Team:LMU-Munich/Laboratory Safety

From 2012.igem.org

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==Lab and Project Safety==
==Lab and Project Safety==
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For iGEM 2012, teams are asked to detail how they approached any issues of biological safety associated with their projects. Specifically, teams should consider the following <b>questions</b>:
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Here you find our considerations on the following topics of biological safety for our project:  
<b> 1) Would any of your project ideas raise safety issues in terms of:</b>
<b> 1) Would any of your project ideas raise safety issues in terms of:</b>
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* <b>a)  </b>researcher safety,
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* <b>a)  </b>researcher safety?
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* <b>b)  </b>public safety, or
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* <b>b)  </b>public safety?
* <b>c)  </b>environmental safety?
* <b>c)  </b>environmental safety?
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To assure safe working practice throughout the competition, every team member participated in a general safety meeting regarding good laboratory practice and working with genetically modified organisms (GMOs), including storage and disposal. We work only with non-hazardous, non-pathogenic organisms like <i>Escherichia coli </i>(lab strain XL1 blue) and <i>Bacillus subtilis </i> (W168). We follow the safety regulations that apply for the [http://en.wikipedia.org/wiki/Biosafety_level#Biosafety_level_1 biological safety level 1] classification.  That means we wear a lab coat and single-use gloves. When working with hazardous chemicals (e.g. liquid N<sub>2</sub>) we wear goggles as well. Furthermore, dangerous substances are stored and handled in designated rooms in order to assure the safety of the researchers.
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To assure safe working practice throughout the competition, every team member participated in a general safety meeting regarding good laboratory practice and working with genetically modified organisms (GMOs), including storage and disposal. We work only with non-hazardous, non-pathogenic organisms like <i>Escherichia coli </i>(lab strain XL1 blue) and <i>Bacillus subtilis </i> (W168). We follow the safety regulations that apply for the [http://en.wikipedia.org/wiki/Biosafety_level#Biosafety_level_1 biological safety level 1] classification.  That means we wear lab coats and single-use gloves. When working with hazardous chemicals (e.g. liquid N<sub>2</sub>) we wear goggles as well. Furthermore, dangerous substances are stored and handled in designated rooms in order to assure the safety of the researchers.
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The other subproject, [[Team:LMU-Munich/Spore_Coat_Proteins|'''Sporo'''bead]] involves potentially the creation of GMOs and could have unknown effects to the public or the environment. Although we have great plans for the use of our Sporobeads, they never leave our laboratory, so they cannot harm the public or environment. For possible future applications, we try to block the germination of our '''Sporo'''beads in two different ways ([[Team:LMU-Munich/Germination_Stop|'''Germination'''Stop]]), so that they cannot proliferate. This is our approach towards the safety of our Sporobeads.
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The other subproject, [[Team:LMU-Munich/Spore_Coat_Proteins|'''Sporo'''bead]] involves the creation of GMOs which have unknown effects to the public or the environment. Although we have great plans for the use of our Sporo'''beads''', they never leave our laboratory, so they cannot harm the public or environment. For possible future applications, we will prevent the germination of our '''Sporo'''beads in two different ways ([[Team:LMU-Munich/Germination_Stop|'''Germination'''Stop]]), so that they cannot proliferate. This is our approach towards the safety of our Sporo'''beads'''.
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We have not worked on it yet, but there also is the possibility to remove antibiotic resitance genes from the ''Bacillus subtilis'' genome (for example with [https://static.igem.org/mediawiki/2012/6/6d/LMU-Munich_2012_Clean_deletions_in_Bacillus_subtilis.pdf pMAD], a vector that we used to delete genes in ''B. subtilis''). All our constructs are used while being integrated into the genome. Therefore all resistances could be removed (without removing the functional constructs) before the use of the Sporobeads. Thereby any pathogens would not have the possibility to grab resistance genes from our strains.
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We have not worked on it yet, but there also is the possibility to remove antibiotic resitance genes from the ''Bacillus subtilis'' genome (for example with [https://static.igem.org/mediawiki/2012/6/6d/LMU-Munich_2012_Clean_deletions_in_Bacillus_subtilis.pdf pMAD], a vector that we used to delete genes in ''B. subtilis''). All of our constructs are used while being integrated into the genome. Therefore all resistances could be removed (without removing the functional constructs) before the use of the Sporo'''beads'''. Other pathogens would thereby not have the possibility to grab resistance genes from our strains.
