The safety page is where users can see the safety precautions we took in lab. This includes sterilization techniques, lab rules, and biosafety ratings.

Safety Questions

1. Description of the Chassis organism(s) we used for this project

We used three different strains of ''E. coli'' including BL21, XL-Blue, and BM2.5. These were all Risk Group 1. ''E. coli'' are a human pathogen which causes irritation if it makes contact with skin or eyes. If the bacteria is injected, it can also cause irritation to the respiratory tract and kidneys. Below is the link for the risk assessment of our bacteria:

http://www.absa.org/riskgroups/bacteriasearch.php?genus+&species+coli

2. Our highest Risk Group used was Group 1

3. List of all new coding regions used in this project:

	Part Number	Where did you get the physical DNA for this part?	What species does this part originally come from?	What is the Risk Group of the species?	What is the function of this part, in its parent species?
1	BBa_K1225000	IDT	E. coli	1	Promoter
2	BBa_K1225001	IDT	E. coli	1	Promoter
3	BBa_K1225002	IDT	E. coli	1	Promoter
4	BBa_K1225003	IDT	E. coli	1	Promoter
5	BBa_K1225004	IDT	E. coli	1	Promoter

4. Do the biological materials used in your lab work pose any of the following risks?
1. Risks to the safety and health of team members or others working in the lab?
1. None of the biological materials pose risk to members. We worked only with GFP as a gene of interest with regulatory parts that do not function in isolation. We are not adding any viral DNA, toxins, or carcinogens that would pose a threat to the researchers. GFP has been used repeatedly and is well documented without evidence of risk to the safety of those who work with it directly.
2. Risks to the safety and health of the general public, if released by design or by accident?
1. None of the regulatory parts would be functional in isolation. The bacteria expressing these genes do not show viability changes and are not viable outside of the lab environment. GFP has not been shown to cause a safety or health risk to the general public, and our regulatory DNA has not shown any indication that this would change.

Researcher safety

For the majority of the project that we worked on there was limited safety issues that came up while working in lab. The parts that we worked with were parts that had previously been submitted in the parts registry particularly when working on the Robustness and standardization projects. The parts that we selected were chosen based on their availability and usefulness. These parts were primarily promoters, RBS, and terminators which are naturally found in E. coli. The reporter of interest was green fluorescent protein which although is not native in E. coli; however, it has been used for years in E. coli. When utilizing the BCDs, there was no immediate threat to the students and researchers. These were parts that were only used to regulate the amount of red fluorescent protein that was being expressed. As far as safety for our team while carrying out lab procedures, everyone was properly trained by an expert before using any and all laboratory equipment. Extensive training was performed before any team members were allowed to work in lab (see training certification). This ensured that everyone was aware of safety procedures such as handling biosafety level 1 material, disposal of waste materials, and proper lab equipment. Because we work in a shared lab space, special caution was taken to label every reagent, chemical, and solution made in lab. Placement of such materials were specified and labeled as well. This was in the case that something was dropped, misplaced, or handled by a researcher not in our lab group; they would be able to react appropriately. A buddy system was also put into place so that no one worked in lab by themselves during or after lab hours. This ensured that if an accident were to occur, help would be at hand.

Public safety

Because the projects that this year’s team took on do not have a direct link to the public, it was difficult to analyze the safety impact on the public. We focused on creating means to make engineering biology more of a reality; however, because synthetic biology is still at a young stage in this field’s history, the direct impact of what we have worked on cannot yet be estimated. The human practices aspect of our project delves into the deeper impact that we hope this project will have. However, as far as a direct impact in the near future, there is not a foreseeable public safety issue.

Environmental Safety

The biggest issues that came up over the course of this project that directly impacted the environment was the disposal of lab materials and chemicals. This was done through autoclaving waste and disposal through REM specifications. As far as the project outcomes affecting the environment, just as with the public safety issue there are no short term foreseeable safety issues that need to be addressed. Any issue that would arise would be an indirect use of our project to advance the field of synthetic biology. This was also covered in our human practices portion of our project.