"

From 2011.igem.org

Home

Team

Project

Modeling

Notebook

Safety

Attributions

Sponsors

You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing.
Our project this year is to design, create, and test a working cadmium water tester. We are going to do this by altering the existing biochemical pathway that Yeast has to recognize the cadmium, and then create our own code that will make it fluoresce red. When we originally had the idea for a water tester, we looked for metals, pesticides, and other harmful substances that are a problem in water supplies. Through much research, we found that cadmium is often a byproduct of many industrial processes, and is often leaked or exposed to the environment. Also, yeast recognizes the presence of cadmium already, so we figured it would be much more simple to alter an existing pathway than to create an entirely new one. We hope through research and experimentation that we are able to make cadmium much more detectable in the environment.
	Greenfield-Central High School Team Rihm

Apr 2011 Sun Mon Tue Wed Thu Fri Sat           1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30

May 2011 Sun Mon Tue Wed Thu Fri Sat 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31

Jun 2011 Sun Mon Tue Wed Thu Fri Sat       1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30

April 13th:

Officially met for the first time and discussed ideas for our project. Some of the original ideas included a strain of yeast that acted as a water tester, a strain of yeast that emitted a cinnamon scent, and a strain of yeast that reverses the oxidation of copper.

April 20th:

After we read an article on how yeast copes with toxic metals (Wysocki & Tamas, 2010), we made the final decision of making a water tester. We discussed what metals we wanted to detect in an environment, and we decided on copper, becase yeast already has a promoter associated with copper, Cup1.

April 23th:

We met early in the morning and discussed how to actually make our plasmid. We read about and decided to use Ura3 as our building block, and that we were going to put our plasmid in Ura3 (Mumberg, Muller, & Funk, 1995). We learned about the Gibson Method, a new system of putting together DNA parts instead of using restrictive enzymes. We also learned the order of our part: Promoter, Kozak Sequence, Space, Protein Coding Region, and then Terminator.

April 27th: We changed our project goal, and decided to use Cadmium after reading that cadmium pollution is a much bigger problem than copper pollution, and has a greater detrimental effect on the human body.

Citations:

Jeyaprakash, A., Welch J.W., Fogel, S. (1991) Multicopy CUP1 plasmids enhance cadmium and copper resistance levels in yeast. Molecular and General Genet. 363-368.

Mumberg, D., Muller, R., & Funk, M. (1995) Yeast vectors for the contolled expression of heterologous proteins in different genetic backgrounds. Elsevier Science B.V. 119-122.

Wysocki, R. & Tamas, M.J. (2010) How Saccharomyces cervisiae copes with toxic metals and metalloids. Federation of European Microbiology Societies Microbiology Review 925-951.