Team:ULB-Brussels/Human
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- | <p>However, we realized that few people were aware of it, and still mingled GMM with | + | <p>However, we realized that few people were aware of it, and still mingled GMM with genetically modified crops, which have a really bad reputation in western Europe. Although, $\MyColi$ would be welcomed in the industry, we feared that if for some reason we had to ask the authorization of the public to use $\MyColi$, we would only face fear, incomprehension, and eventually refusal. Since the use of synthetical organisms is an important ethical and societal issue, we think that the general public should be included in the debate. But we also think that it should be properly informed about the nature of synthetic organism and the way they are used. Hence, we decided to organize several popularization events on the subject. |
<!-- Since we firmly believe that the use of GMOs is an important : Hey, faites gaffe!!! --> | <!-- Since we firmly believe that the use of GMOs is an important : Hey, faites gaffe!!! --> | ||
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- | <p>After discussion within the team and with our friends and families, we | + | <p>After discussion within the team and with our friends and families, we decided that the themes of our popularization events would be the synthetic biology, the use of GMMs in research and industry (and the role that $\MyColi$ could play in it), and the means and perspectives of genetic manipulations. |
<!-- the difference between GMMs and agricultural GMOs, and, given the opportunity, we would also discuss the pros and cons of agricultural GMOs, even if it is a bit off topic for $\MyColi$. | <!-- the difference between GMMs and agricultural GMOs, and, given the opportunity, we would also discuss the pros and cons of agricultural GMOs, even if it is a bit off topic for $\MyColi$. | ||
--></p> | --></p> | ||
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As mentioned earlier, the main concerns raised by $\MyColi$ depend more on the protein that we chose to produce than on $\MyColi$ in itself. However, $\MyColi$ could compel an escaped recombinant bacterium to produce an industrial protein in the environment, when a bacterium without the $\MyColi$ system would quickly degenerate to stop producing the protein of industrial interest. The risk seems thin, since such an overproducing bacterium would suffer from a clear competitive disadvantage in a wild environment. However it is not excluded that the plasmid containing the $\MyColi$ system, since it benefits from the proprieties of the TA System, could manage to maintain itself anyway through Horizontal Gene transfer (HGT), at the expend of the wild bacteria it infects.</p> | As mentioned earlier, the main concerns raised by $\MyColi$ depend more on the protein that we chose to produce than on $\MyColi$ in itself. However, $\MyColi$ could compel an escaped recombinant bacterium to produce an industrial protein in the environment, when a bacterium without the $\MyColi$ system would quickly degenerate to stop producing the protein of industrial interest. The risk seems thin, since such an overproducing bacterium would suffer from a clear competitive disadvantage in a wild environment. However it is not excluded that the plasmid containing the $\MyColi$ system, since it benefits from the proprieties of the TA System, could manage to maintain itself anyway through Horizontal Gene transfer (HGT), at the expend of the wild bacteria it infects.</p> | ||
- | In the current state of our project, the protein production is boosted thanks to the TA System, but the plasmids are maintained through the usual system of antibiotic resistance, since the toxin and the antitoxin | + | In the current state of our project, however, the protein production is boosted thanks to the TA System, but the plasmids are maintained through the usual system of antibiotic resistance, since the toxin and the antitoxin are placed on different plasmids bearing different resistance genes. The system will thus decay quickly if the $\MyColi$ bacteria wander in a wild environment, without any antibiotic. |
- | If, for one reason or another, the overproduction of a protein did not | + | Furthermore, in the final version of our project (that is, if we have the time to go this far), the toxin gene will be inserted in the genomic DNA of the bacteria, preventing it to ever be lost, and compelling the bacteria to keep the plasmid bearing the genes of the antitoxin and the protein of interest. It will also prevent any reasonable chance of Horizontal Gene Transfer of the $\MyColi$ system as a whole.</p> |
+ | If, for one reason or another, the overproduction of a protein did not result in a competitive disadvantage, the inducible promoter of the antitoxin would act as a built-in biocontainment device. Indeed,if one selects in the bioreactor an artificial inducer (that is, an inducer not found in nature) for the antitoxin, the escaped bacteria would have no means to inhibit the toxin and would quickly die outside of the bioreactor. | ||
<!-- A VERIFIER, pas de référence ? : Several of containment devices have been developed by IGEM teams, and other are already in use in the industry. --> | <!-- A VERIFIER, pas de référence ? : Several of containment devices have been developed by IGEM teams, and other are already in use in the industry. --> | ||
</p> | </p> | ||
- | In conclusion, $\MyColi$ seems to be a safe and predictable system, whose biggest danger would be to be used to produce a dangerous protein. This latter problem has to be addressed on a case-by-case basis, by other | + | In conclusion, $\MyColi$ seems to be a safe and predictable system, whose biggest danger would be to be used to produce a dangerous protein. This latter problem has to be addressed on a case-by-case basis, by other institutions than ours. |
</p> | </p> | ||
We have a safety page <a href="https://2014.igem.org/Team:ULB-Brussels/Safety"><b> here </b></a> too.</p> | We have a safety page <a href="https://2014.igem.org/Team:ULB-Brussels/Safety"><b> here </b></a> too.</p> |
Revision as of 18:23, 29 September 2014
$~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\MyColi}{{\small Mighty\hspace{0.12cm}Coli}} \newcommand{\Stabi}{\small Stabi}$ $\newcommand{\EColi}{\small E.coli} \newcommand{\SCere}{\small S.cerevisae}\\[0cm] ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\PI}{\small PI}$ $\newcommand{\Igo}{\Large\mathcal{I}} \newcommand{\Tgo}{\Large\mathcal{T}} \newcommand{\Ogo}{\Large\mathcal{O}} ~$
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