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Team:British Columbia/Notebook/Week 11
From 2011.igem.org
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==Lab Meeting - August 15== | ==Lab Meeting - August 15== | ||
At the meeting today, we briefly talked about getting more sponsors. We also began discussing the design for the team t-shirts as well as potential activities for Imagine Day (This is a one day orientation mainly targeted towards first years; however, there is a main event in the afternoon where clubs such as ourselves can set up booths to inform the new and returning students of the resources and extracurricular activities that are available to them). | At the meeting today, we briefly talked about getting more sponsors. We also began discussing the design for the team t-shirts as well as potential activities for Imagine Day (This is a one day orientation mainly targeted towards first years; however, there is a main event in the afternoon where clubs such as ourselves can set up booths to inform the new and returning students of the resources and extracurricular activities that are available to them). | ||
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==1,8-cineole== | ==1,8-cineole== | ||
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The pg-cineole biobrick has been unsuccessful up to this point, but another round of PCR to attach the biobrick suffix and prefix was quite successful. Previously, Jacob was using the annealing temperature of just where the primer would bind to the original synthase, but it was pointed out that in a PCR reaction, all subsequent same-direction amplifications after the first one attach fully, raising the Tm. Using the new Tm, the PCR worked far better. The ligation and transformation were also successes. | The pg-cineole biobrick has been unsuccessful up to this point, but another round of PCR to attach the biobrick suffix and prefix was quite successful. Previously, Jacob was using the annealing temperature of just where the primer would bind to the original synthase, but it was pointed out that in a PCR reaction, all subsequent same-direction amplifications after the first one attach fully, raising the Tm. Using the new Tm, the PCR worked far better. The ligation and transformation were also successes. | ||
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| + | ==beta-Pinene== | ||
| + | Still working on getting the original synthase onto a yeast plasmid containing GPD promoter, she re-dos the ligations using a 6:1 ratio instead of 3:1. She then transforms the product into <i>E.coli</i>. | ||
| + | Vicki also digests and ligates the original synthase and the yeast plasmid (GAL) together and transforms that into <i>E.coli</i>. | ||
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==Characterization: Limonene Synthase (LIMS1) - Part BBa_I742110== | ==Characterization: Limonene Synthase (LIMS1) - Part BBa_I742110== | ||
Revision as of 22:21, 21 August 2011
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Lab Meeting - August 15
At the meeting today, we briefly talked about getting more sponsors. We also began discussing the design for the team t-shirts as well as potential activities for Imagine Day (This is a one day orientation mainly targeted towards first years; however, there is a main event in the afternoon where clubs such as ourselves can set up booths to inform the new and returning students of the resources and extracurricular activities that are available to them).
1,8-cineole
There are colonies on the yeast plates! They remained very small even on the fifth day after plating, but the fact that they were present means that Jacob can proceed with the gc-ms.
Only the synthases that had undergone SDM were used to transform the yeast so far. In order to check that there was no change in the expression due to the silent mutations that Jacob introduced with the SDM, he prepared shuttle vectors to get the original synthase into yeast.
The pgxe-cineole biobrick seems to be correct, so Jacob plans to make a glycerol stock of it, as well as submit the biobrick to the parts registry. Hurrah! We have a part!
The pg-cineole biobrick has been unsuccessful up to this point, but another round of PCR to attach the biobrick suffix and prefix was quite successful. Previously, Jacob was using the annealing temperature of just where the primer would bind to the original synthase, but it was pointed out that in a PCR reaction, all subsequent same-direction amplifications after the first one attach fully, raising the Tm. Using the new Tm, the PCR worked far better. The ligation and transformation were also successes.
beta-Pinene
Still working on getting the original synthase onto a yeast plasmid containing GPD promoter, she re-dos the ligations using a 6:1 ratio instead of 3:1. She then transforms the product into E.coli. Vicki also digests and ligates the original synthase and the yeast plasmid (GAL) together and transforms that into E.coli.
Characterization: Limonene Synthase (LIMS1) - Part BBa_I742110
Vicki digested and ligated following samples:
- limonene synthase + yeast plasmid with GPD promoter
- limonene synthase + yeast plasmid with GAL promoter
She then transformed the products into E.coli cells. Waiting for results...
Characterization: GPD-GFP
We looked at the expression of GFP as regulated by the yeast GPD promoter under a fluorescence microscope...
We will be submitting the GPD promoter as a new Biobrick part and also use it as a standard of comparison for the GAL promoter already in the Parts Registry.
Team Bonding
Today we got together and took our first whole team photos. Check out the one on our team page.
