Team:ULB-Brussels/Safety

From 2014.igem.org

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deep attention is taken to use safely our lab equipement and our E.Coli bacteria. </p></section>
deep attention is taken to use safely our lab equipement and our E.Coli bacteria. </p></section>
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We use only benign genes and strains of microorganisms (E. Coli K-12, M.C. 1061, S. Cervesiae,...) and the toxins we use are of no danger for humans. </p>
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We use only benign genes and strains of microorganisms (E. Coli K-12, M.C. 1061, S. Cervesiae,...) </p>
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Furthermore,once our project will be finished, any bacterium that might escape</p>
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and the toxins that we use aren't dangerous by contact to humans. </p>
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will quickly die. Indeed, the antitoxin production is subordinate to an arabinose-dependant promoter. Thus,</p>
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Furthermore, once our project will be finished, any bacteria escaped will quickly die. </p>
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Indeed, the antitoxin production is subordinate to an arabinose-dependant promoter. Thus,</p>
if it escapes the lab, the bacterium will no longer be provided with the inducer, and it will stop producing the antitoxin. </p></section>
if it escapes the lab, the bacterium will no longer be provided with the inducer, and it will stop producing the antitoxin. </p></section>

Revision as of 15:32, 3 August 2014

$~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\MyColi}{{\small Mighty\hspace{0.12cm}Coli}} \newcommand{\Stabi}{\small Stabi}$ $\newcommand{\EColi}{\small E.coli} \newcommand{\SCere}{\small S.cerevisae}\\[0cm] ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\PI}{\small PI}$ $\newcommand{\Igo}{\Large\mathcal{I}} \newcommand{\Tgo}{\Large\mathcal{T}} \newcommand{\Ogo}{\Large\mathcal{O}} ~$ Example of a hierarchical menu in CSS

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- Université Libre de Bruxelles -



Safety


To avoid an eventual contamination and apply the emergency mesures in the lab,

deep attention is taken to use safely our lab equipement and our E.Coli bacteria.

We use only benign genes and strains of microorganisms (E. Coli K-12, M.C. 1061, S. Cervesiae,...)

and the toxins that we use aren't dangerous by contact to humans.

Furthermore, once our project will be finished, any bacteria escaped will quickly die.

Indeed, the antitoxin production is subordinate to an arabinose-dependant promoter. Thus,

if it escapes the lab, the bacterium will no longer be provided with the inducer, and it will stop producing the antitoxin.

At last, Mighty Coli should ultimately be used in closed bioreactors, which also have their own built-in biocontainment component.

We can thus safely assume that the Mighty Coli project does not comprehend any appreciable risk.

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