developing low-cost open source hardware for the transformation and growth of plant tissue samples, we hope to equip the DIY Bio community with the tools it needs to increase the use of plant chassis. Attracting people from a diverse range of backgrounds,  the Makespace community is a promising way to improve the interaction of non-scientists with the field of plant synthetic biology.</p>
 
         <p>We were inspired by the DIY hacking culture of this community and wanted to lend our support through the engineering side of our project. By developing low-cost open source hardware for the transformation and growth of plant tissue samples, we hope to equip the DIY Bio community with the tools it needs to increase the use of plant chassis. Attracting people from a diverse range of backgrounds,  the Makespace community is a promising way to improve the interaction of non-scientists with the field of plant synthetic biology.</p>
         <p>Since our return to Cambridge, we have continued the design of a growth facility and gene gun. Several of our team members are also in the process of establishing Cambridge’s first Bio Makespace, which we hope to support as a team with the hardware we are developing and outreach activities later this summer.</p>       
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         <p>Since our return to Cambridge, we have continued the design of a growth facility and gene gun. Several of our team members are also in the process of establishing Cambridge’s first Bio Makespace, which we hope to support as a team with the hardware we are developing and outreach activities later this summer.</p>
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        <img src="https://static.igem.org/mediawiki/2016/c/cc/T--Cambridge-JIC--HP1_3.png" style="display:block; margin-left:auto; margin-right:auto; max-width:100%; max-height:100%">
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        <center><figcaption>Day Science vs. Night Science - exploring Paris with other syn bio enthusiasts</figcaption></center>
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         <center><h2 style="font-family:Montserrat ; line-height:1.295em">Promoting Homoplasmy</h2></center>
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         <h2 style="font-family:Pacifico ; text-align: center">Bio-Makespace</h2>
         <p>The ultimate goal of the project is to achieve homoplasmy in Chlamydomonas chloroplasts much more quickly than the <span class="darkGreen">2-3 months</span> of repeated antibiotic selection currently taken — ideally, over the span of a single generation.</p>
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         <p>Biomakespace is an initiative of synthetic biology scientists, students and enthusiasts in Cambridge who are working hard to build a new community laboratory. We aim to have a friendly sharing space where scientists could meet engineers, physicists, computer scientists, medics and other professionals but even public, students and schools. They all could start working together on synthetic biology projects from this academic year already. The iGEM team got involved with establishing of the space, planning and propagation from the very beginning.</p>  
         <p>Our method relies on double transformation of Chlamydomonas chloroplast with a cassette-of-interest (CoI) and the <span class="darkGreen">highly customisable “driver” cassette</span> that we are developing. The “driver” could be easily adapted to any cassette-of-interest by changing the 20 nucleotide gRNA space (plus, if needed, homology regions 1 and 2). The organisation of the two cassettes is shown in the figure below:</p>
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         <p>A few of us are planning to share with other students what we have learned from synthetic biology over the summer by leading or participating projects based on cell-free systems there in the coming academic year under the flag of the new student-led <a href="http://cusbs.soc.srcf.net/" class="darkBlue" style="font-size:100%">Cambridge University Synthetic Biology Society</a></p>
        <img src="https://static.igem.org/mediawiki/2016/2/22/T--Cambridge-JIC--description1.png" alt="description/1.png" style="display:block; margin-left:auto; margin-right:auto">
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         <p>Emerging Biomakespace and similar community labs have also hugely motivated us for our hardware sub-projects as Biomakespace hasn’t initially considered working on plants and algae or their chloroplasts much. By offering our affordable hardware to them and similar community labs over the world we will facilitate further development of plant and algal synthetic biology and also work on chloroplasts. As an example biolistics is the only reliable way to transform chloroplasts of plants or algae. However costs of commercial gene guns are absolutely beyond what such labs can usually afford. We are offering a cheap and tested alternative opening a whole new range of possible projects for them.</p>
