Difference between revisions of "Team:Consort Alberta/Parts"

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{{Consort_Alberta}}
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<h2> Part Documentation</h2>
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<p>Each team will make new parts during iGEM and will submit them to the Registry of Standard Biological Parts. The iGEM software provides an easy way to present the parts your team has created. The <code>&lt;groupparts&gt;</code> tag (see below) will generate a table with all of the parts that your team adds to your team sandbox.</p>
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<link rel="stylesheet" type="text/css" href="https://2015.igem.org/Team:Consort_Alberta/css?action=raw&ctype=text/css" />
<p>Remember that the goal of proper part documentation is to describe and define a part, so that it can be used without needing to refer to the primary literature. Registry users in future years should be able to read your documentation and be able to use the part successfully. Also, you should provide proper references to acknowledge previous authors and to provide for users who wish to know more.</p>
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<h4>Note</h4>
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<div id="home_CON">
<p>Note that parts must be documented on the <a href="http://parts.igem.org/Main_Page"> Registry</a>. This page serves to <i>showcase</i> the parts you have made. Future teams and other users and are much more likely to find parts by looking in the Registry than by looking at your team wiki.</p>
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<a href="https://2015.igem.org/Team:Consort_Alberta"><img id="logo_CON" src="https://static.igem.org/mediawiki/2015/4/43/Consort_logo.png" alt="Logo and link to home page" /></a>
 
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<div id="navigation_CON">
 
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<ul>
<h4>Adding parts to the registry</h4>
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<li class="navitaion_right_border_CON"><a href="https://2015.igem.org/Team:Consort_Alberta">Home</a></li>
<p>You can add parts to the Registry at our <a href="http://parts.igem.org/Add_a_Part_to_the_Registry">Add a Part to the Registry</a> link.</p>
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<li class="navitaion_right_border_CON"><a href="https://2015.igem.org/Team:Consort_Alberta/project">Project</a>
<p>We encourage teams to start completing documentation for their parts on the Registry as soon as you have it available. The sooner you put up your parts, the better you will remember all the details about your parts. Remember, you don't need to send us the DNA sample before you create an entry for a part on the Registry. (However, you <b>do</b> need to send us the DNA sample before the Jamboree. If you don't send us a DNA sample of a part, that part will not be eligible for awards and medal criteria.)</p>
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<div class="navigation_expand_cell_CON">
 
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<li><a href="https://2015.igem.org/Team:Consort_Alberta/project">Parts</a></li>
<h4>What information do I need to start putting my parts on the Registry?</h4>
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<li><a href="https://2015.igem.org/Team:Consort_Alberta/project">Collaborations</a></li>
<p>The information needed to initially create a part on the Registry is:</p>
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                                                                                <li><a href="https://2015.igem.org/Team:Consort_Alberta/project">Design</a></li>
<ul>
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</ul>
<li>Part Name</li>
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</div>
<li>Part type</li>
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</li>
<li>Creator</li>
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<li class="navitaion_right_border_CON"><a href="https://2015.igem.org/Team:Consort_Alberta/team">Team</a></li>
<li>Sequence</li>
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<li class="navitaion_right_border_CON"><a href="https://2015.igem.org/Team:Consort_Alberta/humanpractices">Outreach</a>
<li>Short Description (60 characters on what the DNA does)</li>
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<div class="navigation_expand_cell_CON">
<li>Long Description (Longer description of what the DNA does)</li>
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<ul>
<li>Design considerations</li>
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<li><a href="https://2015.igem.org/Team:Consort_Alberta/humanpractices#practices">Outreach</a></li>
</ul>
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<li><a href="https://2015.igem.org/Team:Consort_Alberta/humanpractices#outreach">Practices</a></li>
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</ul>
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</div>
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</li>
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<li class="navitaion_right_border_CON"><a href="https://2015.igem.org/Team:Consort_Alberta/notebook">Notebook</a></li>
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<li class="navitaion_right_border_CON"><a href="https://2015.igem.org/Team:Consort_Alberta/safety">Safety</a></li>
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<li class="navitaion_right_border_CON"><a href="https://2015.igem.org/Team:Consort_Alberta/sponsors">Attributions</a></li>
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<li><a href="contact">Contact Us</a></li>
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</ul>
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<h1 class="left_heading_CON">ECOS</h1>
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<div class="heading_to_left_CON">
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<p>ECOS is a BioBrick designed to detect xylene. Xylene is a carcinogen in crude oil that is closely associated with two other aromatic hydrocarbons, benzene and toluene,that are the more dangerous compounds in crude oil. In Consort, Alberta, our economy is based almost entirely on agriculture and the oil industry. These two portions of the economy coexist side by side; oil wells are drilled on land adjacent to crops and cattle. This poses an issue if oil spills occur. While oil companies have strict regulations and protocols that they follow, it is always important that we increase our environmental stewardship. There is not a test currently that can check for contamination on site. There is little one can do after sending a sample to a lab and not receiving results back for weeks at a time. In order to properly monitor these sites, farmers and oil companies alike need the tools to do so. This is where we come it. ECOS will provide an on-site test that is cheap, efficient and easy. After talking to many community members we believe that our project could be used for semi-annual testing of sites, water monitoring and post spill monitoring.</p>
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<h1 class="left_heading_CON">Our Biobrick:</h1>
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<p>ECOS consists of the following parts:</p>
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<p>(Pic of sequence without reporter)</p>
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<p>
 
