Difference between revisions of "Team:RDFZ-China/Demonstrate"

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{{RDFZ-China}}
 
{{RDFZ-China}}
 +
 
<html>
 
<html>
 +
<style>
 +
    body {
 +
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 +
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<div class="clear"></div>
+
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    #basic_description {
 +
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 +
        /*also eliminate any margin*/
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 +
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 +
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    #_footer p {
 +
        text-align: center;
 +
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<div class="column full_size">
+
    .description {
<h1>Demonstrate</h1>
+
        width: 1000px;
<h3>Gold Medal Criterion #4</h3>
+
        margin-left: auto;
 +
        margin-right: auto;
 +
        font-family: Avenir;
 +
        font-size: large;
 +
        padding-bottom: 30px;
 +
    }
  
<p>
+
    .description li, .description p {
Teams that can show their system working under real world conditions are usually good at impressing the judges in iGEM. To achieve gold medal criterion #4, convince the judges that your project works. There are many ways in which your project working could be demonstrated, so there is more than one way to meet this requirement. This gold medal criterion was introduced in 2016, so check our what 2016 teams did to achieve their gold medals!
+
        color: #404040;
</p>
+
    }
  
<p>
+
    .description h3 {
Please see the <a href="https://2018.igem.org/Judging/Medals">2018 Medals Page</a> for more information.
+
        font-family:'Avenir';
</p>
+
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 +
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 +
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 +
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 +
        font-family: Avenir !important;
 +
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</div>
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-->
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+
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+
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    <title>RDFZ-China</title>
+
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<style>
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.igem_2018_team_content,.igem_2018_team_content .igem_2018_team_column_wrapper{
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margin:auto;
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+
  
.igem_2018_team_menu.displaying_menu{
+
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display:none;
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.igem_2018_team_content .igem_2018_team_column_wrapper h3,
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.igem_2018_team_content .igem_2018_team_column_wrapper h1,
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color:pink;
 
text-shadow: 0px 0px 8px rgba(0, 0, 0,.2);
 
text-align: left
 
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p{
+
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+
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+
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+
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+
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+
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+
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+
  
/*CSS for Navibar*/
+
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+
  
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+
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+
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/* Next & previous buttons */
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+
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+
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+
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+
  
/* Position the "next button" to the right */
+
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+
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+
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+
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+
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+
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+
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+
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+
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+
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+
  
/* Caption text */
+
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+
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+
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+
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+
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+
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+
  
/* Number text (1/3 etc) */
+
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+
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+
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+
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+
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+
  
/* The dots/bullets/indicators */
+
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+
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+
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+
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+
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+
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+
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+
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+
  
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+
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+
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+
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/* Fading animation */
+
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+
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+
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+
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+
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+
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+
  
@-webkit-keyframes fade {
+
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  from {opacity: .4}
+
         padding-top: 50px;
  to {opacity: 1}
+
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}
+
 
+
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+
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+
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+
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+
 
+
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+
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+
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+
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+
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+
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+
 
+
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+
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+
 
+
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+
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+
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+
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+
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+
.footerimage3{
+
width:20%;
+
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+
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+
.inlabdiv {
+
margin-bottom: 2%;
+
margin-left: 2%;
+
}
+
.interlab{
+
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+
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+
        margin-left: 0%;
+
        margin-right: 0%;
+
        text-align: left;
+
}
+
header {
+
position: absolute;
+
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+
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+
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+
margin-top: 0;
+
height: 100px;
+
background-color: aliceblue;
+
right: 0px;
+
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+
}
+
 
+
#topicimg{
+
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+
        margin: auto;
+
position: relative;
+
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+
}
+
 
+
#footer ul{list-style: none;}
+
#footer li{display: block; margin: 0 1.2em;}
+
#footer img{float:left;}
+
#footer {
+
position: relative;
+
top: 1000px;
+
}
+
 
+
main {
+
        width:100%;
+
        margin:auto;
+
padding: 0px;
+
margin: 0px;
+
position: relative;
+
height: auto;
+
}
+
  
 +
    .reference {
 +
        width: 1000px;
 +
        margin-left: auto;
 +
        margin-right: auto;
 +
        font-family: Arial, Helvetica, sans-serif;
 +
        padding-bottom: 30px;
 +
    }
 
</style>
 
</style>
</head>
+
<body style="width:1263px; margin-left:auto;margin-right:auto;background-color:white" onscroll="scrollEvent()">
<body>
+
    <div id="body">
+
         <!--default for floating navigation-->
    <header>
+
        <div id="sidebar" class="paper-sidenav">
        <div class="site-logo">
+
            <img src="https://static.igem.org/mediawiki/2017/5/57/RDFZ_logo.png">
+
         </div>
+
 
+
        <nav class="site-nav">
+
           
+
 
             <ul>
 
             <ul>
                 <li class="home">
+
                 <li>
                    <a href="https://2018.igem.org/Team:RDFZ-China">HOME</a>
+
                   
