Difference between revisions of "Team:CCU Taiwan/Safety"

 
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                             <a href="https://2018.igem.org/Team:CCU_Taiwan/Team"><li class="list" id="home1">Team</li></a>
 
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<a href="https://2018.igem.org/Team:CCU_Taiwan/Achievements"><li class="list" id="home5">Achievements</li></a>
 
                         </ul>
 
                         </ul>
 
                     </li>
 
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<a href="https://2018.igem.org/Team:CCU_Taiwan/Results"><li class="list" id="project3">Results</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Results"><li class="list" id="project3">Results</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Demonstrate"><li class="list" id="project4">Demonstration</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Demonstrate"><li class="list" id="project4">Demonstration</li></a>
<a href="https://2018.igem.org/Team:CCU_Taiwan/InterLab "><li class="list" id="project5">InterLab</li></a>
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<a href="https://2018.igem.org/Team:CCU_Taiwan/InterLab"><li class="list" id="project5">InterLab</li></a>
 
</ul>
 
</ul>
 
</li>
 
</li>
 
                     <li class="title" style="cursor:pointer;" id="Parts"><img class="img_title" src="https://static.igem.org/mediawiki/2018/1/17/T--CCU_Taiwan--part.png"></img><a>Parts</a>
 
                     <li class="title" style="cursor:pointer;" id="Parts"><img class="img_title" src="https://static.igem.org/mediawiki/2018/1/17/T--CCU_Taiwan--part.png"></img><a>Parts</a>
 
                         <ul class="sub" id="sub_parts" style="cursor:default;">
 
                         <ul class="sub" id="sub_parts" style="cursor:default;">
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<a href="https://2018.igem.org/Team:CCU_Taiwan/Parts"><li class="list" id="parts1">Overview</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Basic_Part"><li class="list" id="parts1">Basic Part</li></a>
 
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<a href="https://2018.igem.org/Team:CCU_Taiwan/Improve"><li class="list" id="parts3">Improved Part</li></a>
 
 
                         </ul>
 
                         </ul>
 
                     </li>
 
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                         <ul class="sub" id="sub_modeling" style="cursor:default;">
 
                         <ul class="sub" id="sub_modeling" style="cursor:default;">
 
                             <a href="https://2018.igem.org/Team:CCU_Taiwan/Model"><li class="list" id="model1">Overview</li></a>
 
                             <a href="https://2018.igem.org/Team:CCU_Taiwan/Model"><li class="list" id="model1">Overview</li></a>
                             <a href="https://2018.igem.org/Team:CCU_Taiwan/Binding"><li class="list" id="model2">Binding</li></a>
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                             <a href="https://2018.igem.org/Team:CCU_Taiwan/Binding"><li class="list" id="model2">Binding Model</li></a>
<a href="https://2018.igem.org/Team:CCU_Taiwan/Polymer"><li class="list" id="model3">Polymer</li></a>
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<a href="https://2018.igem.org/Team:CCU_Taiwan/Polymer"><li class="list" id="model3">Polymer Model</li></a>
 
                         </ul>
 
                         </ul>
 
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    <li class="title" style="cursor:pointer;" id="Human_Practice"><img class="img_title" src="https://static.igem.org/mediawiki/2018/9/96/T--CCU_Taiwan--humanpractice.png"></img><a>HP</a>
 
    <li class="title" style="cursor:pointer;" id="Human_Practice"><img class="img_title" src="https://static.igem.org/mediawiki/2018/9/96/T--CCU_Taiwan--humanpractice.png"></img><a>HP</a>
 
                         <ul class="sub" id="sub_human_practice" style="cursor:default;">
 
                         <ul class="sub" id="sub_human_practice" style="cursor:default;">
                             <a href="https://2018.igem.org/Team:CCU_Taiwan/Human_Practices"><li class="list" id="human_practice1">Overview</li></a>
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                             <a href="https://2018.igem.org/Team:CCU_Taiwan/Human_Practices"><li class="list" id="human_practice1">Human Practice</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Public_Engagement"><li class="list" id="human_practice2">Public Engagement</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Public_Engagement"><li class="list" id="human_practice2">Public Engagement</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Entrepreneurship"><li class="list" id="human_practice3">Entrepreneurship</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/Entrepreneurship"><li class="list" id="human_practice3">Entrepreneurship</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/engaging_experts"><li class="list" id="human_practice4">Engaging Experts</li></a>
 
<a href="https://2018.igem.org/Team:CCU_Taiwan/engaging_experts"><li class="list" id="human_practice4">Engaging Experts</li></a>
<a href="https://2018.igem.org/Team:CCU_Taiwan/Intergrate"><li class="list" id="human_practice5">Intergrated HP</li></a>
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<a href="https://2018.igem.org/Team:CCU_Taiwan/Integrate"><li class="list" id="human_practice5">Integrated HP</li></a>
 
                         </ul>
 
                         </ul>
 
                     </li>
 
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             </div>
 
             </div>
 
         </nav>
 
         </nav>
 
  
 