        <p>After transformation, <span class="darkGreen">Cas9 would repeatedly cut chloroplast genome</span> copies at the desired site of insertion, thereby promoting homologous recombination (HR). The cutting would continue until the gRNA homology in all of genome copies has been disrupted, which can only result when the cassette-of-interest is used as the template for HR. Non-homologous end-joining does not occur in chloroplasts, and so would not interfere. By the end of the process, all genome copies would have the cassette-of-interest, i.e. homoplasmy would be achieved.</p>
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         <center><h2 style="font-family:Pacifico">Official aims of Biomakespace:</h2></center>
         <p>We are taking <span class="darkGreen">safety considerations</span> very seriously. The “driver” cassette would not promote its own propagation, as Cas9 would only cut the genome between homologies 1 and 2. This means that the transformed algae would not pose any danger, even if accidentally released into the environment. Moreover, it may be possible (although further testing is still needing to confirm this) to get rid of the Cas9 gene altogether, by replating the cells onto antibiotic 1 only, once homoplasmy is confirmed. This would remove the selection pressure for the “driver”, which might then be lost.</p>
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         <h2 style="font-family:Montserrat ; text-align: center">A library of chloroplast parts in PhytoBrick standard</h2>
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          <li>Bring together biologists, engineers, technologists and others in the Cambridge area for meeting, co-working and socialising in a creative, cross-disciplinary, community-driven and safe environment.
         <p style="text-align:center">We are also developing a library of chloroplast genetic components, compatible with the recently developed and <span class="darkGreen">highly modular</span> PhytoBrick standard for the assembly of gene units. We have codon-optimised many of our parts (using the software developed by Saul Purton at UCL), and are checking their functionality. Limited by the 10-week duration of the iGEM project, we are unlikely to complete all the necessary experiments to verify our Cas9 strategy, but the library would also have a standalone value and enable future work in this area.</p>
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          <li>Provide a well-equipped space for practical biology and engineering of biology on a community membership basis.
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          <li>Support new and existing interdisciplinary collaborations for engineering biology, with a focus on promoting open technology and innovation.
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          <li>Raise awareness, understanding and participation in biology and engineering of biology in the Cambridge area through public engagement activities, education and training.
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          <li>Foster links with local industry and innovation organisations, building bridges between academia and bioenterprise.
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         <h2 style="font-family:Pacifico ; text-align: center">OpenPlant</h2>
         <h1 style="font-family:Montserrat ; text-align: center">HARDWARE</h1>
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         <h3 style="font-family:Pacifico ; text-align: center">Understanding the bottlenecks of plant synthetic biology and best practices for open science</h3>
         <p style="text-align:center">We are developing open-source hardware which could come at <span class="darkWhite">a fraction of the cost of commercially available</span> equivalents, extensively documenting assembly <span class="darkWhite">protocols online</span> to make them accessible to researchers with little or no electronic and mechanical experience. All documentation will include comprehensive part names and wiring diagrams. We are also in the process of uploading video tutorials to Instructables / <a target="_blank" href="https://www.youtube.com/watch?v=3eOXwO4fxds"><b>Youtube</b></a></p>
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        <p>Hosted at the John Innes Centre in Norwich, the OpenPlant Forum presented talks from some of the most exciting innovations and research developing in plant synthetic biology at this moment. The three-day event also featured panel discussions on predominant issues in this field, including a discussion on “Commercial opportunities and bottlenecks in the future of plant synthetic biology”, featuring the inventor of BioBricks and ‘godfather’ of synthetic biology, Tom Knight.</p>
 