+
                </li>
+
               
+
                <li class="project">
+
                    <a href="https://2017.igem.org/Team:RDFZ-China/Description">PROJECT </a>
+
 
                     <ul>
 
                     <ul>
                         <li><a href="https://2018.igem.org/Team:RDFZ-China/Description">BACKGROUND</a></li>
+
                         <li><a href="#section1">What are we facing?</a></li>
                         <li><a href="https://2018.igem.org/Team:RDFZ-China/Description">PROJECT</a></li>
+
                        <li><a href="#section2">Predecessors</a></li>
                         <li><a href="https://2018.igem.org/Team:RDFZ-China/Improve">IMPROVE</a></li>
+
                        <li><a href="#section3">Project Xscape</a></li>
 +
                         <li><a href="#section4">For Fermentation</a></li>
 +
                        <li><a href="#section5">For Therapy</a></li>
 +
                        <li><a href="#section6">Metabolic Stress</a></li>
 +
                         <li><a href="#section7">DIY Bio and Biosafety</a></li>
 +
                        <li><a href="#section8">Community and Future</a></li>
 +
                        <li><a href="#section9">References</a></li>
 
                     </ul>
 
                     </ul>
 
                 </li>
 
                 </li>
               
 
                <li class="experiment">
 
                    <a href="https://2017.igem.org/Team:RDFZ-China/Applied_Design">EXPERIMENT</a>
 
                    <ul>
 
                        <li><a href="https://2018.igem.org/Team:RDFZ-China/Experiments">EXPERIMENT</a></li>
 
                        <li><a href="https://2018.igem.org/Team:RDFZ-China/InterLab">INTERLAB</a></li>
 
                    </ul>
 
                </li>
 
               
 
                <li class="model">
 
                    <a href="https://2018.igem.org/Team:RDFZ-China/Model">MODEL</a>
 
                <ul>
 
                        <li><a href="https://2018.igem.org/Team:RDFZ-China/Model">MODEL</a></li>
 
                        <li><a href="https://2018.igem.org/Team:RDFZ-China/Measurement">MEASUREMENT</a></li>
 
                    </ul>
 
                </li>
 
               
 
                <li class="humanPractice">
 
                    <a href="https://2018.igem.org/Team:RDFZ-China/Human_Practices">HUMAN<br>PRACTICE</a>
 
                    <ul>
 
                        <li><a href="https://2018.igem.org/Team:RDFZ-China/Human_Practices">HUMAN PRACTICE</a></li>
 
                        <li><a href="https://2018.igem.org/Team:RDFZ-China/Public_Engagement">ENGAGEMENT</a></li>
 
                        <li><a href="https://2018.igem.org/Team:RDFZ-China/Public_Engagement">GOLD INTEGRATED</a></li>
 
                    </ul>
 
                </li>
 
               
 
                <li class="demonstrate"><a href=" https://2018.igem.org/Team:RDFZ-China/Demonstrate">DEMONSTRATE</a>
 
                <ul>
 
                <li><a href=" https://2018.igem.org/Team:RDFZ-China/Demonstrate">DEMONSTRATE</a></li>
 
                <li><a href="https://2018.igem.org/Team:RDFZ-China/Applied_Design">APPLIED DESIGN</a></li>
 
                </ul>
 
                </li>
 
               
 
                <li class="safety"><a href="https://2018.igem.org/Team:RDFZ-China/Safety">SAFETY</a>
 
                </li>
 
               
 
                <li class="attribution"><a href="https://2018.igem.org/Team:RDFZ-China/Attributions">Attribution</a>
 
                <ul>
 
                <li><a href="https://2018.igem.org/Team:RDFZ-China/Attributions">ATTRIBUTION</a></li>
 
                <li><a href="https://2018.igem.org/Team:RDFZ-China/Collaborations">COLLABORATION</a></li>
 
                </ul>
 
                </li>
 
               
 
                <li class="team"><a href="https://2017.igem.org/Team:RDFZ-China/Model">TEAM</a>
 
                <ul>
 
                <li><a href="https://2018.igem.org/Team:RDFZ-China/Team">MEMBERS</a></li>
 
                <li><a href="https://2018.igem.org/Team:RDFZ-China/Team">SCHOOLS</a></li>
 
                </ul>
 
                </li>
 
       
 
