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Commit 498763de authored by carasj's avatar carasj
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achieve, attributions fixes

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<!--iGEM SPECIAL PRIZES-->
<h2 id="section-4">iGEM Special Prizes</h2>
<h3><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/education>Best Education</a></h3>
<!-- Carousel Best Education-->
<h3><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/software> Award for Best Software Tool</a></h3>
<img src="https://static.igem.wiki/teams/4188/wiki/wiki-images/teamfoto-software-award.jpg" style="width: 45%; float: right; margin-left: 30px; margin-top: 5px; margin-bottom: 10px;">
<p> &#10003; We developed a <b>user-friendly command line tool</b> that comprises flux scanning based on enforced
objective flux (FSEOF) for any metabolite of interest in a genome-scale metabolic model (GSMM). This software
identifies non-obvious genetic engineering targets for amplification that affect a metabolite of interest within a
timeframe of a few hours. With the descriptions and links to the code, we provide this tool for future use for
other iGEM teams.</p>
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</div>
<hr>
<div class="row mt-4 gy-3">
<div class="col-sm-12">
<h3><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/education>Nominated for Best Education</a></h3>
<!-- Carousel Nomination for Best Education-->
<div id="sp_be" class="carousel slide carousel-shape-outside" data-bs-ride="carousel"
style="width: 45%; float: right; margin-left: 30px; margin-top: 5px; margin-bottom: 10px;">
<!-- The slideshow/carousel -->
<div class="carousel-inner">
<div class="carousel-item active">
<!--Best Education-->
<!--Nomination for Best Education-->
<img src="https://static.igem.wiki/teams/4188/wiki/achievement-pictures/special-education-1.png" class="d-block w-100">
</div>
<div class="carousel-item">
<!--Best Education-->
<!--Nomination for Best Education-->
<img src="https://static.igem.wiki/teams/4188/wiki/achievement-pictures/special-education-2.png" class="d-block w-100">
</div>
</div>
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<h3><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/model>Best Model</a></h3>
<p> &#10003; We used <b>two models</b> to support and simplify our design and development of MonChassis. This assisted us to
identify engineering targets for our metabolic engineering approaches and investigate the growth media
composition. Our contributed models and descriptions in our deliverables will help future iGEM teams to make use of
this model and apply it to a vast space of application within metabolic engineering.</p>
<!--Nomination for Best Part Collection-->
<h3><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/part-collection#section-1> Nominated for Best Part
Collection</a></h3>
<p> &#10003; We provide RFC1000-compatible level 2 yeast shuttle vectors. Those have a shared design with the
RFC1000-compatible level 1 yeast shuttle vectors from iGEM Team TU Dresden. Using these shuttle vectors, an easy
introduction of all yeast-specific selection markers is possible. Moreover, they are compatible with the parts
from the Open Yeast Collection.</p>
</div>
</div>
......@@ -639,67 +655,34 @@
<div class="row mt-4 gy-3">
<div class="col-sm-12">
<h3><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/software>Best Software Tool</a></h3>
<p> &#10003; We developed a <b>user-friendly command line tool</b> that comprises flux scanning based on enforced
objective flux (FSEOF) for any metabolite of interest in a genome-scale metabolic model (GSMM). This software
identifies non-obvious genetic engineering targets for amplification that affect a metabolite of interest within a
timeframe of a few hours. With the descriptions and links to the code, we provide this tool for future use for
other iGEM teams.</p>
<!--Nomination for Best Biomanufacturing-->
<h3> Nominated for Best Biomanufacturing</h3>
</div>
</div>
<hr class="divider-big">
<hr>
<div class="row mt-4 gy-3">
<div class="col-sm-12">
<h3><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/parts>Best Part</a></h3>
<!-- Carousel Best Part-->
<div id="sp_bst" class="carousel slide carousel-shape-outside" data-bs-ride="carousel"
style="width: 45%; float: right; margin-left: 30px; margin-top: 5px; margin-bottom: 10px;">
<!-- The slideshow/carousel -->
<div class="carousel-inner">
<div class="carousel-item active">
<!--Best Part-->
<img src="https://static.igem.wiki/teams/4188/wiki/achievement-pictures/special-part-1.png" class="d-block w-100">
</div>
<div class="carousel-item">
<!--Best Part-->
<img src="https://static.igem.wiki/teams/4188/wiki/achievement-pictures/special-part-2.png" class="d-block w-100">
</div>
<div class="carousel-item">
<!--Best Part-->
<img src="https://static.igem.wiki/teams/4188/wiki/achievement-pictures/special-part-3.png" class="d-block w-100">
</div>
</div>
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<button class="carousel-control-prev" type="button" data-bs-target="#sp_bst" data-bs-slide="prev">
<span class="carousel-control-prev-icon"></span>
</button>
<button class="carousel-control-next" type="button" data-bs-target="#sp_bst" data-bs-slide="next">
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<p> &#10003; We provide a new <i>pSB3CY</i>_shuttle vector backbone with aeBlue for <i>Saccharomyces cerevisiae</i> [<a class="link-dark" href="http://parts.igem.org/Part:BBa_K4188001">BBa_K4188001</a>]</p>
<p> &#10003; We successfully designed, built, and tested a shuttle vector for S. cerevisiae transformations containing the 2µ ori and the chromoprotein aeBlue expression cassette. The latter is flanked by BsmBI restriction sites for easy introduction of a selection marker. Moreover, the shuttle vector includes the chromoprotein mRFP1 expression cassette between SapI restriction sites for insertion of a multi-transcription unit expressible in yeast.</br> Strains transformed with the newly designed level 2 shuttle vector can thus be selected by color. While the initial vector shows a purple color, successful transformants turn red if a selection marker is added via Golden Gate Assembly. Furthermore, the insertion of a successful Golden Gate Assembly with a multi-transcription unit into the site of the red chromoprotein (mRFP1) gene the vector shows blue staining of the colonies. If both chromoproteins are exchanged, the transformants become white and the vector can be used for transformation of S. cerevisiae after plasmid extraction.</p>
<!--Nomination for Best Wiki-->
<h3> Nominated for Best Wiki</h3>
</div>
</div>
<hr class="divider-big">
<hr>
<div class="row mt-4 gy-3">
<div class="col-sm-12">
<!--Best Part Collection-->
<h2><a class="link-dark" href=https://2022.igem.wiki/wwu-muenster/part-collection#section-1>Best Part
Collection</a></h2>
<p> &#10003; We provide RFC1000-compatible level 2 yeast shuttle vectors. Those have a shared design with the
RFC1000-compatible level 1 yeast shuttle vectors from iGEM Team TU Dresden. Using these shuttle vectors, an easy
introduction of all yeast-specific selection markers is possible. Moreover, they are compatible with the parts
from the Open Yeast Collection.</p>
<!--Nomination for Best Presentation-->
<h3> Nominated for Best Presentation</h3>
</div>
</div>
<hr><br>
<img src="https://static.igem.wiki/teams/4188/wiki/wiki-images/teamfoto-dach-grand-jamboree.jpg" style="width:100%">
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<p class="card-text">
<ul>
<li>Sponsoring</li>
<li>Education & communication – focus: public relation, bioethics</li>
<li>Group coordinator education & communication – focus: bioethics, public relation</li>
</ul>
</p>
</div>
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<li>Lab group <i><nobr>S. cerevisiae</nobr></i> peroxisome</li>
<li>Group coordinator human practices</li>
<li>Social media</li>
<li>Modeling</li>
</ul>
</p>
</div>
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