Team:Lethbridge/Safety
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===<font color="white">Researcher Safety=== | ===<font color="white">Researcher Safety=== | ||
- | The | + | The Lethbridge team project uses <i>Escherichia coli</i> bacteria, particularly the strains BL21 (DE3) and DH5α. These strains are the most widely used bacteria in biotechnology, biological and biochemistry research due to their lack of pathogenicity. These strains of bacteria are also very useful and possess many unique qualities that make them ideal for recombinant DNA experiments such as transformations and protein over expressions. These experiments are the foundation for the majority of the projects in the iGEM competition and are one of the main reasons why these particular <i>E. coli</i> strains are used preferentially by a large proportion of laboratories around the world. This means that at no point in time will any experimenters be exposed to pathogens. |
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==<font color="white">Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues?== | ==<font color="white">Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues?== | ||
- | The <html><a href="https://2010.igem.org/Team:Lethbridge/Parts"><font color="green"> BioBrick components that the 2010 | + | The <html><a href="https://2010.igem.org/Team:Lethbridge/Parts"><font color="green"> BioBrick components that the 2010 Lethbridge iGEM team has made</font></a></html> do not raise any immediate safety issues. However, as a team, we have examined possible future consequences that could arise from the improper use of any portion of our submitted parts. The <html><a href="https://2010.igem.org/Team:Lethbridge/Project/Magnetic_Nanoparticles"><font color="green"> <i>Mms6</i></font></a></html> gene could be used to generate toxic magnetic nanoparticles that if found in a high enough concentration could potentially pose a risk, especially if ingested. Although the gene, <html><a href="https://2010.igem.org/Team:Lethbridge/Project/Catechol_Degradation"><font color="green"> <i>xylE</i>, <font color="white">is not particularly harmful on its own, the chemical compound, <font color="green">catechol, that the <i>xylE</i> protein catechol-2,3-dioxygenase</font></a></html> is responsible for breaking down, can be poisonous upon ingestion and therefore appropriate safety measures should be taken. Finally, the <html><a href="https://2010.igem.org/Team:Lethbridge/Project/Compartamentalization"><font color="green">microcompartments made from the lumazine synthase gene</font></a></html>, could serve as potential storage vesicles for agents of biological warfare. Even though, no safety issues directly related to our BioBrick parts were evident this year, it is important to consider what future teams or individuals may discover. |
==<font color="white">Local Biosafety Regulations== | ==<font color="white">Local Biosafety Regulations== | ||
- | At the University of Lethbridge, the <html><a href="http://www.uleth.ca/hum/riskandsafetyservices/" target="new"><font color="green"> Risk and Safety Services department</font></a></html> has appointed a committee devoted to biosafety. This university committee ensures that biological materials are used safely on campus and foresee no problems with the | + | At the University of Lethbridge, the <html><a href="http://www.uleth.ca/hum/riskandsafetyservices/" target="new"><font color="green"> Risk and Safety Services department</font></a></html> has appointed a committee devoted to biosafety. This university committee ensures that biological materials are used safely on campus and foresee no problems with the Lethbridge 2010 iGEM team’s project, as long as the proper safety practices in the laboratory are employed. |
==<font color="white">Canadian Biosafety Regulations== | ==<font color="white">Canadian Biosafety Regulations== | ||
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==<font color="white">How could parts, devices and systems be made even safer through biosafety engineering?</font>== | ==<font color="white">How could parts, devices and systems be made even safer through biosafety engineering?</font>== | ||
- | As previously mentioned, the 2010 | + | As previously mentioned, the 2010 Lethbridge iGEM team has proposed the incorporation of the<html><a href="https://2010.igem.org/Team:Lethbridge/Project/DNA_Degradation"><font color="green"> <i>BamHI</i></font></a></html> gene into its constructs, which would allow for degradation of the bacterial genomic material, upon release into the tailings ponds environment. In general, in order to make biological engineering safer, having control over the growth of the system could be accomplished through the careful planning and design of the parts and devices that comprise them. This could be established by having bacteria incorporate a plasmid that can be triggered to translate a toxin. By choosing these toxins to be endonucleases, scientists can destroy the genetic material within their bacteria and therefore prevent future replication. |
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