 
             </ul>
 
             </ul>
         </nav>
+
         </div>
    </header>
+
        <div id="comic">
 +
            <p>
 +
                <img src="https://static.igem.org/mediawiki/2018/thumb/1/18/T--RDFZ-China--PJDhead1263620.jpg/800px-T--RDFZ-China--PJDhead1263620.jpg" alt="pdcomic" />
 +
            </p>
 +
        </div>
 +
        <div class="description">
 +
            <div class="topic-title" id="section1">
 +
                <h3>What are we facing?</h3>
 +
                <p>Biosafety has always been the major concern to the public, to the companies and the researchers. Doubts and worries raised just as genetic technology was invented. With the rapidly growing of synthetic biology and iGEM community, more and more synthetic biology products are built with the widely distributed DNA toolkits or the inexpensive DNA synthesis service(Synthetic and Will); we are facing unprecedented biosafety issue that unwanted leakage of synthetic biology products to the environment may cause an unexpected but definitely disastrous problem. </p>
 +
            </div>
 +
            <div class="topic-title" id="section2">
 +
                <h3>Predecessors</h3>
 +
                <p>For decades, researchers were striving to build biosafety devices through auxotrophy or external inducive kill switches(Lee et al.), holins and restriction enzymes are most commonly used. Most of the failures of the previous devices were caused by mutation and evolution of immune(Moe-Behrens et al.) . </p>
 +
                <p>The two major threats of engineered microbes’ leakage are the possible Horizontal Gene Transfer which will lead to the spread of recombinant DNA to the entire ecosystem, or the engineered bacteria could contaminate or overrun the natural habitat.(Wright et al.)</p>
 +
            </div>
 +
            <div class="topic-title" id="section3">
 +
                <h3>Project Xscape</h3>
 +
                <p>Under this circumstance, this year we decided to be a fundamentalist to synthetic biology, by using genetic circuits and logic gates, to establish biosafety devices which can apply to the real-world situation.</p>
 +
                <p>Since cell death and lysis mean there is a continual presence of free DNA in the environment, holins, which are most widely used are excluded from our choices, and colicin E2 nucleases (Darmstadt iGEM2016) came into our site. We choose site non-specific nucleases since the entire genome and plasmids needed to be entirely digested to prevent the spread, and we use nucleases from a different family to prevent the possible evolution of nuclease inhibitors. Artificial DNA, RNA, and amino acids are a good solution, but due to its high cost so far, it is not applicable to most of the user.</p>
  
        <div id="topicimg">
+
            </div>
<img src = "https://static.igem.org/mediawiki/2018/8/8e/T--RDFZ-China--InterLab2.jpg" alt = "Spread plates" width="100%">
+
            <div class="topic-title" id="section4">
</div>
+
                <h3>For fermentation</h3>
<!--<main>
+
                <p>The first device we build is for the fermentation; we want to execute the escaped engineered bacteria from the fermenter, accidentally or intentionally. We used two environment factors to monitor the bacteria’s situation: temperature and population density, they are both high and tunable in the fermenter. So, the device will initiate when temperature and density are both low. We used thermal sensitive regulator (NUS iGEM2017)(Piraner et al.) and quorum sensing regulator (MIT iGEM2004) (Canton et al.)as our sensor, sRNA(Storz et al.) and tetR family repressor PhlF(Glasgow iGEM2015)(Stanton et al.) as the signal inverter. We add intergrase (Peking iGEM2017) controlled by the thermal sensitive regulator, which will turn the promoter of a lethal gene when temperature rise in the fermenter so that bacteria can survive at the very beginning. Also, we build a model to stimulate the minimum autoinducer required at the beginning of the fermentation, same as the purpose of integrase. This model is for keeping bacteria alive at the very beginning of fermentation. Together they form a NOR gate which will lead to cell death through genome degradation when temperature and density decrease.</p>
 +
            </div>
 +
            <div class="topic-title" id="section5">
 +
                <h3>For Therapy</h3>
 +
                <p>The second device we build is for therapeutic bacteria, the device can carry out noninvasive tracing through ultrasound imaging of the gas vesicle(Shapiro et al.), release the drug (from SHSBNU 2017) controlled by a thermal sensitive regulator at nidus by ultrasound tissue heating, and heat to a higher temperature to release nuclease and kill the bacteria after it finishes its mission. </p>
 +
            </div>
 +
            <div class="topic-title" id="section6">
 +
                <h3>For Metabolic Stress</h3>
 +
                <p>We applied capacity monitor (Ceroni et al.) to quantify the expression burden of all our systems, and to reduce the metabolic stress, we designed another device for fermentation which used a LuxR repressive promoter (Peking iGEM2011) and cold-regulated 5’UTR region (Ionis Paris 2017). This device only involves one transcriptional regulator, which will be less energy consuming. </p>
 +
            </div>
 +
            <div class="topic-title" id="section7">
 +
                <h3>DIY bio and Biosafey</h3>
 +
                <p>Back to the growing and glowing synthetic biology community, despite the ones doing it on campus, more and more people are starting it at home, they call themselves Genehacker or DIY biologists. The lack of sufficient training and efficient surveillance will be a time bomb which we do know there will be a monstrous harmful bioproduct will be made someday in the future, and indeed, it will be a significant threat to the current biosafety basis. Recall our memory to iGEM2009, Peking surveyed DIY bio, almost ten years later, we conducted a similar DIY bio-survey again. We tried to order materials for molecular experiments, using the delivery address to our home, the result was quite shocking that we can buy almost everything for the molecular experiment, from the internet. Then, we went through relevant laws and regulations throughout the world, which we found out that there are no laws related to the credit certification and the address certification about the people who book the biology reagent. Most of the laws are about the quality certification and how they would serve the user after they bought this. We interviewed the Director of the center for disease control and prevention. He said that within his experiment with the disease caused by the Bacteria leak, environmental pollution, the vast impact had been caused. Our country has been making all effort which is the highest effort that we have made in the history. He said it is not easy to solve the problem with hard work, it needs the cooperation between all the countries. He made an example of 731 army during the second world war two, the outbreak of pathogens can cause significant social harm. We are still on our way to win the battle, but the effort still needs to be put in.</p>
 +
            </div>
 +
            <div class="topic-title" id="section8">
 +
                <h3>Community and Future</h3>
 +
                <p>Also, we hosted two major meeting in Beijing, a Biosafety Forum in October, we invited team leader who runs his high school lab, lab teacher from a university lab, and a former team member from Peking iGEM2009, who participated in that DIY bio investigation ten years ago.</p>
 +
                <p>We concluded that the development of DIY bio should be taken seriously, and the permanent way to solve it is through implanting Biosafety awareness into our academic culture. Also, as iGEMer, we should strive to be the considerable and responsible leaders in our community, to ensure the biosafety issue has been taken properly. Another meeting was with biology Olympians all around China, we discussed the future of biology community during the meeting, especially with more and more high school iGEM teams coming up in China, but lack of relevant instruction and education to the students. We came up with the idea of setting up a collaboration between school to share and overcome difficulties hand in hand. This kind of meeting will be continued after iGEM2018, since the community usually grows fast after every iGEM season. </p>
 +
                <p>Hopefully, years later, biosafety awareness and considerations can be seriously taken in communities, laboratory studies, and real-world applications.</p>
 +
            </div>
 +
            <br>
 +
            <br>
 +
         
