Difference between revisions of "Team:UofC Calgary/Judging"

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<ul class="c-content-list-1 c-theme">
 
<li class="c-font-uppercase c-font-white">Part Characterization <a href="http://parts.igem.org/Part:BBa_K2008005"> BBa_K2008005</a></li>
 
<li class="c-font-uppercase c-font-white">Part Characterization <a href="http://parts.igem.org/Part:BBa_K2008005"> BBa_K2008005</a></li>
<p class="c-font-white"> This part contains an active nonamer from the Bowman Birk Protease Inhibitor (BBI) with the addition of lysine, serine, cysteine, and isoleucine (KSCI) tag on the N-terminal end and a phenylalanine (F) tag on the C-terminal end to increase BBI solubility. A <i>B. subtilis</i> secretory signal peptide sequence is included to allow for secretion of the peptide directly into surrounding media. A transdermal tag (TD1, BBa_K1074000) is fused to the N-terminus of BBI to allow for diffusion of the peptide across the skin. This coding sequence is under the control of the constitutive <i>B. subtilis promoter</i> pVeg (BBa_K143012) and a strong <i>B. subtilis</i> RBS (BBa_K780001).</p>
+
<p class="c-font-white" style="font-size: 12px"> This part contains an active nonamer from the Bowman Birk Protease Inhibitor (BBI) with the addition of lysine, serine, cysteine, and isoleucine (KSCI) tag on the N-terminal end and a phenylalanine (F) tag on the C-terminal end to increase BBI solubility. A <i>B. subtilis</i> secretory signal peptide sequence is included to allow for secretion of the peptide directly into surrounding media. A transdermal tag <a href="http://parts.igem.org/Part:BBa_K1074000">(TD1, BBa_K1074000)</a> is fused to the N-terminus of BBI to allow for diffusion of the peptide across the skin. This coding sequence is under the control of the constitutive <i>B. subtilis promoter</i> pVeg <a href="http://parts.igem.org/Part:BBa_K143012">(BBa_K143012)</a> and a strong <i>B. subtilis</i> RBS <a href="http://parts.igem.org/Part:BBa_K780001">(BBa_K780001)</a>.</p>
<p class="c-font-white">We characterized this part by testing the effect of the BBI peptide in cell culturing experiments using both wildtype fibroblasts (1BR3) as well as colon cancer cells (HCT116). We further characterized the delivery capabilities of our TD1 tag by administering patch prototypes to mice, and then performing mass spectrometry on the mice blood a few days after patch administration to detect the presence of our peptide in the mice blood.</p>
+
<p class="c-font-white" style="font-size: 12px">We characterized this part by testing the effect of the BBI peptide in cell culturing experiments using both wildtype fibroblasts (1BR3) as well as colon cancer cells (HCT116). We further characterized the delivery capabilities of our TD1 tag by administering patch prototypes to mice, and then performing mass spectrometry on the mice blood a few days after patch administration to detect the presence of our peptide in the mice blood.</p>
 +
<br>
 
<li class="c-font-uppercase c-font-white">Collaboration</li>
 
<li class="c-font-uppercase c-font-white">Collaboration</li>
<p class="c-font-white"> We have collaborated with various iGEM teams as well as certain local organizations for the improvement of our project and for the promotion of iGEM. See all of our collaborations on our <a href="https://2016.igem.org/Team:UofC_Calgary/Collaborations"> Collaborations</a> page.</p>
+
<p class="c-font-white" style="font-size: 12px"> We have collaborated with various iGEM teams as well as certain local organizations for the improvement of our project and for the promotion of iGEM. See all of our collaborations on our <a href="https://2016.igem.org/Team:UofC_Calgary/Collaborations"> Collaborations</a> page.</p>
 +
<br>
 
<li class="c-font-uppercase c-font-white">Human Practices</li>
 
<li class="c-font-uppercase c-font-white">Human Practices</li>
<p class="c-font-white">Our project was continually informed by discussions with professionals in the field. See our human practices efforts on our <a href="https://2016.igem.org/Team:UofC_Calgary/Human_Practices">Human Practices</a> pages. </p>
+
<p class="c-font-white" style="font-size: 12px">Our project was continually informed by discussions with professionals in the field. See our human practices efforts on our <a href="https://2016.igem.org/Team:UofC_Calgary/Human_Practices">Human Practices</a> pages. </p>
 
</ul>
 
</ul>
 
</div>
 
</div>
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<ul class="c-content-list-1 c-theme">
 
