Difference between revisions of "Team:San Andres/Parts"
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<img style="width: 962px; height: 325px;" | <img style="width: 962px; height: 325px;" | ||
src="https://static.igem.org/mediawiki/2015/thumb/8/8b/Gluten-s-Job.jpeg/800px-Gluten-s-Job.jpeg" | src="https://static.igem.org/mediawiki/2015/thumb/8/8b/Gluten-s-Job.jpeg/800px-Gluten-s-Job.jpeg" | ||
− | alt="File:Gluten-s-Job.jpeg"> | + | alt="File:Gluten-s-Job.jpeg" /> |
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-webkit-transform-style: preserve-3d; | -webkit-transform-style: preserve-3d; | ||
} | } | ||
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<table style="width: 968px; height: 34px;" | <table style="width: 968px; height: 34px;" | ||
class="gwd-table-nb4m editable"> | class="gwd-table-nb4m editable"> | ||
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<div class="gwd-div-2ed9"></div> | <div class="gwd-div-2ed9"></div> | ||
<div class="gwd-div-7xzo gwd-a-1thu"> | <div class="gwd-div-7xzo gwd-a-1thu"> | ||
− | <h1>Parts </h1> | + | <h1 style="font-family: Algerian;"><big>Parts </big></h1> |
− | <div style="text-align: justify;"><big>Throughout | + | <div style="text-align: justify; font-family: Cambria;"><big>Throughout |
the project we started to learn the fundamental | the project we started to learn the fundamental | ||
principles of synthetic biology to get to work on our plasmid with | principles of synthetic biology to get to work on our plasmid with | ||
which we want to see gluten degradation via the enzyme Kumamax. For | which we want to see gluten degradation via the enzyme Kumamax. For | ||
this we going to insert in an e. coli the parts (Biobricks) needed to | this we going to insert in an e. coli the parts (Biobricks) needed to | ||
− | make our future bacteria can degrade gluten. The parts are:</big><br> | + | make our future bacteria can degrade gluten. The parts are:</big><br /> |
</div> | </div> | ||
− | <ul> | + | <ul style="font-family: Cambria;"> |
− | <li style="text-align: justify;"><big | + | <li style="text-align: justify;"><big><strong |
− | + | ||
style="font-weight: bold;">Promoter | style="font-weight: bold;">Promoter | ||
<a href="http://parts.igem.org/Part:BBa_J23119">(BBa_J23119</a></strong><a | <a href="http://parts.igem.org/Part:BBa_J23119">(BBa_J23119</a></strong><a | ||
href="http://parts.igem.org/Part:BBa_J23119"><span | href="http://parts.igem.org/Part:BBa_J23119"><span | ||
style="font-weight: bold;">)</span></a>: | style="font-weight: bold;">)</span></a>: | ||
− | + | Constitutive | |
promoter (which works permanently) that is give in the relative | promoter (which works permanently) that is give in the relative | ||
fluorescence of these plasmids in the TG1 strain grown in LB medium.</big> | fluorescence of these plasmids in the TG1 strain grown in LB medium.</big> | ||
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href="http://parts.igem.org/Part:pSB1C3">pSB1C3</a></span></strong></big> | href="http://parts.igem.org/Part:pSB1C3">pSB1C3</a></span></strong></big> | ||
</li> | </li> | ||
− | <li style="text-align: justify;"><big><strong> | + | <li style="text-align: justify;"><big><strong>Coding |
− | + | Region: | |
− | KumaMax <a href="http://parts.igem.org/Part:BBa_K590087">(BBa_K590087)</a>: | + | KumaMax <a href="http://parts.igem.org/Part:BBa_K590087">(BBa_K590087)</a>:</strong> |
It | It | ||
degrades gluten, | degrades gluten, | ||
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2011.</a></big> | 2011.</a></big> | ||
</li> | </li> | ||
− | <li style="text-align: justify;"><big><strong | + | <li style="text-align: justify;"><big><strong>Reporter: |
− | + | RFP | |
− | <a href="http://parts.igem.org/Part:BBa_J04450">(BBa_J04450)</a>: | + | <a href="http://parts.igem.org/Part:BBa_J04450">(BBa_J04450)</a>:</strong> |
− | + | Red fluorescence | |
protein.</big> | protein.</big> | ||
</li> | </li> | ||
− | <li style="text-align: justify;"><big | + | <li style="text-align: justify;"><big><strong>Terminator |
− | + | ||
<a href="http://parts.igem.org/Part:BBa_B0015">(BBa_B0015)</a>:</strong> | <a href="http://parts.igem.org/Part:BBa_B0015">(BBa_B0015)</a>:</strong> | ||
− | + | Dual terminator consisting of | |
the B0010 and B0012 parties. It serves to give greater efficiency in | the B0010 and B0012 parties. It serves to give greater efficiency in | ||
transcription</big>.</li> | transcription</big>.</li> | ||
</ul> | </ul> | ||
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<img alt="File:Parts.jpg" | <img alt="File:Parts.jpg" | ||
src="https://static.igem.org/mediawiki/2015/e/e8/Parts.jpg" | src="https://static.igem.org/mediawiki/2015/e/e8/Parts.jpg" | ||
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</big></div> | </big></div> | ||
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+ | href="https://2015.igem.org/Main_Page" | ||
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href="https://igem.org/Team_List?year=2015" | href="https://igem.org/Team_List?year=2015" | ||
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src="https://static.igem.org/mediawiki/2015/thumb/8/85/Logo_Definitvo.png/654px-Logo_Definitvo.png" | src="https://static.igem.org/mediawiki/2015/thumb/8/85/Logo_Definitvo.png/654px-Logo_Definitvo.png" | ||
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</html> | </html> |
Revision as of 01:49, 15 September 2015
Home | Team | Project | Parts | Modeling | Results |
Notebook | Human Practices | Future Projections | Attributions | Collaborations |
Parts
Throughout
the project we started to learn the fundamental
principles of synthetic biology to get to work on our plasmid with
which we want to see gluten degradation via the enzyme Kumamax. For
this we going to insert in an e. coli the parts (Biobricks) needed to
make our future bacteria can degrade gluten. The parts are:
- Promoter (BBa_J23119): Constitutive promoter (which works permanently) that is give in the relative fluorescence of these plasmids in the TG1 strain grown in LB medium.
- RBS (BBa_K1084103): Synthetic RBS with uplifting sequence.
- Vector: pSB1C3
- Coding Region: KumaMax (BBa_K590087): It degrades gluten, celiac disease leading cause. Enzyme generated by rational mutation for the active site of it. It was created by the team IGEM Washington 2011.
- Reporter: RFP (BBa_J04450): Red fluorescence protein.
- Terminator (BBa_B0015): Dual terminator consisting of the B0010 and B0012 parties. It serves to give greater efficiency in transcription.