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        <h2 style="font-family:Montserrat ; text-align: center">Biolistic Device (“gene gun”)</h2>
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        <img src="https://static.igem.org/mediawiki/2016/6/61/T--Cambridge-JIC--HP3_1.png" style="display:block; margin-left:auto; margin-right:auto; max-width:100%; max-height:100%">
        <p>One of the project aims is to design, build and document a full protocol for a low-cost gene gun. Biolistics is a particle bombardment technique widely used in a range of cell/tissue type transformations, capable of rapid delivery of multiple plasmids for transient or stable expression and without the use of carrier DNA. The high-velocity microparticles can penetrate plant cell walls, enabling <b>transformation of plastids</b> such as the chloroplast, which we will use in our project.</p>
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        <center><figcaption></figcaption></center>
        <p>As useful as this technique is, the cost of commercially-available biolistic systems can run into the tens of thousands of pounds, making them unattainable for smaller laboratories and the hobbyist Syn Bio community. Our design will feature similar functions to these systems, allowing optimisation of firing pressure, duration and distance from the target, but for just <b>1% of their cost</b>. The gene gun will be designed to use lower-cost consumable options, such as easily-replaceable CO2 cartridges.</p>
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        <p>The design will also incorporate <b>safety features</b> for the user, which are generally neglected in existing DIY designs available online. (1) It operates at 140 psi, while most similar designs online use 600-700 psi, and most commercial ones around 1350 psi, (2) all electronics are contained inside a box, so no electrical connections are exposed, (3) additional circuit fuses are included and are specifically rated for the current going through, (4) all components are tested separately for leaks and electrical safety.</p>
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        <p>This discussion raised the need for creating more efficient techniques for engineering plants into chassis for commercial production of biofuels and pharmaceuticals. This is something which we already aim to achieve as part of our project, through a standardised cas9 system for chloroplast engineering, which follows the phytobrick common syntax. Other relevant challenges were also raised in the discussion on “Reprogramming Agriculture”, such as responsible research and public perception of plant synthetic biology. Members of our team took part in this talk, sharing our views with an audience of over 100 people and making the key point that scientists have a responsibility to document their research and methods thoroughly. Mistrust and misunderstanding of what plant synthetic biology will be used for, and the ownership of this technology, is a result of miscommunication between the scientific and nonscientific communities.</p>
        <h2 style="font-family:Montserrat ; text-align: center">Growth facility</h2>
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        <p>The discussions highlighted the importance of DIY Bio Hackspaces, such as those we had encountered at the Bio NightScience event in Paris. By allowing ‘ordinary’ citizens to actively participate in synthetic biology projects for themselves, this helps to bridge the gap between the two communities and create a dialogue between them. This further encouraged our design of a low cost growth facility and gene gun for such spaces, as any techniques for plant engineering which industry hopes to commercialise must first be widely accepted in the public eye. Providing accessibility to these techniques for hackspaces, schools and other small community labs will, we hope, promote more widespread understanding and acceptance of them.</p>
        <p style="text-align:center">Within the field of synthetic biology, there has recently been a necessity for low-cost, DIY, biological lab equipment in order to maintain the momentum at which the field is developing. Our iGEM team has two solutions to this problem, one of which is the growth chamber. Our team’s growth chamber allows you to optimise the conditions and to record and analyse the growth of your 90 mm petri dishes at a fraction of the cost of the commercially available equivalents, regardless of the samples you're growing</p>
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        <p>Furthermore, hearing Tobias Wenzel, founder of Docubricks, speak at the OpenPlant Forum gave us the idea to use this format as a template for the documentation of our open source designs. We hope that integrating the same best practices for open documentation used by this site into our own project will help to further support our efforts in removing the bottlenecks to chloroplast engineering, by changing public reaction and accessibility to the technology.</p>
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        <h2 style="font-family:Pacifico ; text-align: center">Synthetic Biology Society</h2>
          <h1 style="font-family:Montserrat ; text-align:center">Hardware Specification</h1>
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        <p>Synthetic biology society is a group of students at the University of Cambridge aiming to bring together biologists, engineers, physicists, computer scientists and others to work in synthetic biology and share knowledge. It has been established by previous iGEM members in 2015. The society has ambitions to raise awareness about synthetic biology amongst students, broaden their knowledge through talks and as probably the only Cambridge science society it is actively working on primary research projects.</p>  
          <h2 style="font-family:Montserrat ; text-align:center">Gene Gun</h2>
