Contents 1 Attributions & Contributions 1.1 Dr. A. William Smith 1.2 Mr. Doug Bray 1.3 Dr. Mark Roussel 1.4 Mr. David Lain Huston and the Arnott labs 2 Collaboration - Calgary iGEM 2.1 Materials and Methods 2.2 Results 2.3 Conclusion

Attributions & Contributions

The University of Lethbridge iGEM team would like to acknowledge the following people for their attributions and expertise which added to the success of our project, it is greatly appreciated, and has helped us gain new knowledge and skills.

Dr. A. William Smith

from The Department of New Media at the University of Lethbridge – For his assistance, knowledge, leadership and hard work, in the Biospirits film project.

Mr. Doug Bray

from The Faculty of Arts and Science at the University of Lethbridge – For his training and guidance of team members in the use of transmission electron microscopy.

Dr. Mark Roussel

from The Department of Chemistry and Biochemistry at the University of Lethbridge – For his assistance with protein modeling.

Mr. David Lain Huston and the Arnott labs

from The Institute of Cellular, Molecular, and Systems biology in Glasgow – For sending the team genes from the Xylene degradation pathway.

We are proud to say that all wet lab work was accomplished by undergraduate members of our iGEM team.

Collaboration - Calgary iGEM

We were asked by the Calgary iGEM team to to test the viability of their chassis to survive in tailings pond water. If E. coli DH5α cells containing one of our constructs can grow normally in medium prepared with tailings water, we can be confident that the chassis can be applied to tailings pond water in general.

Materials and Methods

50 mL of LB medium was made with tailings water and filtered through MILLEX filter Unit GS MF-Millipore MCE Membrane 0.22 µm in order to sterilize it and appropriate antibiotics were added. The tailings LB was inoculated with E. coli DH5α cells containing BBa_K331009 to an OD₆₀₀ of 0.1. The flask was incubated at 37˚C with shaking for 7 hours, during which photometric readings were taken every 30. Photometric readings were taken using the Pharmacia Biotech Ultrospec 3000, as the OD₆₀₀ readings reached 1.0 the solutions was diluted with LB media to keep the OD₆₀₀ reading between 0.1 and 1.0. The same protocol was used to observe cell growth of E. coli DH5α cells containing BBa_K331009 in 50 mL of LB medium made with MilliQ H₂O.

Results

Figure 1. OD₆₀₀ of E. coli DH5α cells containing BBa_K331009 cultured in LB medium made with tailings water (red) and LB medium made with MilliQ H₂O (black).

Conclusion

As seen in Figure 1, E. coli DH5α cells were able to grow in LB medium made with tailings water, suggesting that the chassis will survive for use in tailings pond water.