Difference between revisions of "Team:CIEI-BJ"

 
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<img src="https://static.igem.org/mediawiki/2018/0/0b/T--CIEI-BJ--Team--Home--fig-top.jpg" style="width: 100%;border-radius: 10px;" />
 
<img src="https://static.igem.org/mediawiki/2018/0/0b/T--CIEI-BJ--Team--Home--fig-top.jpg" style="width: 100%;border-radius: 10px;" />
  
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<h2>A Yeast System</h2> for  
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<h2>Detection & Degradation</h2> of
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<h2>A flatoxin B1</h2>
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<div>A Yeast System <small>for</small></div>
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<div>Detection <small>&</small></div>
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<div>Degradation <small>of</small></div>
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<div>Aflatoxin B1</div>
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<div id="adjust-padder">
 
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<div class="first-level" style="font-size: 2.2em">A yeast system for detection and degradation of aflatoxin B1</div>
 
<div class="first-level" style="font-size: 2.2em">A yeast system for detection and degradation of aflatoxin B1</div>
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<p class="my-content" >Our project is inspired by the possible contamination of the carcinogenic aflatoxins (AFTs), in Pu?er, a Chinese traditional fermented tea. We aim to design a genetically engineered yeast system to detect and degrade its widely occurred species AFT-B1. Our system contains three modules-induction, detection and degradation. The induction module was designed based on an iGEM project in 2017 using two fragments of an antibody against AFT-B1. The detection module utilizes enhanced yellow fluorescent protein to indicate the presence of ATF-B1. In the degradation module, four candidate enzymes were incorporated individually and their activities were assessed. Both detection and degradation modules are triggered when AFT-B1 bridges the two antibody fragments. Our design not only provides a parallel detection and degradation in yeast with potential practical value for Pu?er Tea and other agricultural products, but also establishes a convenient screening system for identifying novel AFT-B1-degrading enzymes. </p>
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<p class="my-content" >Our project is inspired by the possible contamination of the carcinogenic aflatoxins (AFTs), in Pu'er, a Chinese traditional fermented tea. We aim to design a genetically engineered yeast system to detect and degrade its widely occurred species AFT-B1. Our system contains three modules-induction, detection and degradation. The induction module was designed based on an iGEM project in 2017 using two fragments of an antibody against AFT-B1. The detection module utilizes enhanced yellow fluorescent protein to indicate the presence of ATF-B1. In the degradation module, four candidate enzymes were incorporated individually and their activities were assessed. Both detection and degradation modules are triggered when AFT-B1 bridges the two antibody fragments. Our design not only provides a parallel detection and degradation in yeast with potential practical value for Pu'er Tea and other agricultural products, but also establishes a convenient screening system for identifying novel AFT-B1-degrading enzymes. </p>
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<div class="index-img-wrapper">
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    <div class="img-row">
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        <div class="img-item">
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            <div>
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                <img src="https://static.igem.org/mediawiki/2018/2/21/T--CIEI-BJ--Home--Index--fig2.jpg" alt="fig">
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            </div>
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            <div class="img-txt">
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                <a href="https://2018.igem.org/Team:CIEI-BJ/Background">Background</a>
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            </div>
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        </div>
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        <div class="img-item">
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            <div>
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                <img src="https://static.igem.org/mediawiki/2018/0/0c/T--CIEI-BJ--Home--Index--fig4.jpg" alt="fig">
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            </div>
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            <div class="img-txt">
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                <a href="https://2018.igem.org/Team:CIEI-BJ/Design">Design</a>
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            </div>
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        </div>
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        <div class="img-item">
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            <div>
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                <img src="https://static.igem.org/mediawiki/2018/e/eb/T--CIEI-BJ--Home--Index--fig5.jpg" alt="fig">
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            </div>
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            <div class="img-txt">
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                <a href="https://2018.igem.org/Team:CIEI-BJ/Results">Results</a>
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            </div>
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    <div class="img-row">
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        <div class="img-item">
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            <div>
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                <img src="https://static.igem.org/mediawiki/2018/2/2a/T--CIEI-BJ--Home--Index--fig3.jpg" alt="fig">
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            </div>
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            <div class="img-txt">
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                <a href="https://2018.igem.org/Team:CIEI-BJ/Human_Practices">HP</a>
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            </div>
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        </div>
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        <div class="img-item">
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            <div>
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                <img src="https://static.igem.org/mediawiki/2018/d/d3/T--CIEI-BJ--Home--Index--fig1.jpg" alt="fig">
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            </div>
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            <div class="img-txt">
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                <a href="https://2018.igem.org/Team:CIEI-BJ/Notebook">Notebook</a>
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            </div>
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        </div>
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        <div class="img-item">
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            <div>
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                <img src="https://static.igem.org/mediawiki/2018/5/56/T--CIEI-BJ--Home--Index--fig6.jpg" alt="fig">
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            </div>
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            <div class="img-txt">
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                <a href="https://2018.igem.org/Team:CIEI-BJ/Team">Team</a>
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            </div>
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        </div>
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    </div>
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</div>
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</div>
 
</div>
 
</div>
 
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Latest revision as of 16:24, 17 October 2018

Top

A Yeast System for
Detection &
Degradation of
Aflatoxin B1

A yeast system for detection and degradation of aflatoxin B1

Our project is inspired by the possible contamination of the carcinogenic aflatoxins (AFTs), in Pu'er, a Chinese traditional fermented tea. We aim to design a genetically engineered yeast system to detect and degrade its widely occurred species AFT-B1. Our system contains three modules-induction, detection and degradation. The induction module was designed based on an iGEM project in 2017 using two fragments of an antibody against AFT-B1. The detection module utilizes enhanced yellow fluorescent protein to indicate the presence of ATF-B1. In the degradation module, four candidate enzymes were incorporated individually and their activities were assessed. Both detection and degradation modules are triggered when AFT-B1 bridges the two antibody fragments. Our design not only provides a parallel detection and degradation in yeast with potential practical value for Pu'er Tea and other agricultural products, but also establishes a convenient screening system for identifying novel AFT-B1-degrading enzymes.

fig
Background
fig
Design
fig
Results
fig
HP
fig
Notebook
fig
Team