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        <p>A few of our members got involved over the year with society’s activities and helped a bit with its beginnings and Lucie is on the current committee as the project manager. Last year’s project still in progress involves building a computer-navigated microscope moving in all three dimensions and scanning samples. Apart from continuing this we are planning a wetlab project in Biomakespace (have a link) which wants to explore cell-free systems. The project may change slightly but we want to make and tune a simple light oscillator (probably using fluorescent proteins fused to luciferase for sharper output changes) and also build a physical electric circuit imitating the biological system. From there we can study and demonstrate if the two systems behave and can be regulated similarly or differently, which may have a big educational value, we could also concentrate on transferring the system into a living organism or even some design using multiple oscillators. The emphasis in the project will be put on sharing skills, learning (even through seminars and trainings) and exploring what synthetic biology and scientific work in a team are all about!</p>
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          <li>Total cost <£250 (1% of PDS-1000 retail price) – the final cost will be close to <b>£228.05</b>, with just the safety shield for the gun left to assemble.
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          <li>Generate pressure pulse of at least 100 psi
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          <li>Adjustable pulse pressure – maximum pressure of 10 bar.
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          <li>Adjustable pulse duration – minimum pulse of 50 ms, adjustable in 10 ms increments.
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          <li>Display pressure of firing pulse.
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          <li>Contain all electrical connections and wiring within an insulated box, ensuring there are no exposed electrical connections to pose risk to the user.
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          <li>Easily adjustable distance of gene gun from target plate.
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          <li>Provide measurement of distance from target plate using an adjacently-clamped ruler.
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          <li>Suspend carrier particles on a parafilm membrane which ruptures at the target pressure.
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          <li>Removable macrocarrier to hold the microparticles and membrane.
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          <li>Mesh filter in gun nozzle to prevent ruptured parafilm being fired into the target.
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          <li>Easily-replaceable supply of CO2, using generic threaded 16g CO2 cartridges
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          <li>Manual firing switch away from the actual gun, for safer firing.
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          <li>Successfully transform plant cell target at the low pressure levels generated by the gun, relative to commercial gene guns.
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          <li>Safety screen around gun to shield user from ruptured membrane debris. This will fit over the electronics box and gun trigger when stored, so the user must consciously handle the safety screen before firing the gun and will thus be reminded to use this safety feature.
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          <li>Base to provide stability for the gun and petri dishes of different sizes.
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          <li>Easy to surface sterilise the gun and base for use in sterile fume hood.
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          <p style="text-align:center">We plan to test the gun in early September by transforming onion bulb cells with a GFP or GUS reporter system, experimenting with optimisation of the firing pressure for the gun and documenting penetration of the cell target qualitatively.</p>
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          <p style="text-align:center">The connections in the gun are all currently being pressure tested under water and sealed using PTFE tape, to ensure the gun is safe for repeated use.</p>
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          <img src="https://static.igem.org/mediawiki/2016/6/64/T--Cambridge-JIC--design1.png" alt="design/1.png" style="display:block; margin-left:auto; margin-right:auto">
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          <h2 style="font-family:Montserrat ; text-align:center">General layout of the gene gun</h2>
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          <li>The gun is mounted on a clamp stand and wooden base, with all the electronics contained inside the box on the left (the gun would go inside the sterile fume hood and the box could be left on the bench outside). The stand height has been reduced to 0.4m so it can fit inside any standard sterile hood.
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          <li>The final prototype will also include a ruler clamped alongside the gun to measure distance to the target plate on firing.
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          <li>The wires connecting the box to the gun are 0.6m long, to allow the electronics to remain contained and outside of the sterile hood during transformations (reducing the risk of liquid disinfectant being sprayed on any electrical connections).
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          <img src="https://static.igem.org/mediawiki/2016/6/65/T--Cambridge-JIC--design2.png" alt="design/2.png" style="display:block; margin-left:auto; margin-right:auto">
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          <img src="https://static.igem.org/mediawiki/2016/e/ec/T--Cambridge-JIC--design3.png" alt="design/3.png" style="display:block; margin-left:auto; margin-right:auto">
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         <h1 style="font-family:Montserrat ; text-align: center">Growth Facility</h1>
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         <h2 style="font-family:Pacifico ; text-align: center">coLAB OpenPlant</h2>
         <h2 style="font-family:Montserrat ; text-align: center">Design Aims</h2>
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         <h3 style="font-family:Pacifico ; text-align: center">Investigating perceptions of plant biotech</h3>
