Difference between revisions of "Team:SPSingapore/Safety"

 
(16 intermediate revisions by the same user not shown)
Line 53: Line 53:
 
}
 
}
  
a,a:hover{text-decoration:none;color: #ff7f00;}
+
a,a:hover,a:visited{text-decoration:none;color: #ff7f00;}
 
</style>
 
</style>
 
</head>
 
</head>
Line 63: Line 63:
 
<div class = "logo">
 
<div class = "logo">
 
</div>
 
</div>
 +
  
 
<div id='cssmenu'>
 
<div id='cssmenu'>
 
<ul>
 
<ul>
  <li><a href='https://2015.igem.org/Team:SPSingapore/'><span>Home</span></a></li>
+
<li class = 'active'><a href='https://2015.igem.org/Team:SPSingapore/'><span>Home</span></a></li>
  <li><a href='https://2015.igem.org/Team:SPSingapore/Team'><span>Team</span></a></li>
+
<li><a href='https://2015.igem.org/Team:SPSingapore/Team'><span>Team</span></a>
  <li><a href='https://2015.igem.org/Team:SPSingapore/Project'><span>Project</span></a></li>
+
<ul>
  <li><a href='https://2015.igem.org/Team:SPSingapore/Protocol'><span>Protocol</span></a></li>
+
<li><a href="https://2015.igem.org/Team:SPSingapore/Team">Overview</a></li>
  <li><a href='https://2015.igem.org/Team:SPSingapore/Parts'><span>Parts</span></a></li>
+
<li><a href="https://igem.org/Team.cgi?id=1804">Official Profile</a></li>
  <li><a href='https://2015.igem.org/Team:SPSingapore/Notebook'><span>Notebook</span></a></li>
+
        <li><a href="https://2015.igem.org/Team:SPSingapore/Team Bios">Team Bios</a></li>
  <li><a href='https://2015.igem.org/Team:SPSingapore/Practices'><span>Human Practices</span></a></li>
+
        <li><a href="https://2015.igem.org/Team:SPSingapore/Mentors">Mentors</a></li>
  <li class = 'active'><a href='https://2015.igem.org/Team:SPSingapore/Safety'><span>Safety</span></a></li>
+
        <li><a href="https://2015.igem.org/Team:SPSingapore/Attributions">Attributions</a></li>
 +
</ul>
 +
</li>
 +
<li><a href='https://2015.igem.org/Team:SPSingapore/Project'><span>Project</span></a>
 +
<ul>
 +
<li><a href='https://2015.igem.org/Team:SPSingapore/Project'>Overview</a></li>
 +
        <li><a href="https://2015.igem.org/Team:SPSingapore/Invasin">Invasin + Listerolysin</a></li>
 +
        <li><a href="https://2015.igem.org/Team:SPSingapore/ESAQS">esa Quorum Sensing</a></li>
 +
        <li><a href="https://2015.igem.org/Team:SPSingapore/Anaerobic Promoter">Anaerobic Promoter</a></li>
 +
        <li><a href="https://2015.igem.org/Team:SPSingapore/Parts">Parts</a></li>
 +
</ul>
 +
</li>
 +
<li><a href='https://2015.igem.org/Team:SPSingapore/Notebook'><span>Notebook</span></a>
 +
<ul>
 +
<li><a href="https://2015.igem.org/Team:SPSingapore/Protocol">Protocols</a></li>
 +
        <li><a href="https://2015.igem.org/Team:SPSingapore/Notebook">Entries</a></li>
 +
</ul>
 +
</li>
 +
<li><a href='https://2015.igem.org/Team:SPSingapore/Practices'><span>Human Practices</span></a>
 +
<ul>
 +
<li><a href="https://2015.igem.org/Team:SPSingapore/Practices">Overview</a></li>
 +
<li><a href="https://2015.igem.org/Team:SPSingapore/Workshop">Workshop</a></li>
 +
<li><a href="https://2015.igem.org/Team:SPSingapore/Workshop Materials">Workshop Materials</a></li>
 +
        <li><a href="https://2015.igem.org/Team:SPSingapore/Interview">Consultations</a></li>
 +
</ul>
 +
</li>
 +
<li><a href='https://2015.igem.org/Team:SPSingapore/Safety'><span>Safety</span></a></li>
 +
<li class='last'><a href='https://2015.igem.org/Team:SPSingapore/Medals'><span>Medals</span></a></li>
 
