Team:British Columbia/Notebook/22 July 2011

From 2011.igem.org

Team: British Columbia - 2011.igem.org

July 22 2011

Human Practices Laura is very excited to meet with Mrs. Anderson on Monday to discuss our teams involvement in the Future Science Leaders program at Science World! Science World British Columbia is a non-profit organization which engages British Columbians in science and inspires future science and technology leadership throughout our province. The Future Science Leaders is a program offered to high school students who are keen and bright and want to further their understanding of science. Through weekly meetings the program will cover several difference sciences such as biology, mathematics, technology, physical sciences, earth and space, and technology. We as an iGEM team have the privilege of presenting our project to this group of high school students and their parents. We will also be educating the students on the diverse applications of synthetic biology and give a brief tutorial about what synthetic biology is! There is also an opportunity to promote the idea of a high school iGEM team for next year. I am anticipating this meeting and hope to get some feedback and advice for other related Human Practice projects.

(-)-limonene

  • Re-do PCR to get the synthase off of the pET101 plasmid onto the yeast plasmid
    • Troubleshooting: Decrease the extension time to 30sec (15sec/1kb) with an annealing temperature of 70C
  • Transform original plasmid (pADM743) into DH5alpha cells

beta-pinene

  • cPCR colonies from biobrick plates (using G1004,G1005 primers)
    • Gel verification shows no bands
  • cPCR same colonies from biobrick plates using a new batch of G1004/G1005 primers as well as VF2/VR
  • Restriction Digest yeast plasmids and synthase
  • Ligate 8 versions together:
    • original + his-tagged + GAL
    • original + his-tagged + GDP
    • original + no-his + GAL
    • original + no-his + GDP
    • SDM + his-tagged + GAL
    • SDM + his-tagged + GDP
    • SDM + no-his + GAL
    • SDM + no-his + GDP
  • Transformation
    • Transformed ligated samples into E.coli