Team:NTNU-Trondheim/Safety

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<p> We of course follow general lab safety and wear lab coats, disposable gloves and safety glasses when required by the safety guidelines and rules. The materials used in this project are mostly standard kits, restriction enzymes and buffers that are bought and come pre-made from biotechnology companies, and does not require any other safety precautions than the general ones already described above. This also goes for the preparation of solutions like growth medium and gels for gel electrophoresis. When doing gel electrophoresis we use GelRed instead of ethidium bromide, as it is said not to penetrate cell membranes and thus should not be able to work as a mutagen. However, to be on the safe side, we always wear nitrile gloves when working with GelRed.
<p> We of course follow general lab safety and wear lab coats, disposable gloves and safety glasses when required by the safety guidelines and rules. The materials used in this project are mostly standard kits, restriction enzymes and buffers that are bought and come pre-made from biotechnology companies, and does not require any other safety precautions than the general ones already described above. This also goes for the preparation of solutions like growth medium and gels for gel electrophoresis. When doing gel electrophoresis we use GelRed instead of ethidium bromide, as it is said not to penetrate cell membranes and thus should not be able to work as a mutagen. However, to be on the safe side, we always wear nitrile gloves when working with GelRed.
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<p> Our project does not inflict with any of the regulations, guidelines and acts set by the university, institute and government. None of the bacteria and BioBricks used or made in this project raises any serious safety issues for the public health, environment and security. Our activity and use of biological material corresponds to class 1 in the Norwegian regulation for protection against exposure to biological agents and use of GMOs. Class 1 cover use that does not involve any significant risk for human's and animal's health and environment. This corresponds to WHO risk group 1 in the classification of infective microorganisms.</p>
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<p> Our aim in this project is to make bacteria that fluoresce when stressed. This is not a property that is considered harmful or is related to the organism’s pathogenicity, infectivity or toxicity, and the strains of E. coli used (DH5alpha and TOP10) are non-pathogenic to people of normal health. Neither do they carry an F factor (fertility factor) and are therefore unable to perform conjugation. The strains used are optimized for lab use only and should not be able to survive in a foreign environment. Plasmids carrying genes for antibiotic resistance are used for selection, and the bacteria carrying these plasmids could in theory be of health and environmental concern if not handled properly. As a golden rule, GMOs should not under any circumstances be brought outside the lab. To overcome any possible safety issue in relation to the points described above, all biological material and equipment that has been in contact with this biological material are contained in special waste containers within the lab and autoclaved before disposal.</p>
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<p>If any of our organisms where to be released to an environment outside the lab, either by design or accident, the biggest threat in theory would be the transferring of genetic material and conferment of antibiotic resistance to other microorganisms in natural habitats and microorganisms related to human, animal or plant diseases. Antibiotic resistance is of huge concern when it comes to the treatment of infectious diseases and the risk of this happening should always be taken seriously and appropriate safety steps should be made. The steps described in this text, together with the set guidelines and rules, are considered sufficient to prevent this.</p>

Revision as of 09:13, 14 August 2013

NTNU Trondheim



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Safety


The university has a health, safety and environment (HSE) group with set guidelines and rules to regulate the work environment and safety. General information about this can be found at http://www.ntnu.edu/hse. Details on the HSE regulations for lab work can be found at http://www.ntnu.edu/hse/labhandbook. These are all based on the national biosafety regulations and guidelines set by the Norwegian Biotechnology Advisory Board (http://www.bion.no/english/norwegian-regulation) and the acts set by the government.

Lab work

The institute for Biotechnology has set some local guidelines and rules that apply for the specific labs that we use in our lab work for this project. The labs used are approved for work with gene-modified organisms (GMOs). Prior to the commencement of work in any of these labs, every person is given the essential training. The training covers the statutory regulations and safety provisions, the use of equipment and protective equipment, fire extinguishing, first aid, use of the chemical substances index and safety data sheets, proper waste disposal and reporting. The wetlab part of the NTNU iGEM team has all attended this training and is following the set lab guidelines and rules in their work.

We of course follow general lab safety and wear lab coats, disposable gloves and safety glasses when required by the safety guidelines and rules. The materials used in this project are mostly standard kits, restriction enzymes and buffers that are bought and come pre-made from biotechnology companies, and does not require any other safety precautions than the general ones already described above. This also goes for the preparation of solutions like growth medium and gels for gel electrophoresis. When doing gel electrophoresis we use GelRed instead of ethidium bromide, as it is said not to penetrate cell membranes and thus should not be able to work as a mutagen. However, to be on the safe side, we always wear nitrile gloves when working with GelRed.

Our project does not inflict with any of the regulations, guidelines and acts set by the university, institute and government. None of the bacteria and BioBricks used or made in this project raises any serious safety issues for the public health, environment and security. Our activity and use of biological material corresponds to class 1 in the Norwegian regulation for protection against exposure to biological agents and use of GMOs. Class 1 cover use that does not involve any significant risk for human's and animal's health and environment. This corresponds to WHO risk group 1 in the classification of infective microorganisms.

Our aim in this project is to make bacteria that fluoresce when stressed. This is not a property that is considered harmful or is related to the organism’s pathogenicity, infectivity or toxicity, and the strains of E. coli used (DH5alpha and TOP10) are non-pathogenic to people of normal health. Neither do they carry an F factor (fertility factor) and are therefore unable to perform conjugation. The strains used are optimized for lab use only and should not be able to survive in a foreign environment. Plasmids carrying genes for antibiotic resistance are used for selection, and the bacteria carrying these plasmids could in theory be of health and environmental concern if not handled properly. As a golden rule, GMOs should not under any circumstances be brought outside the lab. To overcome any possible safety issue in relation to the points described above, all biological material and equipment that has been in contact with this biological material are contained in special waste containers within the lab and autoclaved before disposal.

If any of our organisms where to be released to an environment outside the lab, either by design or accident, the biggest threat in theory would be the transferring of genetic material and conferment of antibiotic resistance to other microorganisms in natural habitats and microorganisms related to human, animal or plant diseases. Antibiotic resistance is of huge concern when it comes to the treatment of infectious diseases and the risk of this happening should always be taken seriously and appropriate safety steps should be made. The steps described in this text, together with the set guidelines and rules, are considered sufficient to prevent this.



Use this page to answer the questions on the safety page.



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