Team:London BioHackspace

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<h1 >WELCOME TO iGEM 2014! </h1>
 
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<p>Your team has been approved and you are ready to start the iGEM season!
 
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<br>On this page you can document your project, introduce your team members, document your progress <br> and share your iGEM experience with the rest of the world! </p>
 
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<p style="color:#E7E7E7"> <a href="https://2014.igem.org/wiki/index.php?title=Team:London_BioHackspace&action=edit"style="color:#FFFFFF"> Click here  to edit this page!</a> </p>
 
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<a href="https://2014.igem.org/Team:London_BioHackspace"style="color:#000000">Home </a> </td>
 
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<a href="https://2014.igem.org/Team:London_BioHackspace/Team"style="color:#000000"> Team </a> </td>
 
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<a href="https://igem.org/Team.cgi?year=2014&team_name=London_BioHackspace"style="color:#000000"> Official Team Profile </a></td>
 
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<a href="https://2014.igem.org/Team:London_BioHackspace/Project"style="color:#000000"> Project</a></td>
 
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<a href="https://2014.igem.org/Team:London_BioHackspace/Protocols"style="color:#000000">Protocols</a></td>
 
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<p>We can then push the patterned layer of cellulose below the surface and project a new pattern of light onto the culture. If we repeat this process a three dimensional structure will be built up out of the numerous patterned layers.</p>
<p>We can then push the patterned layer of cellulose below the surface and project a new pattern of light onto the culture. If we repeat this process a three dimensional structure will be built up out of the numerous patterned layers.</p>
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<p> Please be sure to keep these links, your audience will want to find your: </p>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace">Home</a> </li>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace/Team">Team</a> </li>
 
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<li><a href="https://igem.org/Team.cgi?year=2013&team_name=London_BioHackspace">Official Team Profile</a> </li>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace/Project">Project</a> </li>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace/Parts">Parts</a> </li>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace/Modeling">Modeling</a> </li>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace/Notebook">Notebook</a> </li>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace/Safety">Safety</a> </li>
 
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<li><a href="https://2014.igem.org/Team:London_BioHackspace/Attributions">Attributions</a> </li>
 
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<li>All pages, images and files must be hosted on the <a href ="https://2014.igem.org/Special:Upload">  2014.igem.org server</a>. </li>
 
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<li>All pages must be created under the team’s name space.</li>
 
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<li>As part of your documentation, keep the links from the menu to the left. </li>
 
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<li>The <a href="https://static.igem.org/mediawiki/igem.org/6/60/Igemlogo_300px.png"> iGEM logo </a> should be placed on the upper part of every page and should link to <a href="https://2014.igem.org/Main_Page">2014.igem.org</a>.</li>
 
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<p>Visit the <a href="https://2014.igem.org/Wiki_How-To"> Wiki How To page </a> for a complete list of requirements, tips and other useful information. </p>
 
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<p>We are currently working on providing teams with some easy to use design templates.
 
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<br> In the meantime you can also view other team wikis for inspiration! Here are some very good examples</p>
 
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<li> <a href="https://2013.igem.org/Team:SDU-Denmark/"> 2013 SDU Denmark </a> </li>
 
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<li> <a href="https://2013.igem.org/Team:SYSU-China">2013 SYSU China</a> </li>
 
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<li> <a href="https://2013.igem.org/Team:Shenzhen_BGIC_ATCG"> 2013 Shenxhen BGIG ATCG </a></li>
 
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<li> <a href="https://2013.igem.org/Team:Colombia_Uniandes">2013 Colombia Unianades </a></li>
 
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<li> <a href="https://2013.igem.org/Team:Lethbridge">2013 Lethbridge</a></li>
 
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<p>For a full wiki list, you can visit <a href="https://igem.org/Team_Wikis?year=2013">iGEM 2013 web sites </a> and <a href="https://igem.org/Team_Wikis?year=2012">iGEM 2012 web sites</a>  lists. </p>
 
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<p>This wiki will be your team’s first interaction with the rest of the world, so here are a few tips to help you get started: </p>
 
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<li>State your accomplishments! Tell people what you have achieved from the start. </li>
 
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<li>Be clear about what you are doing and what you plan to do.</li>
 
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<li>You have a global audience! Consider the different backgrounds that your users come from.</li>
 
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<li>Make sure information is easy to find; nothing should be more than 3 clicks away.  </li>
 
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<li>Avoid using very small fonts and low contrast colors; information should be easy to read.  </li>
 
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<li>Start documenting your project as early as possible; don’t leave anything to the last minute before the Wiki Freeze. For a complete list of deadlines visit the <a href="">iGEM 2013 calendar</a> </li>
 
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<li>Have lots of fun! </li>
 
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Latest revision as of 03:09, 18 October 2014

Home Project Team Policy & Practice Protocols Safety

Project Description: JuicyPrint

What is JuicyPrint?

JuicyPrint will be a 3d printer that can be fed with fruit juice and can be used to print out useful shapes made of bacterial cellulose, a strong and exceptionally versatile biopolymer.

Why bacterial cellulose?

Bacterial cellulose is a biopolymer that is very similar to the fibre found in plants. The only difference is that bacterial cellulose is much purer and is made of randomly criss-crossed fibres compared with the regular ‘grain’ of plant cellulose. Paper made from bacterial cellulose is much smoother than normal paper and is currently used in ultra-high end speakers to produce cleaner sound.

Bacterial cellulose is not only physically strong, but it is biocompatible meaning it can be used in all sorts of clinical applications. Flat sheets of bacterial cellulose are already used in some forms of skin graft therapy and with JuicyPrint’s ability to print 3d structures, it will be possible to create effective tissue scaffolds for tissue engineering applications such as the growing of replacement organs.

How does it work?

The heart of JuicyPrint is our genetically engineered strain of the cellulose producing bacteria Gluconacetobacter hansenii (G. hansenii). G. hansenii (sometimes referred to as Acetobacter) is normally found growing in vinegar and is used in China to make a fermented tea called kombucha. G. hansenii can use lots of different liquids, such as fruit juice and beer brewing waste, as a food source, so almost anyone can grow them!

We are planning to insert genes that will let us switch on or switch off the cellulose production of the bacteria using light. Naturally occuring G. hansenii will produce a cellulose ‘pancake’ along the surface of the liquid nutrients they are grown in. But when a pattern of light is shined on the surface of a liquid culture of our engineered strain, only the bacteria in the dark patches will make cellulose so we can make the cellulose pancake any shape we want.

We can then push the patterned layer of cellulose below the surface and project a new pattern of light onto the culture. If we repeat this process a three dimensional structure will be built up out of the numerous patterned layers.