Team:BU Wellesley Software/Safety
From 2011.igem.org
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- | None of the materials used in our iGEM project pose a significant risk to the health and safety of our team members and laboratory. We work in a standard BSL1 certified lab space and mainly work with E. coli bacteria. Furthermore, there is no risk to the public health or environment if the materials of our project were released. This is because the genes that we are using and studying code for transcriptional proteins and are not pathogenic or toxic. There is no threat of security through misuse of our materials because of their nonlethal nature. | + | None of the materials used in our iGEM project pose a significant risk to the health and safety of our team members and laboratory. We work in a standard BSL1 certified lab space and mainly work with ''E. coli'' bacteria. Furthermore, there is no risk to the public health or environment if the materials of our project were released. This is because the genes that we are using and studying code for transcriptional proteins and are not pathogenic or toxic. There is no threat of security through misuse of our materials because of their nonlethal nature. |
- | Specifically, despite the design of our parts and devices focus on ''M.tuberculosis'' transcription factors, the actual genes we are implementing in our BioBrick devices are genes from the nonpathogenic strain of ''M.tuberculosis'', ''Mycobacterium smegmatis''. The genes are made from a PCR reaction using primers designed from the ''M. smegmatis'' genome. Additionally, we are inserting these genes into E. coli bacteria, thus we are never in contact or work directly with ''M. tuberculosis'' or ''M. smegmatis''. This eliminates any risks associated with our Biobrick devices affecting our team members as well as the overall public health and environment. The genes we are using are available to the public at http://www.tbdb.org/, thus there is no threat to security with our parts. | + | Specifically, despite the design of our parts and devices focus on ''M.tuberculosis'' transcription factors, the actual genes we are implementing in our BioBrick devices are genes from the nonpathogenic strain of ''M.tuberculosis'', ''Mycobacterium smegmatis''. The genes are made from a PCR reaction using primers designed from the ''M. smegmatis'' genome. Additionally, we are inserting these genes into ''E. coli'' bacteria, thus we are never in contact or work directly with ''M. tuberculosis'' or ''M. smegmatis''. This eliminates any risks associated with our Biobrick devices affecting our team members as well as the overall public health and environment. The genes we are using are available to the public at http://www.tbdb.org/, thus there is no threat to security with our parts. |
Revision as of 01:51, 22 August 2011
Safety
Safety is of the utmost importance to the wet lab division of the BU/Wellesley iGEM team. In our research exploration of transcription factor interactions in Mycobacterium tuberculosis, we strive to conduct experiments and construct DNA plasmids using the most biologically safe methods possible.
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