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</div> | </div> | ||
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<div class="column full_size general_p"> | <div class="column full_size general_p"> | ||
<h2>Aachen</h2> | <h2>Aachen</h2> | ||
− | |||
− | <div class="team_information_wrapper | + | <p><b>Institution: </b>Aachen University</p> |
+ | |||
+ | <div class="team_information_wrapper"> | ||
<p> | <p> | ||
<b> | <b> | ||
<svg enable-background="new 0 0 250 250" version="1.1" viewBox="0 0 250 250" xml:space="preserve" height="20px"> | <svg enable-background="new 0 0 250 250" version="1.1" viewBox="0 0 250 250" xml:space="preserve" height="20px"> | ||
− | <style type="text/css"> .st0{fill:#085156;} </style> | + | <style type="text/css"> .st0{fill:#085156; margin-bottom:-5px} </style> |
<circle class="st0" cx="125" cy="104.1" r="17.9"/> | <circle class="st0" cx="125" cy="104.1" r="17.9"/> | ||
<path class="st0" d="m125 33c-50.8 0-92 41.2-92 92s41.2 92 92 92 92-41.2 92-92-41.2-92-92-92zm31.6 98l-31.6 53.7-31.6-53.7c-3.7-6.4-7.2-17.3-7.2-25.4 0-22.2 17.4-40.3 38.8-40.3s38.8 18 38.8 40.3c0 8-3.5 19-7.2 25.4z"/></svg> | <path class="st0" d="m125 33c-50.8 0-92 41.2-92 92s41.2 92 92 92 92-41.2 92-92-41.2-92-92-92zm31.6 98l-31.6 53.7-31.6-53.7c-3.7-6.4-7.2-17.3-7.2-25.4 0-22.2 17.4-40.3 38.8-40.3s38.8 18 38.8 40.3c0 8-3.5 19-7.2 25.4z"/></svg> | ||
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<b>Region: </b>Europe<br> | <b>Region: </b>Europe<br> | ||
<b>Section: </b>Overgrad<br> | <b>Section: </b>Overgrad<br> | ||
− | <b>Track: </b>Environment</p> | + | <b>Track: </b>Environment |
+ | |||
+ | </p> | ||
</div> | </div> | ||
− | <div class="team_information_wrapper | + | <div class="team_information_wrapper"> |
+ | <p><b>Parts: </b><a href="http://parts.igem.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2019&group=Aachen">parts/Team:Aachen</a><br><b>Wiki: </b> <a href="https://2019.igem.org/Team:Aachen">2019/Team:Aachen</a><br><b>Poster: </b>Zone 3 - 260<br><b>Presentation: </b>Saturday - Room Ballroom A - 11:30 AM</p> | ||
+ | |||
+ | </div> | ||
+ | |||
+ | <div class="team_information_wrapper"> | ||
+ | <p><b>Medal: </b>Gold<br> | ||
+ | <b>Nominations: </b>Best Environment Project<br> | ||
+ | <b>Awards: </b>- | ||
+ | </p> | ||
+ | </div> | ||
+ | |||
− | |||
<div class="clear extra_space"></div> | <div class="clear extra_space"></div> | ||
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<h4>Plastractor - extracting microplastics from fluids via magnets</h4> | <h4>Plastractor - extracting microplastics from fluids via magnets</h4> | ||
+ | |||
<p>Nowadays the problem of microplastics in fluids like drinkable water is a huge topic with a lot of new publications and studies about the amount, types and risks of it for animals, environment and humans. The `Plastractor` is a device which shall extract microplastics from fluids easily via magnets. Therefore the bacterium Rhodospirillum rubrum `magneticum` was obtained. It is genetically modified to build magnetosomes; small magnetic and vesicle-like particles, with plastic binding peptides on its membrane. For modification we use E. coli BW29427 which transfers the needed plasmid to Rhodospirillum rubrum `magneticum` via conjugation. Two different plastic binding peptides are used, `Tachystatin A2` (TA2) and `liquid chromatography peak I` (LCI), fused with two different fluorescent proteins to enable the detection of the bound particles. Thus the device will be able to extract the plastics that are bound to magnetosomes and detect it by fluorescence.</p> | <p>Nowadays the problem of microplastics in fluids like drinkable water is a huge topic with a lot of new publications and studies about the amount, types and risks of it for animals, environment and humans. The `Plastractor` is a device which shall extract microplastics from fluids easily via magnets. Therefore the bacterium Rhodospirillum rubrum `magneticum` was obtained. It is genetically modified to build magnetosomes; small magnetic and vesicle-like particles, with plastic binding peptides on its membrane. For modification we use E. coli BW29427 which transfers the needed plasmid to Rhodospirillum rubrum `magneticum` via conjugation. Two different plastic binding peptides are used, `Tachystatin A2` (TA2) and `liquid chromatography peak I` (LCI), fused with two different fluorescent proteins to enable the detection of the bound particles. Thus the device will be able to extract the plastics that are bound to magnetosomes and detect it by fluorescence.</p> | ||
</div> | </div> |
Revision as of 19:38, 19 November 2019
HQ
This page contains the list of HQ pages and resources used in 2019.
HQ pages in 2019
Code wishlist
Here you can add classes or special requests for css/jquery you would like to have in 2019
- Different colors for the decoration class
- Code documentation for creating div with centered text -AES
2019 pending template update
Ana's to do list for 2019 code
- Add social media links to the bottom of the menu
- Fix nesting font sizes ol/ul
- Finish code documentation
Aachen
Institution: Aachen University
Location: Germany
Region: Europe
Section: Overgrad
Track: Environment
Parts: parts/Team:Aachen
Wiki: 2019/Team:Aachen
Poster: Zone 3 - 260
Presentation: Saturday - Room Ballroom A - 11:30 AM
Medal: Gold
Nominations: Best Environment Project
Awards: -
Plastractor - extracting microplastics from fluids via magnets
Nowadays the problem of microplastics in fluids like drinkable water is a huge topic with a lot of new publications and studies about the amount, types and risks of it for animals, environment and humans. The `Plastractor` is a device which shall extract microplastics from fluids easily via magnets. Therefore the bacterium Rhodospirillum rubrum `magneticum` was obtained. It is genetically modified to build magnetosomes; small magnetic and vesicle-like particles, with plastic binding peptides on its membrane. For modification we use E. coli BW29427 which transfers the needed plasmid to Rhodospirillum rubrum `magneticum` via conjugation. Two different plastic binding peptides are used, `Tachystatin A2` (TA2) and `liquid chromatography peak I` (LCI), fused with two different fluorescent proteins to enable the detection of the bound particles. Thus the device will be able to extract the plastics that are bound to magnetosomes and detect it by fluorescence.