Team:Calgary/Project/Achievements

From 2014.igem.org

(Difference between revisions)
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<ul>
<ul>
-
<li>Designed and manufactured a prototype of informed design based on our biological system</li>
+
<li>Designed and manufactured a <span class="Blue">prototype</span> of informed design based on our biological system</li>
-
<li>Cost analysis of our prototype and system to ensure that this project is feasible in developing nations</li>
+
<li><span class="Blue">Cost analysis</span> of our prototype and system to ensure that this project is feasible in developing nations</li>
-
<li>Quantified the visible threshold of detection for several reporters using time-lapsed cell count and absorbance readings, as well as a programmed colour sensor</li>
+
<li><span class="Blue">Quantified</span> the visible threshold of detection for several reporters using time-lapsed cell count and absorbance readings, as well as a programmed colour sensor</li>
-
<li>Programmed an Arduino UNO microcontroller, colour sensor, and LCD screen to detect colour change among detection chambers, allowing for quantification of the colour</li>
+
<li><span class="Blue">Programmed</span> an Arduino UNO microcontroller, colour sensor, and LCD screen to detect colour change among detection chambers, allowing for quantification of the colour</li>
-
<li>Applied circuitry of a heating pad/temperature considerations for ideal isothermal PCR conditions</li>
+
<li>Applied circuitry of a heating pad/temperature considerations for <span class="Blue">ideal</span> isothermal PCR conditions</li>
-
<li>Used Autodesk Maya Software to visually model and represent our system</li>
+
<li>Used Autodesk Maya Software to <span class="Blue">visually model</span> and represent our system</li>
-
<li>Used Solid-works Software to model fluid flow analysis for different prototype designs</li>
+
<li>Used Solid-works Software to <span class="Blue">model</span> fluid flow analysis for different prototype designs</li>
</ul>
</ul>
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<ul>
<ul>
-
<li>Transformed <i>B. subtilis</i> with a primer product containing 125 bp of  
+
<li><span class="Orange">Transformed</span> <i>B. subtilis</i> with a primer product containing 125 bp of  
homologous sequence flanking our gene of interest</li>
homologous sequence flanking our gene of interest</li>
-
<li>Modified and optimized general transformation: characterized effect of  
+
<li>Modified and optimized general transformation: <span class="Orange">characterized</span> effect of  
-
changing xylose concentrations, temperature, and shaking?</li>
+
changing xylose concentrations, temperature, and shaking</li>
-
<li>Optimization of transformation in small, liquid volume</li>
+
<li><span class="Orange">Optimization</span> of transformation in small, liquid volume</li>
-
<li>Sporulated <i>B. subtilis</i></li>
+
<li><span class="Orange">Sporulated</span> <i>B. subtilis</i></li>
-
<li>Activated <i>B. subtilis</i> spores back to vegetative state</li>
+
<li><span class="Orange">Activated</span> <i>B. subtilis</i> spores back to vegetative state</li>
-
<li>Isolated the master regular for competency, <i>comK</i> from the genome of <i>B. subtilis</i>  
+
        <li>Isolated the master regular for competency, <span class="Orange"><i>comK</i></span> from the genome of <i>B. subtilis</i> using PCR and inserted it into a <span class="Orange">Biobrick</span> vector for future application as an iGEM standard part.  
-
using PCR and inserted it into a Biobrick vector for future application  
+
-
as an iGEM standard part.  
+
</ul>
</ul>
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<ul>
<ul>
-
<li>Demonstrated efficacy of isothermal PCR to amplify DNA sequences  
+
<li>Demonstrated efficacy of <span class="Blue">isothermal PCR</span> to amplify DNA sequences  
without the need of a thermocycler, using freeze-dried components</li>
without the need of a thermocycler, using freeze-dried components</li>
<li>Demonstrated ability to amplify target DNA sequence from whole  
<li>Demonstrated ability to amplify target DNA sequence from whole  
-
<i>E. coli</i> cells in a blood mixture</li>
+
<i>E. coli</i> cells in a <span class="Blue">blood mixture</span></li>
-
<li>Obtained specificity in target sequence primers - specific to numerous strains of  
+
<li>Obtained <span class="Blue">specificity</span> in target sequence primers - specific to numerous strains of  
<i>N. meningititis</i> but not other pathogens including a commensal strain of <i>N. meningititis</i>
<i>N. meningititis</i> but not other pathogens including a commensal strain of <i>N. meningititis</i>
Line 60: Line 58:
<ul>
<ul>
-
<li>Designed composite regulatory promoter sequences - used to allow repression of a downstream  
+
<li>Designed composite <span class="Orange">regulatory promoter sequences</span> - used to allow repression of a downstream reporter with a specific repressor. Includes 5 variants of repressible promoters in either single or  
-
reporter with a specific repressor. Includes 5 variants of repressible promoters in either single or  
+
triplicate repeats for variation in strength of repression</li>
triplicate repeats for variation in strength of repression</li>
-
<li>Demonstrated interaction (i.e. repression) between the reporter gene and repressor gene in  
+
<li>Demonstrated <span class="Orange">interaction</span> (i.e. repression) between the reporter gene and repressor gene in <i>E. coli</i></li>
-
<i>E. coli</i></li>
+
<li>Demonstrated the efficacy of <span class="Orange">homologous recombination</span> in <i>B. subtilis</i> and showed the minimum length of flanking sequences</li>
-
<li>Demonstrated the efficacy of homologous recombination in <i>B. subtilis</i> and showed the minimum  
+
<li><span class="Orange">Biobricked</span> and submitted the full-length <span class="Orange"><i>lacZ</i></span> gene, previously non-existent in the latest  
-
length of flanking sequences</li>
+
-
<li>Biobricked and submitted the full-length <i>lacZ</i> gene, previously non-existent in the latest  
+
distribution plates</li>
distribution plates</li>
-
 