</ul>
 
</ul>
 
</div>
 
</div>
Line 79: Line 107:
 
<div id='sidemenu' style = "float:left">
 
<div id='sidemenu' style = "float:left">
 
<ul>
 
<ul>
   <li class='last'><a href = "https://2015.igem.org/Team:SPSingapore/Safety"><span>SAFETY</span></a>
+
   <li><a href = "https://2015.igem.org/Team:SPSingapore/Safety"><span>SAFETY</span></a>
 
<ul>
 
<ul>
        <img src = "https://static.igem.org/mediawiki/2015/5/54/SPSingapore_Safety-Logo.png" width = 200px>
+
      <li><a href = "#p1"><span>Biological Safety</span></a></li>
 +
      <li><a href = "#p2"><span>Safety in Project Design</span></a></li>
 +
      <li><a href = "#p3"><span>Lab Safety</span></a></li>
 +
      <li class = 'last'><a href = "#p4"><span>Safety Requirements</span></a></li>
 
       </ul>
 
       </ul>
 
   </li>
 
   </li>
 +
<li class = 'last'>
 +
<a><span style = "background-color:midnightblue"><br>
 +
"Just learning good science is not a justification for putting life and health at risk."<br><br> - Marc Lipsitch
 +
</span></a>
 +
</li>
 
</ul>
 
</ul>
 
</div>
 
</div>
Line 107: Line 143:
  
 
<br>
 
<br>
<!----------------------- Entry Start ------------------------>
 
<center>
 
<table style = "width:600px; border-collapse: collapse;text-align:justify;">
 
<tr>
 
<td>
 
<i>Biosafety in our project involves minimising the risks to the researchers working in the laboratory, as well as the general public in future medical applications based off our research.</i>
 
  
<br><br>
+
<a>
<h3>Safety when handling biological organisms</h3>
+
<div style = "float:right; width:350px;margin-right:20px;">
Non-pathogenic strains of E. coli K-12 strains BL21 and dH5α from Life Technologies were used for bacterial cloning of plasmids and expression of proteins of interest. These strains are Risk group 1 and were handled in a BSL2 Biosafety cabinet. The E. coli strain carrying the Biobrick BBaK299812 (containing parts derived from Risk group 2 organisms) was handled as a Risk Group 2 agent. Mammalian cell line HEK293T is classified under Risk group 2, and was also cultured in a BSL2 Biosafety cabinet.
+
<img src = "https://static.igem.org/mediawiki/2015/c/c9/SPSingapore_Safety_Main.png" width = "350px">
 +
<br>
 +
</div>
 +
</a>
  
 +
<div style = "float:left;width:340px;font-size:14px;text-align:justify;margin-top:20px;margin-left:20px;">
 +
Safety is always of paramount importance in the laboratory, even more so when biological agents are involved. Our team takes safety very seriously and have worked hard to ensure that our procedures are up to scratch.
 
<br><br>
 
<br><br>
 +
Biosafety in our project involves minimising the risks to the researchers working in the laboratory, as well as the general public in future medical applications based off our research.
 +
<br><br>
 +
We are proud that SPS Wet Lab has obtained <font color = "darkviolet"><b> an 'A' grade </b></font> for the FOS Housekeeping Inspection 2015 for lab safety over the summer of 2015 and strive to maintain a safe working environment for all researchers in the lab.
 +
</div>
  
<h3>Safety in Project Design</h3>
+
 
 +
 
 +
<! ----------------------Start of Safety Text --------------------------------->
 +
 
 +
<center>
 +
<table style = "width:700px; border-collapse: collapse; " id = "safety">
 +
 
 +
<!--Protocol 1 -->
 +
 
 +
<tr id = "p1"><td><br><br></td></tr>
 +
 
 +
<tr><td style = "font-size:20px;padding-bottom:10px;"><a><b>
 +
Safety in Handling Biological Organisms
 +
</b></a></td></tr>
 +
 