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         <p>In June, we spent three days taking part in the CoLAB OpenPlant Cambridge workshop, held in the University Plant Sciences Department. We engaged in and led discussions about the ethics of synthetic biology during the workshop, involving participants from 10+ countries with a variety of backgrounds, including art & design, medicine, music and biological sciences. As a part of the workshop, we learnt about the different techniques of investigating public perception and understanding, such as providing unexpected physical stimuli in typical environments and observing people’s reactions.</p>
        <li>10 high-power LEDs (up to around 2 Watts each), with 2 each of 5 different colours (red, true green, blue, ultra-white 6000K, and infrared 850nm) that can be programmed in circadian rhythms, allowing you to choose the wavelength and the intensity of light that is best for your samples
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         <p>This culminated in us conducting our own surveys on the streets of Cambridge on deliberately thought-provoking issues surrounding plant biotech, to establish a dialogue with the public about plant synthetic biology and understand the opinions already held about this area. Some of the issues we investigated included the ethics of plant experimentation, comparing this with animal testing and seeing if similar emotional responses could be generated from questions such as ‘Do plants feel pain?’</p>
        <li>A “Peltier” element for temperature control
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         <p>We also investigated how people felt about potential future applications of plant syn bio, such as enhancing the nutritional content of certain foods, or even using engineered plants to express a person’s complete nutritional requirements which could then be extracted and concentrated into a pill-a-day form.</p>
        <li>A camera module controlled by a Raspberry Pi which autonomously takes pictures of your samples at pre-scheduled intervals and uploads them online, allowing you to view the progress of your samples from anywhere with an internet connection (and also to produce time-lapses)
+
         <p>Although many of our questions were purely hypothetical, the conversations they generated were eye opening for us in understanding the reasoning behind some objections to plant syn bio. Participating in the workshop at this early stage in our project ensured we considered the impact of our work on different communities, and the potential reactions to the technology that could stem from the project, throughout the entire iGEM process.</p>
        <li>A thermistor and LDR for measurement and analysis of temperature and light conditions throughout growth (the growth chamber produces tables of this information which can be imported into Excel), as well as for feedback to the “Peltier” element
+
        <br> 
        <li>Fans for controlling air circulation in the growth chamber, and for cooling electronic components
+
        <ul>
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+
        <hr>
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        <p style="text-align:center">The design of this growth facility is currently being documented, and will be published in a full tutorial on Instructables and our wiki, with the intention that anyone who wants to will be able to find the tutorial and follow it without difficulty, regardless of experience.</p
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        <h2 style="font-family:Montserrat ; text-align: center">Extendibility</h2>
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         <p style="text-align:center">This growth chamber houses <span class="darkWhite">1 petri dish</span>. The reason I made this design decision was that housing multiple petri dishes in the same growth chamber would have resulted in inconsistent conditions in temperature and lighting (and larger material costs), whereas having multiple chambers joined together wouldn’t have had any obvious advantages over building several separate units, in order to justify the extra material costs and effort required under the time pressure.</p>
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        <p style="text-align:center">If one wanted to house several petri dishes, the options would be to either build separate units, or to modify the CAD files and acquire extra components (the CAD files will be uploaded to the wiki and Instructables along with the tutorial) in order to house the extra petri dishes.</p>
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         <h2 style="font-family:Montserrat ; text-align: center">Possible improvements</h2>
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        <ul>
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        <li>Improve efficiency of Peltier element by adding extra fan to remove air from the “hot side”
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        <li>Add H-bridge, allowing the Peltier to be controlled as both a heater and a cooler
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        <li>Acquire a higher-power Peltier element
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        <li>Improve organisation of wiring
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        <ul>
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        <h2 style="font-family:Montserrat ; text-align: center">Power Supplies</h2>
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         <p style="text-align:center">It was originally intended to house both the 5V power supply and the 700mA LED driver within the electronics enclosure, however, due to Jake's hastiness with soldering, Jake accidentally soldered the LED driver to the mains cable before putting the mains cable through the hole for external cabling, so that the LED driver now doesn’t fit through the hole. Hence Jake decided to keep the power supplies outside of the box. Jake will resolve this issue for the future by modifying the CAD files so that the hole meets the top of the box.</p>
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        <h2 style="font-family:Montserrat ; text-align: center">Main View</h2>     
 
