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Team:Tuebingen/Safety
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| + | = Safety = | ||
| + | ''Would any of your project ideas raise safety issues in terms of: researcher safety, public safety, or environmental safety?''<br /> | ||
| - | + | <blockquote>All our work is supervised by PhD students, PhDs and professors of our university who are very experienced in lab work and are currently working in genetics. We document our work in our lab notebook to enable replicability and prevent unnecessary errors. In the case of an error, we are able to locate its source and correct it next time. | |
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Our project does not pose any dangers to researchers or the public: We are following widely used lab protocols in a appropriate lab facility. The organisms used in our project, namely ''E. coli'' (TOP10 strain) and ''S. cerevisiae'', are well-known and considered safe. | Our project does not pose any dangers to researchers or the public: We are following widely used lab protocols in a appropriate lab facility. The organisms used in our project, namely ''E. coli'' (TOP10 strain) and ''S. cerevisiae'', are well-known and considered safe. | ||
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Although, by building a biosensor we are tackling an environmental problem, our system is not intended to be used in the field but in a lab only. Clients of our system are supposed to take samples from close waters, such as rivers and seas, and apply our modified yeast strain to it. | Although, by building a biosensor we are tackling an environmental problem, our system is not intended to be used in the field but in a lab only. Clients of our system are supposed to take samples from close waters, such as rivers and seas, and apply our modified yeast strain to it. | ||
| - | According to our laboratory we work at a so called | + | According to our laboratory we work at a so called ''S1-Sicherheitslabor'', which implies several methods for guaranteeing safety to researchers and environment. |
| - | + | </blockquote> | |
| + | ''Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues?''<br /> | ||
| + | <blockquote> | ||
| + | We have designed 3 different types of BioBricks. Membrane bound receptors for sensing hormones, a small inverter system to regulate our reporter gene. None of these are found toxic or dangerous by any means. | ||
| + | The receptors we use are synthesized after genome-sequences of ''Danio rerio'' and ''Xenopus laevis'', both are commonly used model organisms. The rest of the genes and promoters are extracted from the ''Saccharomyces cerevisiae'' genome via PCR. All of the parts we use are expressed in wildtype organisms and not known to have any harmful effect on humans or other organisms. | ||
| + | </blockquote> | ||
| - | + | ''Which specific biosafety rules or guidelines do you have to consider in your country?''<br /> | |
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| - | + | <blockquote> | |
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In Germany any work with genetically modified organisms is regulated by the "Gentechnikgesetz". There are different biosafety levels reaching from 1 to 4. Our lab has been registered as level 1. | In Germany any work with genetically modified organisms is regulated by the "Gentechnikgesetz". There are different biosafety levels reaching from 1 to 4. Our lab has been registered as level 1. | ||
Our work matches the definition of level 1 since on our current understanding we see no threats on human health or the environment. | Our work matches the definition of level 1 since on our current understanding we see no threats on human health or the environment. | ||
| - | Genetically modified organisms are allowed to be released into nature only on permission of the Umweltministerium and once freed need to be constantly monitored. | + | Genetically modified organisms are allowed to be released into nature only on permission of the Umweltministerium and once freed they need to be constantly monitored. |
| - | + | </blockquote> | |
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| + | ''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?''<br /> | ||
| - | < | + | <blockquote> |
| - | + | Parts that are able to induce apoptosis or autolyis could be expressed under promoters that are activated if a specific substance is lacking or present in an uncontrolled environment as opposed to a lab. As an example the team of UCL London had a concept for autolysis that could be of value in [https://2011.igem.org/Team:UCL_London/Research/Extractery/Theory 2011]. A possible promoter could be induced by the lack of iron, which then would have to be a part of the culture medium in the lab. In environments without iron the organism not only couldn't survive but would be killed immediately. A mechanism of this kind would then have to be a obligatory requirement for all contest-submissions. | |
| - | Parts that are able to induce apoptosis or autolyis could be expressed under promoters that are activated if a specific substance is lacking or present in an uncontrolled environment as opposed to a lab. As an example the team of UCL London had a concept for autolysis that could be of value in [https://2011.igem.org/Team:UCL_London/Research/Extractery/Theory 2011]. A possible promoter could be induced by the lack of iron, which then would have to be a part of the culture medium in the lab. In environments without iron the organism not only couldn't survive but would be killed immediately. A mechanism of this kind would then have to be a obligatory requirement for all contest-submissions. | + | </blockquote> |
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Latest revision as of 13:17, 26 September 2012
Safety
Would any of your project ideas raise safety issues in terms of: researcher safety, public safety, or environmental safety?
All our work is supervised by PhD students, PhDs and professors of our university who are very experienced in lab work and are currently working in genetics. We document our work in our lab notebook to enable replicability and prevent unnecessary errors. In the case of an error, we are able to locate its source and correct it next time. Our project does not pose any dangers to researchers or the public: We are following widely used lab protocols in a appropriate lab facility. The organisms used in our project, namely E. coli (TOP10 strain) and S. cerevisiae, are well-known and considered safe. Although, by building a biosensor we are tackling an environmental problem, our system is not intended to be used in the field but in a lab only. Clients of our system are supposed to take samples from close waters, such as rivers and seas, and apply our modified yeast strain to it. According to our laboratory we work at a so called S1-Sicherheitslabor, which implies several methods for guaranteeing safety to researchers and environment.
Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues?
We have designed 3 different types of BioBricks. Membrane bound receptors for sensing hormones, a small inverter system to regulate our reporter gene. None of these are found toxic or dangerous by any means. The receptors we use are synthesized after genome-sequences of Danio rerio and Xenopus laevis, both are commonly used model organisms. The rest of the genes and promoters are extracted from the Saccharomyces cerevisiae genome via PCR. All of the parts we use are expressed in wildtype organisms and not known to have any harmful effect on humans or other organisms.
Which specific biosafety rules or guidelines do you have to consider in your country?
In Germany any work with genetically modified organisms is regulated by the "Gentechnikgesetz". There are different biosafety levels reaching from 1 to 4. Our lab has been registered as level 1. Our work matches the definition of level 1 since on our current understanding we see no threats on human health or the environment. Genetically modified organisms are allowed to be released into nature only on permission of the Umweltministerium and once freed they need to be constantly monitored.
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?
Parts that are able to induce apoptosis or autolyis could be expressed under promoters that are activated if a specific substance is lacking or present in an uncontrolled environment as opposed to a lab. As an example the team of UCL London had a concept for autolysis that could be of value in 2011. A possible promoter could be induced by the lack of iron, which then would have to be a part of the culture medium in the lab. In environments without iron the organism not only couldn't survive but would be killed immediately. A mechanism of this kind would then have to be a obligatory requirement for all contest-submissions.