 +
<tr style = "border-top:2px solid grey;">
 +
<td style="padding-bottom:30px;padding-top:30px;padding-left:60px;padding-right:60px">
 +
 
 +
<div style = "text-align:justify;font-size:14px">
 +
Non-pathogenic strains of E. coli K-12 strains BL21 and dH5α from Life Technologies were used for bacterial cloning of plasmids and expression of proteins of interest. These strains are Risk group 1 and were handled in a BSL2 Biosafety cabinet. The E. coli strain carrying the Biobrick BBaK299812 (containing parts derived from Risk group 2 organisms) was handled as a Risk Group 2 agent. Mammalian cell line HepG2 is classified under Risk group 2, and was also cultured in a BSL2 Biosafety cabinet.
 +
</div>
 +
 
 +
 
 +
</td>
 +
</tr>
 +
 
 +
<! ------P2----->
 +
<tr id = "p2"><td><br></td></tr>
 +
 
 +
<tr><td style = "font-size:20px;padding-bottom:10px;"><a><b>
 +
Safety in Project Design
 +
</b></a></td></tr>
 +
 
 +
<tr style = "border-top:2px solid grey;">
 +
<td style="padding-bottom:30px;padding-top:30px;padding-left:60px;padding-right:60px">
 +
 
 +
<div style = "text-align:justify;font-size:14px">
 
In our project, we aim to engineer non-pathogenic E. coli as a vector to deliver a potential drug into the tumour core. We use the <a href = "http://parts.igem.org/wiki/index.php?title=Part:BBa_K299812">Biobricks Part BBa_K299812</a>, which contains the invasin gene from Yersinia pseudotuberculosis and the listerolysin O gene from Listeria monocytogenes. The Invasin protein allows for bacteria to enter mammalian cells, while Listerolysin O is a pore-forming protein that enable bacteria to escape the endosome. These two proteins are involved in pathogenesis of their respective bacterial species.
 
In our project, we aim to engineer non-pathogenic E. coli as a vector to deliver a potential drug into the tumour core. We use the <a href = "http://parts.igem.org/wiki/index.php?title=Part:BBa_K299812">Biobricks Part BBa_K299812</a>, which contains the invasin gene from Yersinia pseudotuberculosis and the listerolysin O gene from Listeria monocytogenes. The Invasin protein allows for bacteria to enter mammalian cells, while Listerolysin O is a pore-forming protein that enable bacteria to escape the endosome. These two proteins are involved in pathogenesis of their respective bacterial species.
 
<br><br>
 
<br><br>
 
The Invasin and Listerolysin proteins enable our E. coli to enter mammalian cells, and escape the endosome, where they can subsequently deliver an encoded therapeutic to kill the tumour cell. To ensure that these proteins are only expressed under the conditions of the tumour microenvironment, the invasin and listerolysin proteins will be placed under the control of an anaerobic promoter, and a quorum sensing system.
 
The Invasin and Listerolysin proteins enable our E. coli to enter mammalian cells, and escape the endosome, where they can subsequently deliver an encoded therapeutic to kill the tumour cell. To ensure that these proteins are only expressed under the conditions of the tumour microenvironment, the invasin and listerolysin proteins will be placed under the control of an anaerobic promoter, and a quorum sensing system.
 +
</div>
  
<br><br>
+
</td>
 +
</tr>
  
<h3>Safety in Our Lab</h3>
+
<!--Protocol 3 -->
 +
 
 +
<tr id = "p3"><td><br></td></tr>
 +
 
 +
<tr><td style = "font-size:20px;padding-bottom:10px;"><a><b>
 +
Safety in Our Lab
 +
</b></a></td></tr>
 +
 
 +
<tr style = "border-top:2px solid grey;">
 +
<td style="padding-bottom:30px;padding-top:30px;padding-left:60px;padding-right:60px">
 +
 
 +
<div style = "text-align:justify;font-size:14px">
 
All our team members have undergone Chemical, Biological and Fire Safety Training from the <a href = "http://www.nus.edu.sg/osh"> Office of Safety, Health and Environment (OSHE)</a> , the department in charge of Laboratory and Work Safety at the National University of Singapore.
 