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        <h2 style="font-family:Montserrat ; text-align: center">Inside View</h2>     
 
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        <h2 style="font-family:Montserrat ; text-align: center">Electronic Enclosure</h2>     
 
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        <h2 style="font-family:Montserrat ; text-align: center">Power Supplies</h2>     
 
          <img src="https://static.igem.org/mediawiki/2016/2/28/T--Cambridge-JIC--design7.png" alt="design/7.png" style="display:block; margin-left:auto; margin-right:auto">
 
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Latest revision as of 21:29, 15 October 2016

Cambridge-JIC

HUMAN PRACTICES



DIY Bio-Commmunity

Getting to know the Paris Bettencourt team

On the weekend that English ferry ports ground to a halt, and travellers faced 14-hour delays, members of the iGEM Cambridge-JIC team defied these odds to reach Paris in the name of science. Rather, in the name of NightScience, an annual conference hosted by the CRI (Center de Recherches Interdisciplinaires) at the Cité des Sciences et de l’Industries which brought together synthetic biologists and innovative thinkers from around the world for two days of fascinating talks and workshops.

The event follows the philosophy of Night Science from the French biologist François Jacob, winner of the 1965 Nobel Prize for Medicine for his joint discovery of transcriptional regulation of enzyme level expression by the lac operon in E.coli. He proposed the concept of Night Science in his 1988 memoir “The Statue Within”, writing:

“Science has in fact two aspects. Day science involves reasoning as articulated as gears, results that have the strength of certainty…
Night Science, on the contrary, wanders in the dark. It hesitates, stumbles, falls. Questioning everything... Nothing guarantees its successes, its ability to survive the tests of logic and experiments, but sometimes thanks to intuition, instinct and the will to discover, as a lightning it illuminates more than a thousand suns…”.

Given the opportunity to present our project at the conference along with this year’s Paris Bettencourt iGEM team, the resonance of this idea with the iGEM philosophy and experimental process was clear (though we can only hope our project “illuminates” the plant science community with the light of at least a few suns). It also applied to the projects of many participants we met during the conference from interdisciplinary labs, such as the CRI and the Waag Society in Amsterdam, and the Bio Makespace community.

Presenting our project at the conference

We were inspired by the DIY hacking culture of this community and wanted to lend our support through the engineering side of our project. By developing low-cost open source hardware for the transformation and growth of plant tissue samples, we hope to equip the DIY Bio community with the tools it needs to increase the use of plant chassis. Attracting people from a diverse range of backgrounds, the Makespace community is a promising way to improve the interaction of non-scientists with the field of plant synthetic biology.

Since our return to Cambridge, we have continued the design of a growth facility and gene gun. Several of our team members are also in the process of establishing Cambridge’s first Bio Makespace, which we hope to support as a team with the hardware we are developing and outreach activities later this summer.

Day Science vs. Night Science - exploring Paris with other syn bio enthusiasts

Bio-Makespace

Biomakespace is an initiative of synthetic biology scientists, students and enthusiasts in Cambridge who are working hard to build a new community laboratory. We aim to have a friendly sharing space where scientists could meet engineers, physicists, computer scientists, medics and other professionals but even public, students and schools. They all could start working together on synthetic biology projects from this academic year already. The iGEM team got involved with establishing of the space, planning and propagation from the very beginning.

A few of us are planning to share with other students what we have learned from synthetic biology over the summer by leading or participating projects based on cell-free systems there in the coming academic year under the flag of the new student-led Cambridge University Synthetic Biology Society

Emerging Biomakespace and similar community labs have also hugely motivated us for our hardware sub-projects as Biomakespace hasn’t initially considered working on plants and algae or their chloroplasts much. By offering our affordable hardware to them and similar community labs over the world we will facilitate further development of plant and algal synthetic biology and also work on chloroplasts. As an example biolistics is the only reliable way to transform chloroplasts of plants or algae. However costs of commercial gene guns are absolutely beyond what such labs can usually afford. We are offering a cheap and tested alternative opening a whole new range of possible projects for them.

Official aims of Biomakespace:

  1. Bring together biologists, engineers, technologists and others in the Cambridge area for meeting, co-working and socialising in a creative, cross-disciplinary, community-driven and safe environment.
  2. Provide a well-equipped space for practical biology and engineering of biology on a community membership basis.
  3. Support new and existing interdisciplinary collaborations for engineering biology, with a focus on promoting open technology and innovation.
  4. Raise awareness, understanding and participation in biology and engineering of biology in the Cambridge area through public engagement activities, education and training.
  5. Foster links with local industry and innovation organisations, building bridges between academia and bioenterprise.


OpenPlant

Understanding the bottlenecks of plant synthetic biology and best practices for open science

Hosted at the John Innes Centre in Norwich, the OpenPlant Forum presented talks from some of the most exciting innovations and research developing in plant synthetic biology at this moment. The three-day event also featured panel discussions on predominant issues in this field, including a discussion on “Commercial opportunities and bottlenecks in the future of plant synthetic biology”, featuring the inventor of BioBricks and ‘godfather’ of synthetic biology, Tom Knight.


