Team
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Year
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Project Name
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Project Summary
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Biosafety Idea
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St. Andrews
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2011
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Kill switch engage!
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Kill switch
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Kill switch. Our kill switch is designed by inserting an antimicrobial peptide (AMP) gene into E.Coli
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Imperial College
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2011
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Auxin
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Engineer bacteria to accelerate plant root development
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Toxin/antitoxin. Consits of the insertion of the Holin + Endolysine and Anti Holin genes.
- Holin is a protein that forms pores in cell membranes
- Anti-holin binds to holin, inhibiting it's action.
- Once pores are formed by holin, lysozyme can access the periplasmic space and degrade the cell wall, causing cell lysis.
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Bristol
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2010
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AgrEcoi
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Bacteria that detects and signals the presence of nitrates
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Encapsulation in a gel. We encapsulated our bacteria in beeds made out of a non toxic gel.
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Colombia
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2011
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Defense aid for coffee plantations against fungi ("Detect and alert" system)
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Detect chitin,and alert the plant by stimulating an early hypersensitive response against infection.
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A few ideas but no design:
- Amplification mostly from start to stop codon to avoid hidden pathogenicity + blast of sequences to confirm
- Cloning in vectors without a mobilizable origin or TRA region.
- Growth curve of the strain to confirm low dissemination.
- Develop a strategy to monitory the presence of the modified bacteria in the crops fields based on color markers (no design made).
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British Columbia
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2011
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iSynthase
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Optimize production of terpenes in Saccharomyces cerevisiae yeast (to help trees fight invading beetles and fungi)
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A few ideas (no design):
- Contain a tracking system to detect their presence e.g. a non-coding DNA code akin to a fingerprint
- Contain a suicide system to enable effective elimination of the organism when so desired
What experts say
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Peking
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2010
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Heavy metal decontamination kit
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Heavy metal bioreporter and bioabsorbent engineering
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A few superficial ideas:
- Make the plasmid toxic for any bacteria it may transfer to.
- Plasmid can’t be replicated in another bacteria
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Brown-Stanford
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2011
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REGObricks
PowerCell
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Projects which could be useful for a space travelling:
- REGObricks brings the principle of In-Situ Resource Utilization to bear on the problem of constructing, maintaining and expanding shelter for human inhabitants on the desolate Martian landscape.
- By producing macromolecules essential to bacterial growth, PowerCell will form a metabolic foundation for the biological systems which will eventually enable a settlement on Mars.
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Not about biosafety, but:
- The team used GelRed, a DNA dye produced by Biotium Inc, as a non-toxic alternative to ethidium bromide (EtBr). Let's use it too!
They do not believe that their BioBrick parts will have any negative effect on the environment. But they could be interested by our project!
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KULeuven
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2011
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E.D. FROSTI
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CONTROLLING ICE FORMATION.
- Bacterium E.D. Frosti induces ice crystallization, using the ice-nucleating protein (INP), or inhibits ice crystal formation, using the anti-freeze protein (AFP), depending on the given stimulus.
- These proteins will be extracellularly anchored at E.D. Frosti’s cell membrane.
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Suicide mechanism: DNA nuclease.
- Destruction of the DNA > bacteria dies, but keeps its shape so it can still do its job (functional protein are at the surface of the membrane).
- The suicide mechanism activity is mediated by an “AND”-gate system: the cell death mechanism is only activated when one of the two stimuli is given, AND a sudden decrease in temperature (a cold-shock) occurs
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LMU-Munich
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2011
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Metal Sensor
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Biosensor to detect metals in waste water
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One idea (no design):
- Every potentially pathogenic or hazardous biobrick should be cloned in a special backbone containing the sequences of the present backbones AND an inducible killing gene cassette.
- This killing cassette is induced by a normaly absent reagent that could easily be added in case of contamination
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Lyon-INSA-ENS
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2011
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Cobalt Buster
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Decontamination of radioactive cobalt in water by a biofilm
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Biofilm & Adherence =
- confinement bacterias
- easy purification of water
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METU-Ankara
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2011
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MethanE.COLIc
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Sensing methane gas and converting it into methanol
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Kill switch = Toxin temperature induced
- Holin + Endolysine
- Induced when T°>42°C
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Caltech
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2011
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Bioremediation of Endocrine Disruptors Using Genetically Modified Escherichia Coli
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Endocrine-disrupting chemicals (EDCs) are chemicals that interact with the endocrine system by binding to hormone receptors, causing problems in sexual development and reproduction of organisms
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Biosafety ideas:
- Water filtration system for containment of microbes (filters all microbes, does not retain free DNA).