All our team members have undergone Chemical, Biological and Fire Safety Training from the <a href = "http://www.nus.edu.sg/osh"> Office of Safety, Health and Environment (OSHE)</a> , the department in charge of Laboratory and Work Safety at the National University of Singapore.
 
<br><br>
 
<br><br>
Line 135: Line 223:
 
<br><br>
 
<br><br>
 
Bacterial work and Mammalian cell culture are performed in separate BSL2 Biosafety Cabinets, while DNA work is done on the bench. No cytotoxic reagents are used in our laboratory; Sybr Safe DNA stain is used rather than Ethidium Bromide. Liquid biological waste is decontaminated using 10% Bleach, while Solid biological waste is sent for incineration in a local incineration plant devoted to medical waste (<a href = "http://www.sembcorp.com/en/business-on-site-services-solid_waste_management.aspx">Sembcorp</a>).
 
Bacterial work and Mammalian cell culture are performed in separate BSL2 Biosafety Cabinets, while DNA work is done on the bench. No cytotoxic reagents are used in our laboratory; Sybr Safe DNA stain is used rather than Ethidium Bromide. Liquid biological waste is decontaminated using 10% Bleach, while Solid biological waste is sent for incineration in a local incineration plant devoted to medical waste (<a href = "http://www.sembcorp.com/en/business-on-site-services-solid_waste_management.aspx">Sembcorp</a>).
 +
</div>
  
<br><br>
 
  
<h3></h3>
+
</td>
 +
</tr>
 +
 
 +
<! ------P4----->
 +
<tr id = "p4"><td><br></td></tr>
 +
 
 +
<tr><td style = "font-size:20px;padding-bottom:10px;"><a><b>
 +
Safety Requirements for iGEM Participation
 +
</b></a></td></tr>
 +
 
 +
<tr style = "border-top:2px solid grey;">
 +
<td style="padding-bottom:30px;padding-top:30px;padding-left:60px;padding-right:60px">
 +
 
 +
<div style = "text-align:justify;font-size:14px">
 +
For the fulfillment of requirements for safety from the iGEM foundation, we have submitted the <a href = "https://2015.igem.org/Safety/About_Our_Lab?team_id=1804">About Our Lab</a> safety forms and the <a href = "https://2015.igem.org/Safety/Final_Safety_Form?team_id=1804">Final Safety</a> form.
 +
<br><br>
 +
We have also performed a <a href = "https://2015.igem.org/Safety/Check_In">check-in</a> for the <a href = "http://parts.igem.org/wiki/index.php?title=Part:BBa_K299812" style = "text-decoration:none">Biobricks Part Bba_k299812</a>, which contains the invasin gene from Yersinia pseudotuberculosis and the listerolysin O gene from Listeria monocytogenes.
 +
</div>
  
 
</td>
 
</td>
 
</tr>
 
</tr>
 +
  
  
 
</table>
 
</table>
 +
 
</center>
 
</center>
<!------------------------------------------------------ Team End ---------------------------------------------------->
 
  
  
 +
 +
<!------------------------------------------------------ Entry End ---------------------------------------------------->
  
  
 
</div>
 
</div>
 
</td></tr></table>
 
</td></tr></table>
 +
  
 
<! ------------------------------- Main Content END --------------------------------------------->
 
<! ------------------------------- Main Content END --------------------------------------------->
  
 
<! ------------------------------- Footer START ------------------------------------------------>
 
<! ------------------------------- Footer START ------------------------------------------------>
 +
  
 
<div id="footer1">
 
<div id="footer1">
Line 162: Line 272:
 
<div class="left_sec">
 
<div class="left_sec">
 
<p>
 
<p>
<img src = "https://static.igem.org/mediawiki/2015/a/ab/SPSingapore_Team-Logo-New.png" height = "80px">
+
<img src = "https://static.igem.org/mediawiki/2015/a/ab/SPSingapore_Team-Logo-New.png" height = "60px" style="margin-top:5px;margin-left:-130px;">
 
