Our team embraces iGEM's spirit of innovation with a strong commitment to responsible research. We put safety and security at the center of our work - protecting people, our colleagues, and the environment - by designing, operating, and communicating responsibly.
As an iGEM team the biggest safety concern is the lab work, where it is crucial to have a clear understanding of the risk factors in play to ensure a successful and reproducible workflow. This is why we proactively map potential hazards in both our experiments and any future use, and we specify concrete countermeasures. To establish the needed safety measures, it is key to understand the specificities of the location and material we work with, as well as their limitations.
Hazard | Scenario | Mitigation |
---|---|---|
Environmental establishment of engineered algae | Culture escape or equipment failure | Kill switch + auxotrophy, closed systems, site-contained bioreactors only, emergency plans, inspections |
Ethidium bromide exposure | Gel prep/cleanup | Gloves, designated EtBr area, labeled waste, no skin contact |
Acrylamide (monomer) | Gel casting | Fume hood, gloves, full polymerization before disposal |
Methanol | Buffer prep/blotting | Fume hood, flammables cabinet, ignition control, spill kit |
Vessel or bioreactor leak | Breakage, human error | Secondary containment, sealed transport, SOPs, incident reporting |
Over-trusting AI predictions | Design choices based only on models | Treat as probabilistic, require experimental confirmation, documentation |
Field-like testing would only occur in the specialized, closed bioreactors at the wastewater plant to assess performance under real effluent conditions, since open release is prohibited. In Europe, such work requires prior authorization under EU Directive 2009/41/EC on contained use of GM microorganisms, along with approval from the national competent authority (e.g., Germany's BfR or France's HCB). Risk assessments, emergency plans, and regular inspections must be in place to demonstrate that the algae cannot escape into the wider environment.
*https://eur-lex.europa.eu/eli/dir/2009/41/oj
Being a team with people from multiple nationalities, we aim to investigate the possibility of a follow up on our project in a few different countries, more specifically France, Germany, and Switzerland. For both France and Germany this relies first hand on the fact that the activities are classified into risk classes 1-4 by EU Contained Use Directive 2009/41/EC. For European countries and Switzerland it also requires facility approval and activity notification/authorization before any further steps are taken. The typical is relatively similar, as the procedures have undergone a homogenisation on the European continent, but do have some key differences that we tried to underline in the following.
Who regulates? In Switzerland, contained use of GMOs is governed by the Containment Ordinance (SR 814.912). The Federal Office for the Environment (FOEN/BAFU) leads the process and operates the Ecogen portal/public register, with the Federal Office of Public Health (FOPH/BAG) covering human-health biosafety. Activities are filed as notifications for class 1-2 and authorizations for class 3-4 via the FOEN-coordinated process. Cantonal authorities may inspect and enforce the decisions taken.
Typical procedure
Sources: bafu.admin.ch, fedlex.admin
Who regulates? Applications for contained-use facilities and genetic engineering operations are processed by the competent authority of the federal state (Land) where the facility is located. For class 3-4 work, the federal ZKBS (Central Committee on Biological Safety) must be consulted for an opinion. ZKBS then provides risk assessments, containment level assignments, and organism guidance (including searchable microorganism database). For GM food/feed authorisation (not our case) the procedure is to go through the BfR (Bundesinstitut für Risikobewertung).
Typical procedure
Sources: bvl.bund.de, Bundesinstitut für Risikobewertung, zkbs-online.de
Who regulates? The ministry of research and higher education (MESR) is the competent authority for contained use in research/teaching. Contact points and portals are provided by MESR, with some deliberate release cases further scrutinised by the ministry of ecological transition.
Since 1 Jan 2022, France simplified some class 1 procedures and reorganized regulatory bodies. MESR now provides the operational guidance and handles filings.
Typical procedure
Sources: French Public Health guidance, legifrance.gouv.fr, enseignementsup-recherche.gouv.fr
This contained algal bioprocess aims to recover REEs safely from industrial/wastewater streams and may also reduce pollutant loads. The combination of genetic safeguards, physical containment, and institutional procedures keeps risks as low as reasonably achievable while enabling responsible innovation.
Safety considerations guide our engagements with partners and communities. When we discuss potential deployments, we emphasise how containment designs, wastewater expertise from EAWAG, and institutional oversight shape the project roadmap. We document feedback, communicate realistic risk narratives, and plan to include findings from our interviews (including the EAWAG session) as soon as they are cleared for publication.