Team:Groningen/Safety

From 2010.igem.org

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ML-1 means that our organism (''Bacillus subtilis'') is non pathogenic and that the GMO we create is non pathogenic as well. Lolkema: “You could eat ''Bacillus'' if you want, so it is a really harmless bacteria!” To know if your GMO will be pathogenic or not, it is very important to know what function the DNA that you put in your organism has. It is allowed to insert DNA from a pathogenic organism, as long as the sequence you insert does not encode for pathogenic compounds. If you do not know the sequence and function of the DNA you insert in your host, you automatically work at ML-2 level, which has slightly stricter regulations. The main difference is that the door of ML-2 labs has to be locked when nobody is present, that you have to be even more careful and neat and that you have to fill in a labbook at the entrance of the lab to state your activities of that day. In an ML-1 lab a personal labbook in which you keep track of your experiments is enough.
ML-1 means that our organism (''Bacillus subtilis'') is non pathogenic and that the GMO we create is non pathogenic as well. Lolkema: “You could eat ''Bacillus'' if you want, so it is a really harmless bacteria!” To know if your GMO will be pathogenic or not, it is very important to know what function the DNA that you put in your organism has. It is allowed to insert DNA from a pathogenic organism, as long as the sequence you insert does not encode for pathogenic compounds. If you do not know the sequence and function of the DNA you insert in your host, you automatically work at ML-2 level, which has slightly stricter regulations. The main difference is that the door of ML-2 labs has to be locked when nobody is present, that you have to be even more careful and neat and that you have to fill in a labbook at the entrance of the lab to state your activities of that day. In an ML-1 lab a personal labbook in which you keep track of your experiments is enough.
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Everybody in the iGEM team needs to know what is in the lab permit for the project. It is the responsibility of the supervisor that the students know this. Since our supervisor works a lot with ''Bacillus subtilis'', a permit for working with this organism is easy to obtain. Another permit has to be requested to work with the chaplin genes from ''Streptomyces coelicolor'' and for the vectors used to insert the genes into ''Bacillus subtilis''. Both organisms are on the xxx list, so they are both considered safe and ML-1. Lolkema: When working with GMOs, one has to keep track of his or her experiments in a notebook. There has to be a table of contents at the beginning and a list of the GMO created at the end. In between the experiments should be described. This is necessary because an inspector has to be able to see what happens in a lab in an easy way.
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Everybody in the iGEM team needs to know what is in the lab permit for the project. It is the responsibility of the supervisor that the students know this. Since our supervisor works a lot with ''Bacillus subtilis'', a permit for working with this organism is easy to obtain. Another permit has to be requested to work with the chaplin genes from ''Streptomyces coelicolor'' and for the vectors used to insert the genes into ''Bacillus subtilis''. Both organisms are on the xxx list, so they are both considered safe and ML-1. Lolkema: “When working with GMOs, one has to keep track of his or her experiments in a notebook. There has to be a table of contents at the beginning and a list of the GMO created at the end. In between the experiments should be described. This is necessary because an inspector has to be able to see what happens in a lab in an easy way.
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In our project, we want to use our bacterium Bacillus subtilis to coat the surface for us. So when we want to coat the hull of a ship for example, living GMO would be released outside the lab. We were thinking to build a kill switch into the bacteria (enige uitleg hierover) which would let the bacteria die after they formed a biofilm (the coating). Lolkema: “A kill switch would solve your problems, because it is not allowed to bring living GMOs outside the lab, but genes of dead organisms are not a problem.” But first we would need living cells to coat our ships… Lolkema: “When you would take your project into production, you would have to go through several permit steps. First you need a permit to grow cultures larger than 10 Liters. Then you would need to do some field experiments which also need a special permit.” Since legislation only deals with living GMOs , we think that it would be easiest to make an ML-1 lab were the hull of the ship could be coated and than take the ship out of the lab after the cells have formed the coating and died due to our killswitch. This way there will be no living GMOs released in the environment during the coating process.
+
In our project, we want to use our bacterium ''Bacillus subtilis'' to coat the surface for us. So when we want to coat the hull of a ship for example, living GMOs would be released outside the lab. We were thinking to build a kill switch [[(link naar kill switch pagina)]] into the bacteria which would let the bacteria die after they formed a biofilm (the coating). Lolkema: “A kill switch would solve your problems, because it is not allowed to bring living GMOs outside the lab, but genes of dead organisms are not a problem. When you would take your project into production, you would have to go through several permit steps. First you need a permit to grow cultures larger than 10 Liters. Then you would need to do some field experiments which also need a special permit.” Since legislation only deals with living GMOs, we think that it would be easiest to make an ML-1 lab were the hull of the ship could be coated and than take the ship out of the lab after the cells have formed the coating and died due to our killswitch. This way there will be no living GMOs released in the environment during the coating process.
'''Biobricks'''
'''Biobricks'''

Revision as of 09:45, 25 August 2010

Safety

Safety regulations in the Netherlands

Last years team of the University of Groningen had a nice overview of the safety regulations in the Netherlands concerning GMOs on their safety page: [1].