- Use the ccdB gene (BBa_P1016 and BBa_P1010)on a plasmid in conjunction with an E. coli strain such as DB3.1 (BBa_V1005). The plasmid will code for the “death gene” which will kill any cell that does not code for immunity in its genome. If a native microorganism would uptake this man-made plasmid, it would die, preventing the propagation of the recombinant DNA in the environment (Featured Parts: Cell Death).
- Another similar “suicide” containment system uses streptavidin (BBa_J36841) (Kaplan, Mello et al. 1999; Urgun-Demirtas, Stark et al. 2006). This protein binds very tightly to biotin, a required co-enzyme for many metabolic pathways. This makes biotin unavailable and causes cell death. Kaplan et al. reported cell counts were reduced 99.9% in eight hours after their system was activated by absence of pollutant to degrade.
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Berkeley
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2010
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Bioremediation of Endocrine Disruptors Using Genetically Modified Escherichia Coli
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Choa Choa's Delivery Service
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Clotho Framework:
Clotho implements the current biosafety standards as outlined by the NIH and the CDC. Whenever a new part is instantiated, Clotho BLAST's its sequence against a databank of known virulence factors and pathogens and returns the RG number of the highest match. This framework ensures that every part in Clotho has a RG value associated with it. In addition, when composite parts are made by joining basic parts, the composite part is also assigned a BSL number. Finally, all strains in Clotho have a risk group.
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WITS-CSIR_SA
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2011
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Biotweet
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Engineer bacteria to allow them to transport packets of chemicals, and then form a network.
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Promoter responsive to synthetic chemicals not present in nature.
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ULB-Brussels
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2011
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One-step gene insertion or deletion system
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An easy way to allowing the insertion and/or deletion of genes in the E. coli chromosome in a minimal number of steps
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FLP recombination to remove resistance gene, eg. FRT - Cm - FRT will remove the Cm resistance gene
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Johns Hopkins
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2011
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VitaYeast
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They want to make bread with yeast producing Vitamin
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their yeast strain lacks functional pathways for seven essential aa.
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Kyoto
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2009
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p1 : Gene Switch Depending on Duplication
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How to express a gene after a certain lifespan. The use Linear DNA, in which a repressor will be degraded after few cell division.
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"they want to control exact cell’s life time (or death time) depending on the number of cell division times.
They get rid of the exonucelase problem by inserting multiple protein binding site that will be degraded when division occurs, but not with exonucleases. The repressor gene is degraded after a certain time."
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UNICAMP-EMSE_Brazil
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2011
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stress wars
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Coli based production of anti-stress compounds in the organism to improve the quality of life
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"no design but two suggestions :
One suggestion in the biosafety of the researcher is to include in the iGEM parts kit the bacterial less endotoxicchassi (developed by Berkeley UC 2007), to avoid serious septic problems in the case of an accident that leads to an intense contact with the bacteria (eye or bloodstream contact, inhalation or ingestion).
Another suggestion for population and environment safety is to (somehow) include in all biobricks an operating unit that detects if the bacteria is not in a culture media (detects some molecule produced through the metabolism of a specific media constituent) and express lysozyme to kill it if it's released in the environment (idea inspired by Team UNICAMP-Brazil 2009)."
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Illinois-Tools
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2009
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Interactive Metabolic Pathway Tools (IMP Tools)
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Open source, web based program that involves model-guided cellular engineering where new metabolic functions can be added to existing microorganisms.
- It takes a user-defined input compound, output compound, and weighting scheme and determines the ideal pathway from the starting to the ending compound
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By limiting ATP produced we lessen the chances of a cell growing vigorously and being a potential danger to the environment.
- The actual means to prevent this is by creating a script that will analyze ATP consumption and production.
- With this information, you are able to adjust the ATP metabolism in whatever way you want.
- You will be able to keep the production low enough so cell processes can still occur and allow the cell to grow to an extent but not high enough that it can potentially grow out of control
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Harvard
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2009
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Optical communication
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Our team has constructed a system that allows for interspecies, bacteria-to-yeast optical communication
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A bacterial blackboard using a yeast two hybrid system and luciferase proteins. The blackboard can only be activated with a certain frequency of light, and must be erased with a different frequency of light.
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Michigan
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2009
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The Toluene Terminator
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The Toluene Terminator is a Pseudomonas putida device that aims to:
- identify the toxic compound toluene in an environmental setting (e.g. a spill into soil from an underground petrol tank),
- move to and uptake it,
- metabolize it,
- destroy itself when all of the toluene has been metabolized.
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A kill switch that operates through the Enterobacteria phage T4 Lysis Device (lysozyme, holin, and antiholin) created by the Berkley 2008 team. We proposed two mechanisms for cell lysis:
- arabinose inducible suicide mechanism
- suicide mechanism with tunable repression.
See the designs
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