     </header>
 
     </header>
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<div class="indicator">
 +
 +
<div class="pointerDrylab" id="1"><a href="#ca1">Filtering system</a></div>
 +
<div class="pointerDrylab" id="2"><a href="#ca2">Heating system</a></div>
 +
 +
</div>
  
 
<div class="backgroundDrylab">
 
<div class="backgroundDrylab">
<div class="photoSafety"></div>
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<div class="photoSafety"><h1 class="bigtitle">SAFETY<h1></div>
 
<div class="content">
 
<div class="content">
<p class="first">Safety</p><br><br>
+
<br><br>
<p class="description">&emsp;&emsp;Genetically modified organisms escaping from lab is a serious problem since it will bring unpredictable impacts to our ecosystem. In our part design and production line, we were very conscious of biosafety. The yeast will pass the following process to achieve complete destruction. We also dealt cautiously with waste produced from the experiment and participated in safety training to ensure everyone conducting experiments had a minimal probability to cause biohazard pollution.
+
<p class="description">&emsp;&emsp;The escaping of genetically modified organisms from labs is a serious problem since it will bring up unpredictable impacts to our ecosystem. We take biosafety very seriously when we design every parts of our experiment and the design of our production line.
 +
Our design of our production line insure that there's no genetically modified yeasts (also non-genetically modified yeasts) could survived and pass the whole production line and leak into the environment or residue on our products.
 +
We also dealt cautiously with wastes produced from the experiment and participated in safety training, to minimum the chance of causing biohazard pollution, or simply hurt ourselves.
 
</p>
 
</p>
<p class="second">Filtering system</p>
+
<p class="first" id="ca1">Filtering system</p>
<p class="description">&emsp;&emsp;The average size of the P. pastoris used is about 4–6 μm [1], and the filter we used is 33 kDa, which is equivalent to the size of tens of nanometers [2], more than sufficient to trap all the yeast.
+
<p class="description">&emsp;&emsp;The average size of the <I>P. pastoris</I> is about 4–6 μm (Gmeiner, C. et al. 2015), we use the MCE filter to separate the yeasts from leaking out the fermentation tank.
 
</p>
 
</p>
<p class="second">Heating system</p>
+
<p class="first" id="ca2">Heating system</p>
<p class="description">&emsp;&emsp;According to the literature [3], heating at 70 °C for 30 minutes is sufficient to kill the cells. We used a temperature of 110 ° C for 10 minutes to kill any cells that might pass through the filter.
+
<p class="description">&emsp;&emsp;According to the literature (Martínez, D. et al. 2015), heating at 70 °C for 1 day or incubate at 30 °C for 48 hr, is sufficient to kill all the yeasts.
 +
The minimum operating temperature of extrusion granulation will be over 110 °C. Therefore, no yeast could survived in the production line.
 
</p>
 
</p>
<p class="description">Following were our heating test:</p>
+
<p class="description">Following are our heating tests:</p>
<p class="description">Figure 1. P. pastoris heated at 30 °C for 30 minutes</p>
+
                <div id="Safety1" class="polaroid" style="display:inline-block">
<p class="description">Figure 2. P. pastoris heated at 50 °C for 30 minutes</p>
+
                  <img src="https://static.igem.org/mediawiki/2018/e/e8/T--CCU_Taiwan--CCUsafety.jpg" width="100%">
<p class="description">Figure 3. P. pastoris heated at 70 °C for 30 minutes</p>
+
                  <div class="container">
<p class="description">&emsp;&emsp;We found that our P. pastoris not survival after were heated at 50 °C for 30 minutes. Thus, our production line heat process would kill P. pastoris passing through the filter.</p>
+
                    <p>Figure1: <I>P. pastoris</I> yeast heated at 30 °C for 1 day , and incubated at 30 °C for 48 hr.<br>(left: 0.005, right: 0.05)</p>
+
                  </div>
+
                </div>
+
                <div id="Safety2" class="polaroid" style="display:inline-block">
+
                  <img src="https://static.igem.org/mediawiki/2018/4/4c/T--CCU_Taiwan--safety2.png" width="100%">
 +
                  <div class="container">
 +
                    <p>Figure2: <I>P. pastoris</I> yeast heated at 50 °C for 1 day , and incubated at 30 °C for 48 hr.</p>
 +
                  </div>
 +
                </div>
 +
                <div id="Safety3" class="polaroid" style="display:inline-block">
 +
                  <img src="https://static.igem.org/mediawiki/2018/1/1e/T--CCU_Taiwan--safety3.png" width="100%">
 +
                  <div class="container">
 +
                    <p>Figure3: <I>P. pastoris</I> yeast heated at 70 °C for 1 day , and incubate at 30 °C for 48 hr.</p>
 +
                  </div>
 +
                </div><br><br>
 +
<p class="description">&emsp;&emsp;We found that our <I>P. pastoris</I> diden't survive after were heated at 50 °C for 30 minutes. Which proof that the heat our production line generated could kill <I>P. pastoris</I> which pass the filter.</p>
 