 +
        </div>
 +
        <div class="reference">
 +
            <div class="topic-title" id="section9">
 +
                <h3>References</h3>
 +
                <p>Canton, Barry, et al. “Refinement and Standardization of Synthetic Biological Parts and Devices.” Nature Biotechnology, vol. 26, no. 7, 2008, pp. 787–93, doi:10.1038/nbt1413.</p>
 +
                <p>Ceroni, Francesca, et al. “Quantifying Cellular Capacity Identifies Gene Expression Designs with Reduced Burden.” Nature Methods, vol. 12, no. 5, 2015, pp. 415–18, doi:10.1038/nmeth.3339.</p>
 +
                <p>Lee, Jeong Wook, et al. “Next-Generation Biocontainment Systems for Engineered Organisms.” Nature Chemical Biology, Springer US, 2018, p. 1, doi:10.1038/s41589-018-0056-x.</p>
 +
                <p>Moe-Behrens, Gerd H. G., et al. “Preparing Synthetic Biology for the World.” Frontiers in Microbiology, vol. 4, no. JAN, 2013, pp. 1–10, doi:10.3389/fmicb.2013.00005.</p>
 +
                <p>Piraner, Dan I., et al. “Tunable Thermal Bioswitches for in Vivo Control of Microbial Therapeutics.” Food, Pharmaceutical and Bioengineering Division 2017 - Core Programming Area at the 2017 AIChE Annual Meeting, vol. 2, no. November, Nature Publishing Group, 2017, pp. 695–702, doi:10.1038/nchembio.2233.</p>
 +
                <p>Shapiro, Mikhail G., et al. “Biogenic Gas Nanostructures as Ultrasonic Molecular Reporters.” Nature Nanotechnology, vol. 9, no. 4, Nature Publishing Group, 2014, pp. 311–16, doi:10.1038/nnano.2014.32.</p>
 +
                <p>Stanton, Brynne C., et al. “Genomic Mining of Prokaryotic Repressors for Orthogonal Logic Gates.” Nature Chemical Biology, vol. 10, no. 2, 2014, pp. 99–105, doi:10.1038/nchembio.1411.</p>
 +
                <p>Storz, Gisela, et al. “Regulation by Small RNAs in Bacteria: Expanding Frontiers.” Molecular Cell, vol. 43, no. 6, 2011, pp. 880–91, doi:10.1016/j.molcel.2011.08.022.</p>
 +
                <p>Synthetic, How, and Biology Will. “Regenesis: How Synthetic Biology Will Reinvent Nature and Ourselves.” Choice Reviews Online, 2013, doi:10.5860/CHOICE.50-3835.</p>
 +
                <p>Wright, Oliver, et al. “Building-in Biosafety for Synthetic Biology.” Microbiology (United Kingdom), vol. 159, no. PART7, 2013, pp. 1021–35, doi:10.1099/mic.0.066308-0.</p>
 +
            </div>
  
<section class = "interlab">
+
        </div>
      <h1 style = "text-align: center">InterLab</h1>
+
 