<p>
We encourage you to put up <em>much more</em> information as you gather it over the summer. If you have images, plots, characterization data and other information, please also put it up on the part page. </p>
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J23100 - which is a constituent promoter.<br />
 
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B0034 - the RBS for our XylR gene.<br />
 
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I723017 - the XylR coding region which encodes for the transcriptional regulator XylR protein.<br />
 
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B0015 - the double stop codon for this sequence.<br />
 
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I723020 - This is the Pu promoter.<br />
 
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B0030 - RBS.1 strong.<br />
 
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</p>
<h4>Inspiration</h4>
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<p>We have a created  a <a href="http://parts.igem.org/Well_Documented_Parts">collection of well documented parts</a> that can help you get started.</p>
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<p>We also attached the Reporter AmilCP in the backbone pCB1C3 to give us an output in correspondence to the level of xylene present.</p>
 
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<p> You can also take a look at how other teams have documented their parts in their wiki:</p>
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<p>(pic of whole sequence) </p>
<ul>
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<li><a href="https://2014.igem.org/Team:MIT/Parts"> 2014 MIT </a></li>
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<li><a href="https://2014.igem.org/Team:Heidelberg/Parts"> 2014 Heidelberg</a></li>
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<li><a href="https://2014.igem.org/Team:Tokyo_Tech/Parts">2014 Tokyo Tech</a></li>
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</ul>
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<h4>Part Table </h4>
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<groupparts>iGEM015 Example</groupparts>
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<h1 class="left_heading_CON">Our Prototypes</h1>
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<div class="heading_to_left_CON">
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<h2>Prototype 1:Animation</h2>
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<p>Alginate beads!  We were hoping we were going to be able to trap our E.coli containing ECOS in the matrix of alginate beads. Alginate is easy to manipulate, it is cheap, light and safe. It would also be extraordinarily simple to operate as you simply place the beads in the soil or water and wait. We did several trials with alginate; experimenting with different protocols to form the beads. Unfortunately the beads ended up being totally opaque. With our trials with ECOS, we had to spin the cells down to see the AmilCP. You could not detect a colour change when the cells were suspended in the LB. With this information, there is no way we would be able to tell if the protein was being produced or not in the alginate beads. We also looked into making beads out of agar. Agar is too porous though and would not be able to hold the bacteria within the matrix.</p>
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<p>(pic of both beads with labels)</p>
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<h2>Prototype 2: (Animation)</h2>
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<p>While this prototype is slightly more complicated, at this point we may have to sacrifice simplicity for something that will give us results. We designed this prototype so that it has a positive pressure source which creates a current for our xylene to travel from our sample, which is in a heated container so that the xylene is vaporized, to our ECOS container in which we bubble it through the E.coli culture to get results. This was a plausible idea, as it would require fairly non-expensive materials and could be maintained by the average business person.</p>
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<h2>Our Results</h2>
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<p>We were able to successfully create two parts. The first being just ECOS and the second having AmilCP attached. We did a lab on the part including AmilCP and did have positive results!</p>
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<p>(Photo’s with labeling guide attached)</p>
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<p>For more details please view our lab write up on the part!</p>
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<p>(LAB WRITE UP goes here… it’s referred to in the notebook a lot)</p>
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<h2>Our Future Plans</h2>
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<p>As AmilCP is hard to see, we plan to look into finding a different reporter which will be easier to work with. Protein Paintbox has many different and vibrant proteins that may work better with ECOS. We have also discussed improving our prototype to make it as efficient as possible. A “seek and destroy” idea has also been brought up. This would mean we could not only detect the oil but also break down the harmful carcinogens contained in it.</p>
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Revision as of 21:31, 16 September 2015