 
 +
<br>
 +
<p class="second"><br>Reference</p>
 +
<p class="description">
 +
Gmeiner, C., Saadati, A., Maresch, D., Krasteva, S., Frank, M., Altmann, F., … Spadiut, O. (2015). Development of a fed-batch process for a recombinant <I>Pichia pastoris</I> Δoch1 strain expressing a plant peroxidase. Microbial Cell Factories, 14(1). doi:10.1186/s12934-014-0183-3<br>
 +
<br>Bacher, G., Szymanski, W. W., Kaufman, S. L., Zöllner, P., Blaas, D., & Allmaier, G. (2001). Charge-reduced nano electrospray ionization combined with differential mobility analysis of peptides, proteins, glycoproteins, noncovalent protein complexes and viruses. Journal of Mass Spectrometry, 36(9), 1038–1052.doi:10.1002/jms.208<br>
 +
<br>3. Martínez, D., Menéndez, C., Echemendia, F. M., Hernández, L., Sobrino, A., & Trujillo, L. E. (2015). Kinetics of sucrose hydrolysis by immobilized recombinant <I>Pichia pastoris</I> cells in a batch reactors. J Microb Biochem Technol, 7, 294-6.<br>
 
 
<p class="second"><br><br>Reference</p>
 
<p class="description"><ol>
 
<li>1. Gmeiner, C., Saadati, A., Maresch, D., Krasteva, S., Frank, M., Altmann, F., … Spadiut, O. (2015). Development of a fed-batch process for a recombinant Pichia pastoris Δoch1 strain expressing a plant peroxidase. Microbial Cell Factories, 14(1). <br>doi:10.1186/s12934-014-0183-3</li>
 
<li>Bacher, G., Szymanski, W. W., Kaufman, S. L., Zöllner, P., Blaas, D., & Allmaier, G. (2001). Charge-reduced nano electrospray ionization combined with differential mobility analysis of peptides, proteins, glycoproteins, noncovalent protein complexes and viruses.<br> Journal of Mass Spectrometry, 36(9), 1038–1052. <br>doi:10.1002/jms.208</li>
 
<li>3. Martínez, D., Menéndez, C., Echemendia, F. M., Hernández, L., Sobrino, A., & Trujillo, L. E. (2015). Kinetics of sucrose hydrolysis by immobilized recombinant Pichia pastoris cells in a batch reactors. J Microb Biochem Technol, 7, 294-6.</li>
 
</ol>
 
 
</p>
 
</p>
 
<br><br><br>
 
<br><br><br>

Latest revision as of 08:50, 1 December 2018

SAFETY



  The escaping of genetically modified organisms from labs is a serious problem since it will bring up unpredictable impacts to our ecosystem. We take biosafety very seriously when we design every parts of our experiment and the design of our production line. Our design of our production line insure that there's no genetically modified yeasts (also non-genetically modified yeasts) could survived and pass the whole production line and leak into the environment or residue on our products. We also dealt cautiously with wastes produced from the experiment and participated in safety training, to minimum the chance of causing biohazard pollution, or simply hurt ourselves.

Filtering system

  The average size of the P. pastoris is about 4–6 μm (Gmeiner, C. et al. 2015), we use the MCE filter to separate the yeasts from leaking out the fermentation tank.

Heating system

  According to the literature (Martínez, D. et al. 2015), heating at 70 °C for 1 day or incubate at 30 °C for 48 hr, is sufficient to kill all the yeasts. The minimum operating temperature of extrusion granulation will be over 110 °C. Therefore, no yeast could survived in the production line.

Following are our heating tests:

Figure1: P. pastoris yeast heated at 30 °C for 1 day , and incubated at 30 °C for 48 hr.
(left: 0.005, right: 0.05)

Figure2: P. pastoris yeast heated at 50 °C for 1 day , and incubated at 30 °C for 48 hr.

Figure3: P. pastoris yeast heated at 70 °C for 1 day , and incubate at 30 °C for 48 hr.



  We found that our P. pastoris diden't survive after were heated at 50 °C for 30 minutes. Which proof that the heat our production line generated could kill P. pastoris which pass the filter.



Reference

Gmeiner, C., Saadati, A., Maresch, D., Krasteva, S., Frank, M., Altmann, F., … Spadiut, O. (2015). Development of a fed-batch process for a recombinant Pichia pastoris Δoch1 strain expressing a plant peroxidase. Microbial Cell Factories, 14(1). doi:10.1186/s12934-014-0183-3

Bacher, G., Szymanski, W. W., Kaufman, S. L., Zöllner, P., Blaas, D., & Allmaier, G. (2001). Charge-reduced nano electrospray ionization combined with differential mobility analysis of peptides, proteins, glycoproteins, noncovalent protein complexes and viruses. Journal of Mass Spectrometry, 36(9), 1038–1052.doi:10.1002/jms.208

3. Martínez, D., Menéndez, C., Echemendia, F. M., Hernández, L., Sobrino, A., & Trujillo, L. E. (2015). Kinetics of sucrose hydrolysis by immobilized recombinant Pichia pastoris cells in a batch reactors. J Microb Biochem Technol, 7, 294-6.