+
      <hr class="line">
+
 
+
<div>
+
<h1>Introduction: What is InterLab</h1>
+
<p>Reliable and repeatable measurement is key to synthetic biology. It is essential for a standard protocol to be established so that the same measurements can be repeated in different labs. This year's interlab study is aimed to reduce the variability of cell count measurements by replacing OD600 measurement which varies between labs with directly counting of colony forming units (CFU) to determine the number of cells in each sample. Then the mean GFP expression level by each cell can be determined by dividing the already standardized GFP expression level of the sample by the number of cells in that sample.
+
<br>
+
<br>
+
This is the 5th year of InterLab and we have the following question:
+
<br>
+
<b>
+
<font color = "orange" size = "5" face = "serif">
+
Can we reduce lab-to-lab variability in fluorescence measurements by normalizing to absolute cell count or colony-forming units (CFUs) instead of OD?
+
</font>
+
</b>
+
</p>
+
+
</div>
+
+
<div>
+
<h1>Materials</h1>
+
<p>DNA/Plasmids</p>
+
<ol>
+
<li>Negative Control: BBa_R0040</li>
+
<li>Positive Control: BBa_I20270</li>
+
<li>Test Device 1: BBa_J364000</li>
+
<li>Test Device 2: BBa_J364001</li>
+
<li>Test Device 3: BBa_J364002</li>
+
<li>Test Device 4: BBa_J364007</li>
+
<li>Test Device 5: BBa_J364008</li>
+
<li>Test Device 6: BBa_J364009</li>
+
</ol>
+
<p>Apparatus</p >
+
<ul>
+
<li>96 well plates (provided by Peking University)</li>
+
<li>Plate reader</li>
+
<li>Foil covered 50 ml tube</li>
+
<li>Eppendorf tubes</li>
+
<li>Pipettes</li>
+
</ul>
+
<p>Materials</p>
+
<ul>
+
<li>LUDOX CL-X</li>
+
<li>Silica beads</li>
+
<li>Fluorescein</li>
+
<li>Phosphate buffered saline</li>
+
<li>LB media</li>
+
<li>Chloramphenicol</li>
+
<li>LB plates</li>
+
<li>distilled water</li>
+
</ul>
+
</div>
+
+
<div>
+
<h1>Protocols</h1>
+
<div>
+
<p> We followed the protocol provided by iGEM HQ so that inter-laboratory errors can be reduced. Protocols we used can be found here:</p>
+
<a href = "https://static.igem.org/mediawiki/2018/0/09/2018_InterLab_Plate_Reader_Protocol.pdf"> 2018 InterLab Plate Reader Protocol</a><br>
+
<a href = "http://parts.igem.org/Help:Protocols/Transformation">Help: Protocols/Transformation</a>
+
</div>
+
<div>
+
<p>During the first day, we resuspended DNA from distribution kit <em>(Kit Open Day!)</em> and transformed the plasmids into <i>Escherichia coli</i> DH5<i>α</i> competent cells.</p>
+
<img src = "https://static.igem.org/mediawiki/2018/6/6b/T--RDFZ-China--InterLab1.jpeg" alt = "Open Distribution Kit" style = "width: 30%">
+
</div>
+
<div>
+
<p>For the second day, firstly we picked single colonies from transformation plates and prepared overnight cultures; we also finished particle and fluorescence calibration.</p>
+
<img src = "https://static.igem.org/mediawiki/2018/6/6f/T--RDFZ-China--InterLab5.jpeg" alt = "Add silica beads to 96 well plate" style = "width: 30%">
+
</div>
+
<div>
+
<p>The third day was fairly occupied.</p>
+
<ol>
+
<li>Overnight cultures were collected for assays. Essentially, each culture was diluted into same starting Abs readings and incubated for 6 hours. Samples were taken at the starting time and after 6 hours. Abs and fluorescence readings were measured for each sample and then imported into excel file.</li>
+
<li>While we were waiting for incubation, we diluted the starting sample culture for Colony Forming Units protocols and spread 36 LB plates.</li>
+
<li>We nearly forgot to calibrate OD reference points at the end of the day!</li>
+
</ol>
+
<img src = "https://static.igem.org/mediawiki/2018/8/8e/T--RDFZ-China--InterLab2.jpg" alt = "Spread plates" width = "30%">
+
<img src = "https://static.igem.org/mediawiki/2018/d/d0/T--RDFZ-China--InterLab3.jpeg" alt = "Add cultures to 96 well plate" width = "30%">
+
<img src = "https://static.igem.org/mediawiki/2018/8/83/T--RDFZ-China--InterLab4.jpeg" alt = "With the PLATE READER!" width = "30%">
+
</div>
+
<div>
+
<p>At last, we counted the colonies <em>(colony forming units)</em> in those 36 plates. It was just an exhausting process!</p>
+
</div>
+
</div>
+
+
<div>
+
<h1>Results</h1>
+
<p><i>The results are shown in the tables and figures.</i></p>
+
<h2>Calibrations</h2>
+
<div class="inlabdiv">
+
<p>OD<sub>600</sub> reference point:</p>
+
<img src = "https://static.igem.org/mediawiki/2018/0/0a/T--RDFZ-China--OD600_Reference_Point.png" alt = "OD600 Reference Point" style = "width: 30%"><br>
+
<font size = "1">Table 1. OD600 Reference Point.</font>
+
</div>
+
 