</p>
 
</p>
 
</div>
 
</div>
 
<div class="right_sec">
 
<div class="right_sec">
 
<p>
 
<p>
<img src = "https://static.igem.org/mediawiki/2015/0/05/SPSingapore_NUS-Logo.png" height = "60px" style = "margin-top:10px;margin-right:30px;padding-right:30px;border-right: 3px solid lightgrey;">
+
<img src="https://static.igem.org/mediawiki/2015/0/05/SPSingapore_NUS-Logo.png" height="50px" style="margin-top:10px;margin-right:30px;padding-right:30px;border-right: 3px solid lightgrey;">
<img src = "https://static.igem.org/mediawiki/2015/7/72/SPSingapore_SPS-Logo.png" height = "60px" style = "margin-top:10px;margin-right:50px;"></a>
+
<img src="https://static.igem.org/mediawiki/2015/7/72/SPSingapore_SPS-Logo.png" height="50px" style="margin-top:10px;margin-right:30px;">
 
</p>
 
</p>
 
</div>
 
</div>

Latest revision as of 23:12, 18 September 2015


Safety



Safety is always of paramount importance in the laboratory, even more so when biological agents are involved. Our team takes safety very seriously and have worked hard to ensure that our procedures are up to scratch.

Biosafety in our project involves minimising the risks to the researchers working in the laboratory, as well as the general public in future medical applications based off our research.

We are proud that SPS Wet Lab has obtained an 'A' grade for the FOS Housekeeping Inspection 2015 for lab safety over the summer of 2015 and strive to maintain a safe working environment for all researchers in the lab.


Safety in Handling Biological Organisms
Non-pathogenic strains of E. coli K-12 strains BL21 and dH5α from Life Technologies were used for bacterial cloning of plasmids and expression of proteins of interest. These strains are Risk group 1 and were handled in a BSL2 Biosafety cabinet. The E. coli strain carrying the Biobrick BBaK299812 (containing parts derived from Risk group 2 organisms) was handled as a Risk Group 2 agent. Mammalian cell line HepG2 is classified under Risk group 2, and was also cultured in a BSL2 Biosafety cabinet.

Safety in Project Design
In our project, we aim to engineer non-pathogenic E. coli as a vector to deliver a potential drug into the tumour core. We use the Biobricks Part BBa_K299812, which contains the invasin gene from Yersinia pseudotuberculosis and the listerolysin O gene from Listeria monocytogenes. The Invasin protein allows for bacteria to enter mammalian cells, while Listerolysin O is a pore-forming protein that enable bacteria to escape the endosome. These two proteins are involved in pathogenesis of their respective bacterial species.

The Invasin and Listerolysin proteins enable our E. coli to enter mammalian cells, and escape the endosome, where they can subsequently deliver an encoded therapeutic to kill the tumour cell. To ensure that these proteins are only expressed under the conditions of the tumour microenvironment, the invasin and listerolysin proteins will be placed under the control of an anaerobic promoter, and a quorum sensing system.

Safety in Our Lab
All our team members have undergone Chemical, Biological and Fire Safety Training from the Office of Safety, Health and Environment (OSHE) , the department in charge of Laboratory and Work Safety at the National University of Singapore.

For each protocol used for our experiments, we have a separate risk assessment. Please refer to our ‘protocols’ page for more information.

Our laboratory is equipped with biological and chemical spill kits, and all members of our iGEM Team are trained to handle Biological and Chemical Spills. Our laboratory is classified as Biosafety Level 2, according to the classification by the World Health Organisation (WHO) and the Genetic Modification Advisory Committee of the government of Singapore.

Bacterial work and Mammalian cell culture are performed in separate BSL2 Biosafety Cabinets, while DNA work is done on the bench. No cytotoxic reagents are used in our laboratory; Sybr Safe DNA stain is used rather than Ethidium Bromide. Liquid biological waste is decontaminated using 10% Bleach, while Solid biological waste is sent for incineration in a local incineration plant devoted to medical waste (Sembcorp).

Safety Requirements for iGEM Participation
For the fulfillment of requirements for safety from the iGEM foundation, we have submitted the About Our Lab safety forms and the Final Safety form.

We have also performed a check-in for the Biobricks Part Bba_k299812, which contains the invasin gene from Yersinia pseudotuberculosis and the listerolysin O gene from Listeria monocytogenes.