This discussion raised the need for creating more efficient techniques for engineering plants into chassis for commercial production of biofuels and pharmaceuticals. This is something which we already aim to achieve as part of our project, through a standardised cas9 system for chloroplast engineering, which follows the phytobrick common syntax. Other relevant challenges were also raised in the discussion on “Reprogramming Agriculture”, such as responsible research and public perception of plant synthetic biology. Members of our team took part in this talk, sharing our views with an audience of over 100 people and making the key point that scientists have a responsibility to document their research and methods thoroughly. Mistrust and misunderstanding of what plant synthetic biology will be used for, and the ownership of this technology, is a result of miscommunication between the scientific and nonscientific communities.

The discussions highlighted the importance of DIY Bio Hackspaces, such as those we had encountered at the Bio NightScience event in Paris. By allowing ‘ordinary’ citizens to actively participate in synthetic biology projects for themselves, this helps to bridge the gap between the two communities and create a dialogue between them. This further encouraged our design of a low cost growth facility and gene gun for such spaces, as any techniques for plant engineering which industry hopes to commercialise must first be widely accepted in the public eye. Providing accessibility to these techniques for hackspaces, schools and other small community labs will, we hope, promote more widespread understanding and acceptance of them.

Furthermore, hearing Tobias Wenzel, founder of Docubricks, speak at the OpenPlant Forum gave us the idea to use this format as a template for the documentation of our open source designs. We hope that integrating the same best practices for open documentation used by this site into our own project will help to further support our efforts in removing the bottlenecks to chloroplast engineering, by changing public reaction and accessibility to the technology.


Synthetic Biology Society

Synthetic biology society is a group of students at the University of Cambridge aiming to bring together biologists, engineers, physicists, computer scientists and others to work in synthetic biology and share knowledge. It has been established by previous iGEM members in 2015. The society has ambitions to raise awareness about synthetic biology amongst students, broaden their knowledge through talks and as probably the only Cambridge science society it is actively working on primary research projects.

A few of our members got involved over the year with society’s activities and helped a bit with its beginnings and Lucie is on the current committee as the project manager. Last year’s project still in progress involves building a computer-navigated microscope moving in all three dimensions and scanning samples. Apart from continuing this we are planning a wetlab project in Biomakespace (have a link) which wants to explore cell-free systems. The project may change slightly but we want to make and tune a simple light oscillator (probably using fluorescent proteins fused to luciferase for sharper output changes) and also build a physical electric circuit imitating the biological system. From there we can study and demonstrate if the two systems behave and can be regulated similarly or differently, which may have a big educational value, we could also concentrate on transferring the system into a living organism or even some design using multiple oscillators. The emphasis in the project will be put on sharing skills, learning (even through seminars and trainings) and exploring what synthetic biology and scientific work in a team are all about!

coLAB OpenPlant

Investigating perceptions of plant biotech

In June, we spent three days taking part in the CoLAB OpenPlant Cambridge workshop, held in the University Plant Sciences Department. We engaged in and led discussions about the ethics of synthetic biology during the workshop, involving participants from 10+ countries with a variety of backgrounds, including art & design, medicine, music and biological sciences. As a part of the workshop, we learnt about the different techniques of investigating public perception and understanding, such as providing unexpected physical stimuli in typical environments and observing people’s reactions.

This culminated in us conducting our own surveys on the streets of Cambridge on deliberately thought-provoking issues surrounding plant biotech, to establish a dialogue with the public about plant synthetic biology and understand the opinions already held about this area. Some of the issues we investigated included the ethics of plant experimentation, comparing this with animal testing and seeing if similar emotional responses could be generated from questions such as ‘Do plants feel pain?’

We also investigated how people felt about potential future applications of plant syn bio, such as enhancing the nutritional content of certain foods, or even using engineered plants to express a person’s complete nutritional requirements which could then be extracted and concentrated into a pill-a-day form.

Although many of our questions were purely hypothetical, the conversations they generated were eye opening for us in understanding the reasoning behind some objections to plant syn bio. Participating in the workshop at this early stage in our project ensured we considered the impact of our work on different communities, and the potential reactions to the technology that could stem from the project, throughout the entire iGEM process.