+
<div class="inlabdiv">
+
                                <p>Particle Standard Curve</p>
+
<img src = "https://static.igem.org/mediawiki/2018/7/76/T--RDFZ-China--Fluorescein_Standard_Curve.png" alt = "Fluorescein Standard Curve" style = "width: 50%"><br>
+
<font size = "1">Figure 1. Particle Standard Curve.</font>
+
</div>
+
<div class="inlabdiv">
+
                                <p>Fluorescein Standard Curve</p>
+
<img src = "https://static.igem.org/mediawiki/2018/b/b9/T--RDFZ-China--Particle_Standard_Curve.png" alt = "Particle Standard Curve" style = "width: 50%"><br>
+
<font size = "1">Figure 2. Fluorescein Standard Curve.</font>
+
</div>
+
<h2>Raw Plate Reader Measurements</h2>
+
<div class="inlabdiv">
+
<p><b>Fluorescence Raw</b></p>
+
<img src = "https://static.igem.org/mediawiki/2018/7/74/T--RDFZ-China--Fluorescence_Raw_0_hour.png" alt = "Fluorescence at 0h" style = "width: 50%"><br>
+
<font size = "1">Table 2. Raw Plate Reader Measurements of Fluorescence Raw at 0 hour.</font>
+
</div>
+
<div class = "inlabdiv">
+
<img src = "https://static.igem.org/mediawiki/2018/0/0c/T--RDFZ-China--Fluorescence_Raw_6_hours.png" alt = "Fluorescence at 6h" style = "width: 50%"><br>
+
<font size = "1">Table 3. Raw Plate Reader Measurements of Fluorescence Raw at 6 hours.</font>
+
</div>
+
<div class = "inlabdiv">
+
<p><b>Abs<sub>600</sub> Raw</b></p>
+
<img src = "https://static.igem.org/mediawiki/2018/c/ce/T--RDFZ-China--Abs600_Raw_0_hour.png" alt = "Abs600 at 0h" style = "width: 50%"><br>
+
<font size = "1">Table 4. Raw Plate Reader Measurements of Abs600 Raw at 0 hour.</font>
+
</div>
+
<div class = "inlabdiv">
+
<img src = "https://static.igem.org/mediawiki/2018/8/89/T--RDFZ-China--Abs600_Raw_6_hours.png" alt = "Abs600 at 6h" style = "width: 50%"><br>
+
<font size = "1">Table 5. Raw Plate Reader Measurements of Abs600 Raw at 6 hours.</font>
+
</div>
+
<div class = "inlabdiv">
+
                                <p><b>CFU counts</b></p>
+
<table style = "width: 70%; height: 200px;">
+
<tr>
+
<th>Device</th>
+
<th>Dilution Factor</th>
+
<th>CFU Replicate 1</th>
+
<th>CFU Replicate 2</th>
+
<th>CFU Replicate 3</th>
+
</tr>
+
<tr>
+
<td rowspan="3">Positive Control 1</td>
+
<td>8*10<sup>4</sup></td>
+
<td>69</td>
+
<td>22</td>
+
<td>191</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>5</sup></td>
+
<td>5</td>
+
<td>2</td>
+
<td>5</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>6</sup></td>
+
<td>1</td>
+
<td>0</td>
+
<td>0</td>
+
</tr>
+
<tr>
+
<td rowspan="3">Positive Control 2</td>
+
<td>8*10<sup>4</sup></td>
+
<td>1</td>
+
<td>15</td>
+
<td>65</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>5</sup></td>
+
<td>1</td>
+
<td>1</td>
+
<td>5</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>6</sup></td>
+
<td>0</td>
+
<td>0</td>
+
<td>1</td>
+
</tr>
+
<tr>
+
<td rowspan="3">Negative Control 1</td>
+
<td>8*10<sup>4</sup></td>
+
<td>98</td>
+
<td>164</td>
+
<td>85</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>5</sup></td>
+
<td>85</td>
+
<td>29</td>
+
<td>48</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>6</sup></td>
+
<td>19</td>
+
<td>63</td>
+
<td>23</td>
+
</tr>
+
<tr>
+
<td rowspan="3">Negative Control 2</td>
+
<td>8*10<sup>4</sup></td>
+
<td>190</td>
+
<td>226</td>
+
<td>274</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>5</sup></td>
+
<td>52</td>
+
<td>54</td>
+
<td>49</td>
+
</tr>
+
<tr>
+
<td>8*10<sup>6</sup></td>
+
<td>78</td>
+
<td>20</td>
+
<td>24</td>
+
</tr>
+
</table>
+
<font size = "2">Table 6. Colony Forming Unit Counts.</font>
+
      </div>
+
</div>
+
 