+
<li>Constructed a <span class="Orange">reporter operon</span> consisting of a constitutive promoter (Pveg), ribosome binding site, operator (C1434) and reporter (LacZ/RFP).</li>
-
<li>Constructed a reporter operon consisting of a  
+
<li>Constructed a <span class="Orange">complementary repressor operon</span> consisting of a constitutive promoter (Pveg), ribosome binding site, and repressor pertaining to the operator. Repressor was also flanked with regions homologous to certain sequences within our pathogens of interest.</li>
-
constitutive promoter (Pveg), ribosome binding site, operator (C1434) and reporter (LacZ/RFP).</li>
+
-
<li>Constructed a complementary repressor operon  
+
-
consisting of a constitutive promoter (Pveg), ribosome  
+
-
binding site, and repressor pertaining to the operator.  
+
-
Repressor was also flanked with regions homologous to certain  
+
-
sequences within our pathogens of interest.</li>
+
</ul>
</ul>

Revision as of 01:57, 18 October 2014

Achievements

Policies and Practices:

  • Thoroughly researched our target markets and differing legislations that could affect our system
  • Connected with many different experts in the fields of infectious diseases, anti-malarial medications and public health to truly understand the needs and feasibility of the project
  • Connected with the foremost authority in low cost diagnostics, Foundation for Innovative New Diagnostics (FIND), to discuss the viability of our design and concept
  • Connected with a small village clinic in rural Uganda, which gave an opportunity to see the facility as well as discuss the topic with local physicians
  • Featured iGEM and our project on a global stage at the United Nations, in Geneva, and created discussion regarding the advancement of synthetic biology

Modelling:

  • Designed and manufactured a prototype of informed design based on our biological system
  • Cost analysis of our prototype and system to ensure that this project is feasible in developing nations
  • Quantified the visible threshold of detection for several reporters using time-lapsed cell count and absorbance readings, as well as a programmed colour sensor
  • Programmed an Arduino UNO microcontroller, colour sensor, and LCD screen to detect colour change among detection chambers, allowing for quantification of the colour
  • Applied circuitry of a heating pad/temperature considerations for ideal isothermal PCR conditions
  • Used Autodesk Maya Software to visually model and represent our system
  • Used Solid-works Software to model fluid flow analysis for different prototype designs

Transformation:

  • Transformed B. subtilis with a primer product containing 125 bp of homologous sequence flanking our gene of interest
  • Modified and optimized general transformation: characterized effect of changing xylose concentrations, temperature, and shaking
  • Optimization of transformation in small, liquid volume
  • Sporulated B. subtilis
  • Activated B. subtilis spores back to vegetative state
  • Isolated the master regular for competency, comK from the genome of B. subtilis using PCR and inserted it into a Biobrick vector for future application as an iGEM standard part.

Sample Preparation:

  • Demonstrated efficacy of isothermal PCR to amplify DNA sequences without the need of a thermocycler, using freeze-dried components
  • Demonstrated ability to amplify target DNA sequence from whole E. coli cells in a blood mixture
  • Obtained specificity in target sequence primers - specific to numerous strains of N. meningititis but not other pathogens including a commensal strain of N. meningititis

Detection/Genetic circuit

  • Designed composite regulatory promoter sequences - used to allow repression of a downstream reporter with a specific repressor. Includes 5 variants of repressible promoters in either single or triplicate repeats for variation in strength of repression
  • Demonstrated interaction (i.e. repression) between the reporter gene and repressor gene in E. coli
  • Demonstrated the efficacy of homologous recombination in B. subtilis and showed the minimum length of flanking sequences
  • Biobricked and submitted the full-length lacZ gene, previously non-existent in the latest distribution plates
  • Constructed a reporter operon consisting of a constitutive promoter (Pveg), ribosome binding site, operator (C1434) and reporter (LacZ/RFP).
  • Constructed a complementary repressor operon consisting of a constitutive promoter (Pveg), ribosome binding site, and repressor pertaining to the operator. Repressor was also flanked with regions homologous to certain sequences within our pathogens of interest.