ECOS

ECOS is a BioBrick designed to detect xylene. Xylene is a carcinogen in crude oil that is closely associated with two other aromatic hydrocarbons, benzene and toluene,that are the more dangerous compounds in crude oil. In Consort, Alberta, our economy is based almost entirely on agriculture and the oil industry. These two portions of the economy coexist side by side; oil wells are drilled on land adjacent to crops and cattle. This poses an issue if oil spills occur. While oil companies have strict regulations and protocols that they follow, it is always important that we increase our environmental stewardship. There is not a test currently that can check for contamination on site. There is little one can do after sending a sample to a lab and not receiving results back for weeks at a time. In order to properly monitor these sites, farmers and oil companies alike need the tools to do so. This is where we come it. ECOS will provide an on-site test that is cheap, efficient and easy. After talking to many community members we believe that our project could be used for semi-annual testing of sites, water monitoring and post spill monitoring.

Our Biobrick:

ECOS consists of the following parts:

(Pic of sequence without reporter)

J23100 - which is a constituent promoter.
B0034 - the RBS for our XylR gene.
I723017 - the XylR coding region which encodes for the transcriptional regulator XylR protein.
B0015 - the double stop codon for this sequence.
I723020 - This is the Pu promoter.
B0030 - RBS.1 strong.

We also attached the Reporter AmilCP in the backbone pCB1C3 to give us an output in correspondence to the level of xylene present.

(pic of whole sequence)

Our Prototypes

Prototype 1:Animation

Alginate beads! We were hoping we were going to be able to trap our E.coli containing ECOS in the matrix of alginate beads. Alginate is easy to manipulate, it is cheap, light and safe. It would also be extraordinarily simple to operate as you simply place the beads in the soil or water and wait. We did several trials with alginate; experimenting with different protocols to form the beads. Unfortunately the beads ended up being totally opaque. With our trials with ECOS, we had to spin the cells down to see the AmilCP. You could not detect a colour change when the cells were suspended in the LB. With this information, there is no way we would be able to tell if the protein was being produced or not in the alginate beads. We also looked into making beads out of agar. Agar is too porous though and would not be able to hold the bacteria within the matrix.

(pic of both beads with labels)

Prototype 2: (Animation)

While this prototype is slightly more complicated, at this point we may have to sacrifice simplicity for something that will give us results. We designed this prototype so that it has a positive pressure source which creates a current for our xylene to travel from our sample, which is in a heated container so that the xylene is vaporized, to our ECOS container in which we bubble it through the E.coli culture to get results. This was a plausible idea, as it would require fairly non-expensive materials and could be maintained by the average business person.

Our Results

We were able to successfully create two parts. The first being just ECOS and the second having AmilCP attached. We did a lab on the part including AmilCP and did have positive results!

(Photo’s with labeling guide attached)

For more details please view our lab write up on the part!

(LAB WRITE UP goes here… it’s referred to in the notebook a lot)

Our Future Plans

As AmilCP is hard to see, we plan to look into finding a different reporter which will be easier to work with. Protein Paintbox has many different and vibrant proteins that may work better with ECOS. We have also discussed improving our prototype to make it as efficient as possible. A “seek and destroy” idea has also been brought up. This would mean we could not only detect the oil but also break down the harmful carcinogens contained in it.