+
<div>
+
<h1>Evaluation</h1>
+
<p>The control LB measures in Table 4 and Table 5 are a little different, since we changed the LB control after dilution: two different bottle of LB with Chl were measured. The CFU counts in same dilution factor show great variation <b>(Table 6)</b>. High variation may result from the difference of experimenters' spreading methods or fluctuations in the starting sample <em>(starting samples were diluted to OD<sub>600</sub>=0.1 approxiamately)</em>.</p>
+
</div>
+
+
<div>
+
<h1>Our Thoughts</h1>
+
<p><em>Yishen Shen:</em><br>Although it's not my first time to participate in an experiment, I still learned a lot from the InterLab.  With so many steps in protocols out there, it can be overwhelming to get started right away. I learned that I should copy down all protocols down on notebook beforehand; it's much easier to follow a protocol that I have written and analyzed by myself.  Also, it's handy to obtain all the necessary reagents in advance and make sure they are all in good conditions. I used to run out for reagent in the middle of an experiment and that makes it hectic and messy. Furthermore, I get to know that preparing a timeline is the key. Dividing a day into various blocks keeps me busy and efficient. The three-day experience in InterLab teaches me a lot, though it's mostly repetitive, I got to acquire new knowledge every day and that makes it memorable.</p>
+
<p><em>Jianxiang Zhang:</em><br>We feel like that the protocol can sometimes be ambiguous. For instance, the protocol says to "check the OD<sub>600</sub> and make sure it is 0.1 (minus the blank measurement)", it is kind of confusing about how to interpret the content inside the parentheses. Overall, the InterLab study is helpful for providing new measuring methods to our later part characterization study.</p>
+
</div>
+
+
<div>
+
<h1>Acknowledgements</h1>
+
<p><em>Thanks to Molecular Biology Laboratory in Tsinghua University, we could follow the protocols without issues regarding apparatus and reagents. Also, we'd like to appreciate our advisor and anyone who helped us in Tsinghua and Peking University for providing suggestions and guidance during InterLab studies.</em></p>
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Revision as of 10:01, 17 October 2018

pdcomic

What are we facing?

Biosafety has always been the major concern to the public, to the companies and the researchers. Doubts and worries raised just as genetic technology was invented. With the rapidly growing of synthetic biology and iGEM community, more and more synthetic biology products are built with the widely distributed DNA toolkits or the inexpensive DNA synthesis service(Synthetic and Will); we are facing unprecedented biosafety issue that unwanted leakage of synthetic biology products to the environment may cause an unexpected but definitely disastrous problem.

Predecessors

For decades, researchers were striving to build biosafety devices through auxotrophy or external inducive kill switches(Lee et al.), holins and restriction enzymes are most commonly used. Most of the failures of the previous devices were caused by mutation and evolution of immune(Moe-Behrens et al.) .

The two major threats of engineered microbes’ leakage are the possible Horizontal Gene Transfer which will lead to the spread of recombinant DNA to the entire ecosystem, or the engineered bacteria could contaminate or overrun the natural habitat.(Wright et al.)

Project Xscape

Under this circumstance, this year we decided to be a fundamentalist to synthetic biology, by using genetic circuits and logic gates, to establish biosafety devices which can apply to the real-world situation.

Since cell death and lysis mean there is a continual presence of free DNA in the environment, holins, which are most widely used are excluded from our choices, and colicin E2 nucleases (Darmstadt iGEM2016) came into our site. We choose site non-specific nucleases since the entire genome and plasmids needed to be entirely digested to prevent the spread, and we use nucleases from a different family to prevent the possible evolution of nuclease inhibitors. Artificial DNA, RNA, and amino acids are a good solution, but due to its high cost so far, it is not applicable to most of the user.

For fermentation

The first device we build is for the fermentation; we want to execute the escaped engineered bacteria from the fermenter, accidentally or intentionally. We used two environment factors to monitor the bacteria’s situation: temperature and population density, they are both high and tunable in the fermenter. So, the device will initiate when temperature and density are both low. We used thermal sensitive regulator (NUS iGEM2017)(Piraner et al.) and quorum sensing regulator (MIT iGEM2004) (Canton et al.)as our sensor, sRNA(Storz et al.) and tetR family repressor PhlF(Glasgow iGEM2015)(Stanton et al.) as the signal inverter. We add intergrase (Peking iGEM2017) controlled by the thermal sensitive regulator, which will turn the promoter of a lethal gene when temperature rise in the fermenter so that bacteria can survive at the very beginning. Also, we build a model to stimulate the minimum autoinducer required at the beginning of the fermentation, same as the purpose of integrase. This model is for keeping bacteria alive at the very beginning of fermentation. Together they form a NOR gate which will lead to cell death through genome degradation when temperature and density decrease.

For Therapy

The second device we build is for therapeutic bacteria, the device can carry out noninvasive tracing through ultrasound imaging of the gas vesicle(Shapiro et al.), release the drug (from SHSBNU 2017) controlled by a thermal sensitive regulator at nidus by ultrasound tissue heating, and heat to a higher temperature to release nuclease and kill the bacteria after it finishes its mission.