ML1-4, lijst link uitleg

Safety at the university

Within the University of Groningen the organization of biological safety, including all activities that are carried out with genetically modified organisms (GMOs), is the legal responsibility of the Board of the University of Groningen. The Faculty Boards have been mandated by the Board of the University to implement the rules as set out in the GMO Regulations within their own faculty. Biological safety is ensured on the central level by a biological safety organization consisting of the biological safety officers (BSO) as well as a staff member of the Health, Safety and Environment Service (HSE). The HSE coordinates notifications, maintains the register and, in cooperation with the BSO, advises the Faculty Boards and the University Board in the field of biological safety. The central organization is complemented on the local level by responsible officers. BSO officers are members of the staff office and can report directly both to the University board and their own faculty. [2]

For each project a responsible officer will be appointed by the University Board on the recommendation of the Faculty Board. This officer is responsible for various aspects, including day-to-day matters concerning the activities involving genetically modified organisms. We consulted the local safety officer(Juke Lolkema), responsible for our iGEM project and asked him what his thougts about our project were.

For every action taken with GMOs, permission is needed. So for every project permission has to be requested via official forms. The building itself also has to be suitable for GMO experiments. iGEM is a student project and therefore rules for practical courses apply and our supervisors are responsible for the safety issues. Our biology building only has ML-1 and 2 laboratories. Our iGEM project is classified as ML-1, which means that normal rules for working with microorganisms apply. This includes working neatly, washing hands after working with GMO and keeping GMO waste separately so it can be autoclaved.

ML-1 means that our organism (Bacillus subtilis) is non pathogenic and that the GMO we create is non pathogenic as well. Lolkema: “You could eat Bacillus if you want, so it is a really harmless bacteria!” To know if your GMO will be pathogenic or not, it is very important to know what function the DNA that you put in your organism has. It is allowed to insert DNA from a pathogenic organism, as long as the sequence you insert does not encode for pathogenic compounds. If you do not know the sequence and function of the DNA you insert in your host, you automatically work at ML-2 level, which has slightly stricter regulations. The main difference is that the door of ML-2 labs has to be locked when nobody is present, that you have to be even more careful and neat and that you have to fill in a labbook at the entrance of the lab to state your activities of that day. In an ML-1 lab a personal labbook in which you keep track of your experiments is enough.

Everybody in the iGEM team needs to know what is in the lab permit for the project. It is the responsibility of the supervisor that the students know this. Since our supervisor works a lot with Bacillus subtilis, a permit for working with this organism is easy to obtain. Another permit has to be requested to work with the chaplin genes from Streptomyces coelicolor and for the vectors used to insert the genes into Bacillus subtilis. Both organisms are on the xxx list, so they are both considered safe and ML-1. Lolkema: “When working with GMOs, one has to keep track of his or her experiments in a notebook. There has to be a table of contents at the beginning and a list of the GMO created at the end. In between the experiments should be described. This is necessary because an inspector has to be able to see what happens in a lab in an easy way.”

In our project, we want to use our bacterium Bacillus subtilis to coat the surface for us. So when we want to coat the hull of a ship for example, living GMOs would be released outside the lab. We were thinking to build a kill switch (link naar kill switch pagina) into the bacteria which would let the bacteria die after they formed a biofilm (the coating). Lolkema: “A kill switch would solve your problems, because it is not allowed to bring living GMOs outside the lab, but genes of dead organisms are not a problem. When you would take your project into production, you would have to go through several permit steps. First you need a permit to grow cultures larger than 10 Liters. Then you would need to do some field experiments which also need a special permit.” Since legislation only deals with living GMOs, we think that it would be easiest to make an ML-1 lab were the hull of the ship could be coated and than take the ship out of the lab after the cells have formed the coating and died due to our killswitch. This way there will be no living GMOs released in the environment during the coating process.

Biobricks