Team:Wisconsin-Madison/safety
From 2011.igem.org
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<a href="https://2011.igem.org/Team:Wisconsin-Madison">Main</a> | <a href="https://2011.igem.org/Team:Wisconsin-Madison">Main</a> | ||
<a href="https://2011.igem.org/Team:Wisconsin-Madison/whatisigem">What is iGEM?</a> | <a href="https://2011.igem.org/Team:Wisconsin-Madison/whatisigem">What is iGEM?</a> | ||
+ | <a href="https://2011.igem.org/Team:Wisconsin-Madison/ca">Contributions & Attributions</a> | ||
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<a href="https://2011.igem.org/Team:Wisconsin-Madison/protocols">Protocols</a> | <a href="https://2011.igem.org/Team:Wisconsin-Madison/protocols">Protocols</a> | ||
- | <a href="https://2011.igem.org/Team:Wisconsin-Madison/calender"> | + | <a href="https://2011.igem.org/Team:Wisconsin-Madison/calender">Calender</a> |
<a href="https://2011.igem.org/Team:Wisconsin-Madison/references">References</a> | <a href="https://2011.igem.org/Team:Wisconsin-Madison/references">References</a> | ||
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<i>What Safety Concerns Exist for Our Project?</i><br> | <i>What Safety Concerns Exist for Our Project?</i><br> | ||
The safety concerns for our project can be separated into two categories: the immediate concerns for our lab and researchers, and the concerns for public safety and environment if this organism gets widespread use. | The safety concerns for our project can be separated into two categories: the immediate concerns for our lab and researchers, and the concerns for public safety and environment if this organism gets widespread use. | ||
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Our project uses the DH10B strain of E. Coli, which has been specifically engineered for lab use for the propagation of large insert DNA clones [1]. DH10B is a very safe organism and is classified as a Biosafety Level 1 (BSL1) organism. All researchers were trained in the proper chemical and biological safety techniques, as is required per the Center for Disease Control (CDC) and National Institute of Health (NIH) guidelines. Adherence to these guidelines (proper lab attire, handling techniques, etc.) was maintained. Lab personnel were also given proper training on all lab equipment prior to use. Researchers were informed of the dangers of all the chemicals (Ethydium Bromide) used. Experiments required no further safety measures other than those specified in the BSL1 guidelines. | Our project uses the DH10B strain of E. Coli, which has been specifically engineered for lab use for the propagation of large insert DNA clones [1]. DH10B is a very safe organism and is classified as a Biosafety Level 1 (BSL1) organism. All researchers were trained in the proper chemical and biological safety techniques, as is required per the Center for Disease Control (CDC) and National Institute of Health (NIH) guidelines. Adherence to these guidelines (proper lab attire, handling techniques, etc.) was maintained. Lab personnel were also given proper training on all lab equipment prior to use. Researchers were informed of the dangers of all the chemicals (Ethydium Bromide) used. Experiments required no further safety measures other than those specified in the BSL1 guidelines. | ||
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Our host strain (DH10B) was probably the most important factor regarding safety concerns for the environment and the public well-being. As previously mentioned, this E.Coli strain has been engineered for lab use due to its properties of high DNA transformation efficiency and the maintenance of large plasmids. Wild type strains of E.Coli would quickly outcompete DH10B in the event of human or environmental exposure. Initial experiments also seem to indicate that our sensing system strains the metabolism/homeostasis of our DH10B, further reducing its viability both inside and outside the lab environment. Additionally, the plasmids introduced into the DH10B strain do not contain any antibiotic resistances not commonly used for synthetic biology selectivity or otherwise improve the resistance, durability, or reproduction of our organism that would give it unique advantages/characteristics over its native brethren. If ever used in industry, our organism does not require any human or environmental exposure to be effective. It is intended solely for use in controlled environments (i.e. labs, feed reactors, etc.). The ethical implications for our organism are also considered. | Our host strain (DH10B) was probably the most important factor regarding safety concerns for the environment and the public well-being. As previously mentioned, this E.Coli strain has been engineered for lab use due to its properties of high DNA transformation efficiency and the maintenance of large plasmids. Wild type strains of E.Coli would quickly outcompete DH10B in the event of human or environmental exposure. Initial experiments also seem to indicate that our sensing system strains the metabolism/homeostasis of our DH10B, further reducing its viability both inside and outside the lab environment. Additionally, the plasmids introduced into the DH10B strain do not contain any antibiotic resistances not commonly used for synthetic biology selectivity or otherwise improve the resistance, durability, or reproduction of our organism that would give it unique advantages/characteristics over its native brethren. If ever used in industry, our organism does not require any human or environmental exposure to be effective. It is intended solely for use in controlled environments (i.e. labs, feed reactors, etc.). The ethical implications for our organism are also considered. | ||
<p><br> | <p><br> |
Latest revision as of 23:13, 28 September 2011
Safety Q&A
Would any of your project ideas raise safety issues in terms of: researcher safety, public safety, or environmental safety?
Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues? If yes, did you document these issues in the Registry? How did you manage to handle the safety issue? How could other teams learn from your experience? Is there a local biosafety group, committee, or review board at your institution? What do they think of your project? The Office of Biological Safety (OBS) in the Department of Environment, Health, and Safety at the UW-Madison runs a biological safety course which was mandatory for all iGEM participants. Beyond adhering to all guidelines established in this, we have not further discussed project specifics with the OBS. Do you have any other ideas how to deal with safety issues that could be useful for future iGEM competitions? How could parts, devices and systems be made even safer through biosafety engineering? Maintaining best practices established by biosafety committees is always useful, but there are even more interesting options that could be useful for broader synthetic biology safety down the road. For example, making engineered organisms dependent on non-standard nucleotides or amino acids which are only provided in a laboratory setting could help prevent the accidental release of recombinant organisms.
"The attitudes and actions of those who work in the laboratory determine their own safety, and that of their colleagues and of the community. Laboratory equipment and design can contribute to safety only if they are used properly by people who are genuinely concerned and knowledgeable about safety issues."
Why Care About Safety?
What Safety Concerns Exist For Synthetic Biology?
What Safety Concerns Exist for Our Project? Our project uses the DH10B strain of E. Coli, which has been specifically engineered for lab use for the propagation of large insert DNA clones [1]. DH10B is a very safe organism and is classified as a Biosafety Level 1 (BSL1) organism. All researchers were trained in the proper chemical and biological safety techniques, as is required per the Center for Disease Control (CDC) and National Institute of Health (NIH) guidelines. Adherence to these guidelines (proper lab attire, handling techniques, etc.) was maintained. Lab personnel were also given proper training on all lab equipment prior to use. Researchers were informed of the dangers of all the chemicals (Ethydium Bromide) used. Experiments required no further safety measures other than those specified in the BSL1 guidelines. Our host strain (DH10B) was probably the most important factor regarding safety concerns for the environment and the public well-being. As previously mentioned, this E.Coli strain has been engineered for lab use due to its properties of high DNA transformation efficiency and the maintenance of large plasmids. Wild type strains of E.Coli would quickly outcompete DH10B in the event of human or environmental exposure. Initial experiments also seem to indicate that our sensing system strains the metabolism/homeostasis of our DH10B, further reducing its viability both inside and outside the lab environment. Additionally, the plasmids introduced into the DH10B strain do not contain any antibiotic resistances not commonly used for synthetic biology selectivity or otherwise improve the resistance, durability, or reproduction of our organism that would give it unique advantages/characteristics over its native brethren. If ever used in industry, our organism does not require any human or environmental exposure to be effective. It is intended solely for use in controlled environments (i.e. labs, feed reactors, etc.). The ethical implications for our organism are also considered.
a. Risks to the safety and health of team members or others in the lab?
b. Risks to the safety and health of the general public if released by
design or accident?
c. Risks to environmental quality if released by design or accident?
d. Risks to security through malicious misuse by individuals, groups or states?
Under what biosafety provisions will / do you operate?
Does your institution have its own biosafety rules and if so what are they?
Provide a link to them online if possible.
Does your institution have an Institutional Biosafety Committee or equivalent group? If yes, have you discussed your project with them?
Describe any concerns or changes that were made based on this review.
Does your country have national biosafety regulations or guidelines? If so, provide a link to them online if possible.
Do you have other ideas on how to deal with safety or security issues that could be useful for future iGEM
competitions? How could parts, devices and systems be made even safer through biosafety engineering?
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