For Metabolic Stress

We applied capacity monitor (Ceroni et al.) to quantify the expression burden of all our systems, and to reduce the metabolic stress, we designed another device for fermentation which used a LuxR repressive promoter (Peking iGEM2011) and cold-regulated 5’UTR region (Ionis Paris 2017). This device only involves one transcriptional regulator, which will be less energy consuming.

DIY bio and Biosafey

Back to the growing and glowing synthetic biology community, despite the ones doing it on campus, more and more people are starting it at home, they call themselves Genehacker or DIY biologists. The lack of sufficient training and efficient surveillance will be a time bomb which we do know there will be a monstrous harmful bioproduct will be made someday in the future, and indeed, it will be a significant threat to the current biosafety basis. Recall our memory to iGEM2009, Peking surveyed DIY bio, almost ten years later, we conducted a similar DIY bio-survey again. We tried to order materials for molecular experiments, using the delivery address to our home, the result was quite shocking that we can buy almost everything for the molecular experiment, from the internet. Then, we went through relevant laws and regulations throughout the world, which we found out that there are no laws related to the credit certification and the address certification about the people who book the biology reagent. Most of the laws are about the quality certification and how they would serve the user after they bought this. We interviewed the Director of the center for disease control and prevention. He said that within his experiment with the disease caused by the Bacteria leak, environmental pollution, the vast impact had been caused. Our country has been making all effort which is the highest effort that we have made in the history. He said it is not easy to solve the problem with hard work, it needs the cooperation between all the countries. He made an example of 731 army during the second world war two, the outbreak of pathogens can cause significant social harm. We are still on our way to win the battle, but the effort still needs to be put in.

Community and Future

Also, we hosted two major meeting in Beijing, a Biosafety Forum in October, we invited team leader who runs his high school lab, lab teacher from a university lab, and a former team member from Peking iGEM2009, who participated in that DIY bio investigation ten years ago.

We concluded that the development of DIY bio should be taken seriously, and the permanent way to solve it is through implanting Biosafety awareness into our academic culture. Also, as iGEMer, we should strive to be the considerable and responsible leaders in our community, to ensure the biosafety issue has been taken properly. Another meeting was with biology Olympians all around China, we discussed the future of biology community during the meeting, especially with more and more high school iGEM teams coming up in China, but lack of relevant instruction and education to the students. We came up with the idea of setting up a collaboration between school to share and overcome difficulties hand in hand. This kind of meeting will be continued after iGEM2018, since the community usually grows fast after every iGEM season.

Hopefully, years later, biosafety awareness and considerations can be seriously taken in communities, laboratory studies, and real-world applications.



References

Canton, Barry, et al. “Refinement and Standardization of Synthetic Biological Parts and Devices.” Nature Biotechnology, vol. 26, no. 7, 2008, pp. 787–93, doi:10.1038/nbt1413.

Ceroni, Francesca, et al. “Quantifying Cellular Capacity Identifies Gene Expression Designs with Reduced Burden.” Nature Methods, vol. 12, no. 5, 2015, pp. 415–18, doi:10.1038/nmeth.3339.

Lee, Jeong Wook, et al. “Next-Generation Biocontainment Systems for Engineered Organisms.” Nature Chemical Biology, Springer US, 2018, p. 1, doi:10.1038/s41589-018-0056-x.

Moe-Behrens, Gerd H. G., et al. “Preparing Synthetic Biology for the World.” Frontiers in Microbiology, vol. 4, no. JAN, 2013, pp. 1–10, doi:10.3389/fmicb.2013.00005.

Piraner, Dan I., et al. “Tunable Thermal Bioswitches for in Vivo Control of Microbial Therapeutics.” Food, Pharmaceutical and Bioengineering Division 2017 - Core Programming Area at the 2017 AIChE Annual Meeting, vol. 2, no. November, Nature Publishing Group, 2017, pp. 695–702, doi:10.1038/nchembio.2233.

Shapiro, Mikhail G., et al. “Biogenic Gas Nanostructures as Ultrasonic Molecular Reporters.” Nature Nanotechnology, vol. 9, no. 4, Nature Publishing Group, 2014, pp. 311–16, doi:10.1038/nnano.2014.32.

Stanton, Brynne C., et al. “Genomic Mining of Prokaryotic Repressors for Orthogonal Logic Gates.” Nature Chemical Biology, vol. 10, no. 2, 2014, pp. 99–105, doi:10.1038/nchembio.1411.

Storz, Gisela, et al. “Regulation by Small RNAs in Bacteria: Expanding Frontiers.” Molecular Cell, vol. 43, no. 6, 2011, pp. 880–91, doi:10.1016/j.molcel.2011.08.022.

Synthetic, How, and Biology Will. “Regenesis: How Synthetic Biology Will Reinvent Nature and Ourselves.” Choice Reviews Online, 2013, doi:10.5860/CHOICE.50-3835.

Wright, Oliver, et al. “Building-in Biosafety for Synthetic Biology.” Microbiology (United Kingdom), vol. 159, no. PART7, 2013, pp. 1021–35, doi:10.1099/mic.0.066308-0.

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