<ul class="c-content-list-1 c-theme">
<li class="c-font-white">
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<li class="c-font-white">Integrated Human Practices</li>
Integrated Human Practices
+
<p class="c-font-white" style="font-size: 12px"> See how the feedback we got from professionals fed back into our project design on <a href="https://2016.igem.org/Team:UofC_Calgary/HP/Gold"> Human Practices Gold</a> page. </p>
</li>
+
<br>
<p class="c-font-white"> See how the feedback we got from professionals fed back into our project design on <a href="https://2016.igem.org/Team:UofC_Calgary/HP/Gold"> Human Practices Gold</a> page. </p>
+
<li class="c-font-white">Improving upon a previous part <a href="http://parts.igem.org/Part:BBa_K1444018"> BBa_K1444018</a></li>
<li class="c-font-white">
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<p class="c-font-white" style="font-size: 12px"><i>B. subtilis</i> is a gram-positive bacterial species widely used in molecular biology labs around the world. It is capable of natural transformation under conditions of nutrient deprivation (energy starvation), and unlike many gram-negative species <i>B. subtilis</i> does not appear to require a specific uptake sequence. However, transformation through starvation may not be the most ideal process to implement in the lab as the protocols are very time-consuming, very sensitive to precise timings, and can be unreliable. Fortunately, all of the DNA uptake genes are under the control of a single transcription factor, so we can bypass the need for energy starvation by using cells derived from a specific strain of <i>B. subtilis</i> (SCK6) with the pAX01-comK plasmid constructed by Zhang (2010). </p>
Improving upon a previous part <a href="http://parts.igem.org/Part:BBa_K1444018"> BBa_K1444018</a>
+
<p class="c-font-white" style="font-size: 12px">This part contains a xylose-inducible promoter (pxylA), a ribosome binding site, and the comK coding sequence. This part is meant to be inserted into the genome of <i>B. subtilis</i> using an appropriate integration vector (unfortunately likely requiring the traditional transformation procedure). Once complete, you have a strain that can be transformed quickly and easily.</p>
</li>
+
<p class="c-font-white"><i>B. subtilis</i> is a gram-positive bacterial species widely used in molecular biology labs around the world. It is capable of natural transformation under conditions of nutrient deprivation (energy starvation), and unlike many gram-negative species <i>B. subtilis</i> does not appear to require a specific uptake sequence. However, transformation through starvation may not be the most ideal process to implement in the lab as the protocols are very time-consuming, very sensitive to precise timings, and can be unreliable. Fortunately, all of the DNA uptake genes are under the control of a single transcription factor, so we can bypass the need for energy starvation by using cells derived from a specific strain of <i>B. subtilis</i> (SCK6) with the pAX01-comK plasmid constructed by Zhang (2010). </p>
+
<p class="c-font-white">This part contains a xylose-inducible promoter (pxylA), a ribosome binding site, and the comK coding sequence. This part is meant to be inserted into the genome of <i>B. subtilis</i> using an appropriate integration vector (unfortunately likely requiring the traditional transformation procedure). Once complete, you have a strain that can be transformed quickly and easily.</p>
+
 
</ul>
 
</ul>
 
</div>
 
</div>

Revision as of 00:56, 17 October 2016

iGEM Calgary 2016

Bronze Medal didn't load. Please Refresh Page.

Bronze Requirements

  • Register and Attend
  • We have registered for and will be attending the 2016 iGEM Jamboree in Boston!


  • DELIVERABLES

  • Attributions
  • You can find the contributions of each of our members as well as our numerous amazing mentors on our Attributions page


  • New Part BBa_K2008003
  • We designed and characterized a gene construct coding for the radioprotective peptide mBBI attached to a secretion tag, TD1 tag for secretion and transdermal delivery, as well as GFP for easy transformation recognition. Find it on our parts page here

Silver Medal didn't load. Please Refresh Page.

Silver Requirements

  • Part Characterization BBa_K2008005
  • This part contains an active nonamer from the Bowman Birk Protease Inhibitor (BBI) with the addition of lysine, serine, cysteine, and isoleucine (KSCI) tag on the N-terminal end and a phenylalanine (F) tag on the C-terminal end to increase BBI solubility. A B. subtilis secretory signal peptide sequence is included to allow for secretion of the peptide directly into surrounding media. A transdermal tag (TD1, BBa_K1074000) is fused to the N-terminus of BBI to allow for diffusion of the peptide across the skin. This coding sequence is under the control of the constitutive B. subtilis promoter pVeg (BBa_K143012) and a strong B. subtilis RBS (BBa_K780001).

    We characterized this part by testing the effect of the BBI peptide in cell culturing experiments using both wildtype fibroblasts (1BR3) as well as colon cancer cells (HCT116). We further characterized the delivery capabilities of our TD1 tag by administering patch prototypes to mice, and then performing mass spectrometry on the mice blood a few days after patch administration to detect the presence of our peptide in the mice blood.


  • Collaboration
  • We have collaborated with various iGEM teams as well as certain local organizations for the improvement of our project and for the promotion of iGEM. See all of our collaborations on our Collaborations page.


  • Human Practices
  • Our project was continually informed by discussions with professionals in the field. See our human practices efforts on our Human Practices pages.

Gold Medal didn't load. Please Refresh Page.

Gold Requirements

  • Integrated Human Practices
  • See how the feedback we got from professionals fed back into our project design on Human Practices Gold page.


  • Improving upon a previous part BBa_K1444018
  • B. subtilis is a gram-positive bacterial species widely used in molecular biology labs around the world. It is capable of natural transformation under conditions of nutrient deprivation (energy starvation), and unlike many gram-negative species B. subtilis does not appear to require a specific uptake sequence. However, transformation through starvation may not be the most ideal process to implement in the lab as the protocols are very time-consuming, very sensitive to precise timings, and can be unreliable. Fortunately, all of the DNA uptake genes are under the control of a single transcription factor, so we can bypass the need for energy starvation by using cells derived from a specific strain of B. subtilis (SCK6) with the pAX01-comK plasmid constructed by Zhang (2010).

    This part contains a xylose-inducible promoter (pxylA), a ribosome binding site, and the comK coding sequence. This part is meant to be inserted into the genome of B. subtilis using an appropriate integration vector (unfortunately likely requiring the traditional transformation procedure). Once complete, you have a strain that can be transformed quickly and easily.

iGEM

iGEM is an international competition promoting synthetic biology as a means to solve social, economic and humanitarian problems around the globe. The iGEM Jamboree is held in Boston annually. In 2016, over 300 teams are competing against each other.

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Fully Trained!

Our entire team received a full BioSafety education from the University of Calgary! This entailed going to classes to prepare for a final quiz that tested our ability to be safe in the lab. Several of our members also had radiation training and clearance to ensure that work done with radiation was safe!

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Find us

Located in Calgary, Alberta, Canada.

  • University of Calgary
  • igem.calgary@gmail.com
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