"
Team:UC Chile2/Biosafety
From 2012.igem.org
m |
|||
| Line 6: | Line 6: | ||
<li><strong>Would any of your project ideas raise safety issues in terms of: | <li><strong>Would any of your project ideas raise safety issues in terms of: | ||
| - | </strong> | + | </strong></li> |
<ul> | <ul> | ||
<li><strong> researcher or public safety, </strong> </li> | <li><strong> researcher or public safety, </strong> </li> | ||
| Line 18: | Line 18: | ||
</li> | </li> | ||
<li><strong> Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues? | <li><strong> Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues? | ||
| - | </strong> | + | </strong></li> |
Yes, the release of biobricks made from Synechocystis genome´s sequences or at least with a region homologous to it raise the possibility of recombination by environmental cyanobacteria. To address this issue we have proposed and designed a biosafety mechanism discussed in question number 4 (see below). | Yes, the release of biobricks made from Synechocystis genome´s sequences or at least with a region homologous to it raise the possibility of recombination by environmental cyanobacteria. To address this issue we have proposed and designed a biosafety mechanism discussed in question number 4 (see below). | ||
Revision as of 20:18, 21 September 2012
Biosafety Questions
- Would any of your project ideas raise safety issues in terms of:
- researcher or public safety,
- environmental safety?
- Do any of the new BioBrick parts (or devices) that you made this year raise any safety issues?
- did you document these issues in the Registry?
- how did you manage to handle the safety issue?
- How could other teams learn from your experience?
- Is there a local biosafety group, committee, or review board at your institution?
- Do you have any other ideas how to deal with safety issues that could be useful for future iGEM competitions? How could parts, devices and systems be made even safer through biosafety engineering?
No pathogenic microorganisms or dangerous genes are considered in our ideas, in consequence our intended projects, if executed, do not represent any risk to researchers nor public safety.
As Synechocystis is a naturally competent environmental bacteria that undergoes homologous recombination, there is a posibility that if laboratory recombinant strains are leaked to the environment there may be environmental safety issues such as lateral DNA transference and endogenous species endangerment. We discuss this issue further in question number 4 (see below).
Yes, the release of biobricks made from Synechocystis genome´s sequences or at least with a region homologous to it raise the possibility of recombination by environmental cyanobacteria. To address this issue we have proposed and designed a biosafety mechanism discussed in question number 4 (see below).
Furthermore, our laboratory practices enforce strict methods to handle any biological material. As DNA is always hermetically contained or discarded with other biological material according to standard protocols we believe that our practices will not produce any environmental hazard.
All issues regarding our biobricks will be documented once we send the parts to the registry.
It has to be stated that any of the sequences designed and/or handled by our team are not per se dangerous nor they represent a fitness advantage to recombinant strains.
Our lab follows the Manual of Biosafety, established by the Superior Counsel of Science and Technological Development, from the National Fund of Scientific and Technological Development of Chile (FONDECYT).
Click here to download the Manual of Biosafety (Spanish)
To adress the possibility of recombinant Synechocystis cells being released from the lab, we've designed a recombination plasmid that knocks out the copS gene. This gene codes for a Cu-binding protein and is essential to Cu stress response in Synechocystis. It has been demonstrated that strains lacking this gene can´t survive in much lesser Cu concentrations found in drink water or natural water bodies (2).
We advice every team working in this chassis to adopt similar strategies. By designing integrative plasmids which interrupt fitness related genes, recombinant strains will be auxotrophic and/or hiper-susceptible. Thus, their recombinant cyanobacterial strains will be unable to thrive in natural environments.
Yes, there is a local biosafety panel in our institution. The Comitee of Bioethics and Biosafety of the Biological Sciences Faculty of the Pontifical Catholic University of Chile has reviewed our work and determined that the procedures involved in our project follow the bioethical and biosafety standards for research regulations provided by the Chilean Comission of Scientific and Technological Research (CONICYT).
Click here to download our Certificate from the Comitee of Bioethics and Biosafety
To prevent future problems and to encourage the construction of biosafe standard biological parts, we, UC_Chile team, propose the creation of the section “biosafety analysis” mandatory for all parts before their shipping to the registry. This way, it is assured that each new biobrick or device includes an assessment of the risks and biosafety advantages involved in its physical implementation.
Alongside the previous, we suggest the characterization of biosafety levels of other team’s constructs, making this practice analogous to the existing standard characterization of bricks. The requirement of this biosafety assessment for a team to win the gold medal would be a strong incentive.
Regarding to the molecular methods by which biosafety could be improved, we believe that the implementation of a lethal system to all iGEM plasmid backbones would prove essential. The system would kill the recombinant cells unless its action is inhibited by a compound present in the culture media but that its concentration in the environment is insignificant. That way, recombinant cells which are leaked to the environment will have no possibility to thrive in environmental conditions.
Concerning the last paragraph, we have already thought of such a system. We have found a perfect candidate gen to be placed under a constitutive promoter that produces cell lysis. Soon we will document more information about it in our wiki.