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From the best of our knowledge the parts, strains or spores we use do not raise any safety concerns. However a point that needs to be discussed here is the potential '''risk of misusing our spores'''. We offer an easy platform for displaying any protein of interest. Could this platform be used by e.g. a bio-terrorist? Since all information on how to build a spore with a protein of interest is given on this website one could imagine to use '''Sporo'''beads as a vehicle for lethal proteins. Our team is aware of this potential risk. However, our spores can not germinate, so the risk of a rapidly spreading epidemic is negligible. Today it still seems "easier" to use directly know pathogens like e.g. ''Helicobacter pylori''.
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From the best of our knowledge, the parts, strains and spores we use do not raise any safety concerns. However a point that needs to be discussed here is the potential '''risk of misusing our spores'''. We offer an easy platform for displaying any protein of interest on our spores. Could this platform be used by e.g. a bio-terrorist? Since all information on how to build a spore with a protein of interest is given on this website, one could imagine to use '''Sporo'''beads as a vehicle for lethal proteins. Our team is aware of this potential risk. However, our spores can not germinate, so the risk of a rapidly spreading epidemic is negligible. Today it still seems "easier" to use directly know pathogens like e.g. ''Helicobacter pylori''.
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Our biobricks contain promotors, regulators, a bacterial toxine and reporter genes. None of them are able to cause illnesses or threaten humans in any other way. All inserts are also derived from non-pathogenic, non-hazardous organisms. The amplified and cloned fragments again belong to the GMO safety class S1.
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Our Biobricks contain promotors, regulators, a bacterial toxin and reporter genes. None of them are able to cause illnesses or threaten humans in any other way. All inserts are also derived from non-pathogenic, non-hazardous organisms. The amplified and cloned fragments again belong to the GMO safety class S1.
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We did an interview with the safety Commissioner Dr. Schubar who is responsible for our university. He confirmed that we are working with a safe strain (''B. subtilis'' W168 which has a tryptophan auxotrophy) and are only using safe plasmids, genes and promoters. He is not in a position to allow the release of our spores, but according to the present law, it should be allowed. At the moment, there are ongoing discussions for a SynBio law which is not established, yet. For details, please have a look at our [[Team:LMU-Munich/Project_Safety | interview]].
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We did an interview with the Safety Commissioner Dr. Schubar who is responsible for the LMU-Munich. He confirmed that we are working with a safe strain (''B. subtilis'' W168 which has a tryptophan auxotrophy) and are only using safe plasmids, genes and promoters. He is not in a position to allow the release of our spores, but according to the present law, it should be allowed. At the moment, there are ongoing discussions for a SynBio law which is not yet established. For details, please have a look at our [[Team:LMU-Munich/Project_Safety | interview]].
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Our project offers a new safe platform for various applications. Similar to virus ghosts our spores are non-proliferative capsules and therefore are safer to work with than vegetative cells.  
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Our project offers a new, safe platform for various applications. Similar to virus ghosts, our spores are non-proliferative capsules and therefore are safer to work with than vegetative cells.  
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Part of the <b>Germination</b>STOP is the <b>Suicide</b>switch (see [[Team:LMU-Munich/Germination_Stop| '''Germination'''STOP]]) which yields a toxin during Sporulation and therefore kills the cell upon germination. This is a device dedicated to make our <b>Sporo</b>beads safe. But if linked to another Promotor it could be turned on in other cases and could therefore also make other systems safer.
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Part of the <b>Germination</b>STOP is the <b>Suicide</b>switch (see [[Team:LMU-Munich/Germination_Stop| '''Germination'''STOP]]) which yields a toxin during sporulation and therefore kills the cell upon germination. This is a device dedicated to make our <b>Sporo</b>beads safe. But if linked to another promotor, the switch could be turned on in other cases and be used to make other systems safer.
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Revision as of 13:03, 11 September 2012

iGEM Ludwig-Maximilians-Universität München Beadzillus

Team-LMU agar plates.resized.jpg

The LMU-Munich team is exuberantly happy about the great success at the World Championship Jamboree in Boston. Our project Beadzillus finished 4th and won the prize for the "Best Wiki" (with Slovenia) and "Best New Application Project".

IGEM HQ LMU prize.jpg

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