IGEM:Paris Bettencourt 2012/Previous Biosafety iGEM Projects: Difference between revisions
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| <center> [http://2011.igem.org/Team:St_Andrews Kill switch engage!] </center> | | <center> [http://2011.igem.org/Team:St_Andrews Kill switch engage!] </center> | ||
| Kill switch | | Kill switch | ||
| | | <Kill switch.> Our kill switch is designed by inserting an antimicrobial peptide (AMP) gene into E.Coli [http://2011.igem.org/Team:St_Andrews/biosafe Read More] | ||
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Revision as of 13:24, 27 May 2012
Notebook | Design | Roadmap | Meetings and to-dos | Protocols | Bibliography | Previous Biosafety iGEM projects |
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Team | Year | Project Name | Project Summary | Biosafety Idea |
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Kill switch | <Kill switch.> Our kill switch is designed by inserting an antimicrobial peptide (AMP) gene into E.Coli Read More | |||
Engineer bacteria to accelerate plant root development | Toxin/antitoxin. Consits of the insertion of the Holin + Endolysine and Anti Holin genes. Read More | |||
Bacteria that detects and signals the presence of nitrates | Encapsulation in a gel. We encapsulated our bacteria in beeds made out of a non toxic gel.Read More | |||
Detect chitin,and alert the plant by stimulating an early hypersensitive response against infection. | A few ideas but no design:
1. amplification mostly from start to stop codon to avoid hidden pathogenicity + blast of sequences to confirm 2. Cloning in vectors without a mobilizable origin or TRA region. 3.growth curve of the strain to confirm low dissemination. 4. develop a strategy to monitory the presence of the modified bacteria in the crops fields based on color markers (no design made). Read More | |||
Heavy metal bioreporter and bioabsorbent engineering | A few superficial ideas
(1. make the plasmid toxic for any bacteria it may transfer to. 2. plasmid can’t be replicated in another bacteria) Read More | |||