Team:LMU-Munich/Notebook/Safety

From 2014.igem.org

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To eradicate those concerns with BaKillus we developed a [https://2014.igem.org/Team:LMU-Munich/Project/BioBrickBox#Resistanc_free_strain_generation resistance free insertion strategy for Bacillus]. The W168 strain is auxotrophic for tryptophane as well, which is very limiting in the environment. Therefore BaKillus wont be able to compete with natural strains of ''B. subtilis''.
To eradicate those concerns with BaKillus we developed a [https://2014.igem.org/Team:LMU-Munich/Project/BioBrickBox#Resistanc_free_strain_generation resistance free insertion strategy for Bacillus]. The W168 strain is auxotrophic for tryptophane as well, which is very limiting in the environment. Therefore BaKillus wont be able to compete with natural strains of ''B. subtilis''.
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Additionally we aim at producing a combination of at least two antibiotics targeting different biochemical pathways within the same organism. It already has been proven, that treatment with combined antibiotics is effective against [http://cid.oxfordjournals.org/content/49/7/1072.full MRSA]
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Additionally we aim at producing a combination of at least two antibiotics targeting different biochemical pathways within the same organism. It already has been proven, that treatment with combined antibiotics is effective against [http://cid.oxfordjournals.org/content/49/7/1072.full MRSA].
To make sure BaKillus will not stay after it has fullfilled his duty, we worked on implementing a [https://2014.igem.org/Team:LMU-Munich/Project/Bakillus#suicide suicide switch].
To make sure BaKillus will not stay after it has fullfilled his duty, we worked on implementing a [https://2014.igem.org/Team:LMU-Munich/Project/Bakillus#suicide suicide switch].

Latest revision as of 20:45, 4 December 2014

Safety

Lab Safety

The LMU iGEM team has been instructed in all aspects of lab safety, according to German laws and the LMU work safety guidelines (see work), as well as safe handling of biological materials according to the same standards (see materials). Furthermore we received specific safety training corresponding to our workspace, including waste separation. All biological waste is autoclaved before disposal. Last but not least we were also instructed on the legal aspects of workplace accidents. Since we only work with BSL 1 organisms and DNA, all our work is done on open benches or under open-front hoods. For most procedures, basic protective gear (cotton lab coats & latex gloves) is sufficient. Some chemicals like ethidium bromide are only handled with nitrile gloves. Other experiments are conducted with safety glasses or UV face shields. Of course all team members wear clothes offering reasonable protection (flat, closed shoes etc.) in the lab.

LMU14 Keepcalm.png

GRAS Status

Our chassis of choice B. subtilis holds the GRAS-status, which is normally stated when talking about safe organisms. But what does GRAS actually mean?

GRAS is an acronym for "Generally Recognized As Safe". The term emerged 1958 from the Federal Food, Drug, and Cosmetic Act. The purpose of this Act was to ensure premarket review of food additives leading to approval by the FDA, the Food and Drug Administration. However, to avoid the FDA being paralized with recognition of basic food ingredients like flour and sugar, an exemption was made for substances that are commonly known to be innoxious. Consequently, the GRAS status was introduced.

The GRAS status inherits two components. First, technical evidence of safety, and second the condition that such evidence is both generally known and accepted. This must be confirmed by independent experts.

In 1997, the FDA also replaced the affirmation process through petitions with regulations that allow for mere notifications.

The GRAS list of the FDA doesn't claim to be complete. Substances can be GRAS without being recorded in the list already. But despite the GRAS classification, one should keep in mind that it doesn't guarantee ingredients are safe to be added to food indiscriminately. GRAS status can in fact contain restrictions and limitations.

References:

Safety Parts

One of Staphylococcus aureus' main characteristics is the ability to form biofilms on human epithelials. The combination of adhesion and the biofilm dissolving dispersin is meant to target S. aureus on the population level as well as on the cellular level to dispatch every individual S. aureus cell to avoid formation of new resistant strains.

When it comes to genetically modified organisms and their release into the environment, major concerns are raised concerning resistant phenotypes, that might be able to outcompete the natural strains in their original biological niche. To eradicate those concerns with BaKillus we developed a resistance free insertion strategy for Bacillus. The W168 strain is auxotrophic for tryptophane as well, which is very limiting in the environment. Therefore BaKillus wont be able to compete with natural strains of B. subtilis.

Additionally we aim at producing a combination of at least two antibiotics targeting different biochemical pathways within the same organism. It already has been proven, that treatment with combined antibiotics is effective against MRSA.

To make sure BaKillus will not stay after it has fullfilled his duty, we worked on implementing a suicide switch.


Hi there!

Welcome to our Wiki! I'm BaKillus, the pathogen-hunting microbe, and I'll guide you on this tour through our project. If you want to learn more about a specific step, you can simply close the tour and come back to it anytime you like. So let's start!

What's the problem?

First of all, what am I doing here? The problem is, pathogenic bacteria all around the world are becoming more and more resistant against antimicrobial drugs. One major reason for the trend is the inappropriate use of drugs. With my BaKillus super powers, I want to reduce this misuse and thus do my part to save global health.

Sensing of pathogens

To combat the pathogenic bacteria, I simply eavesdrop on their communication. Bacteria talk with each other via quorum sensing systems, which I use to detect them and trigger my responses.

Adhesion

The more specific and effective I can use my powers, the lower the danger is of provoking new resistance development. So I catch pathogens whenever I get hold of them and stick to them until my work is done.

Killing

Talking about my work - killing pathogens is finally what I am made for. In response to quorum sensing molecules of the pathogens, I export a range of antimicrobial substances leading to dissipation of biofilms and the killing of the targeted bacteria.

Suicide switch

When the job is done and all the bad guys are finished, you don't need a super hero anymore. So after fulfilling my work I say goodbye to the world by activating my suicide switch.

Application

Of course I'm not only a fictional hero, but a very real one. In two different prototypes, I could be used for diagnosis or treatment of pathogen-caused diseases. However, there is still a whole lot of regulational and economical questions that have to be answered before.

See you!

So now you know my short story - and it is time for me to return to my fight for a safer world. Feel free to take a closer look on my super powers, the process of my development or the plans for a medical application.