Team:British Columbia/Accomplishments

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<html><h3><center>UBC iGEM 2011 GOLD MEDAL, BEST MODEL, ADVANCING TO FINALS!!!</h3>
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<font size="+3"><font color="green">Wet Laboratory Achievements</font></font>  
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<center><img src="https://static.igem.org/mediawiki/2011/2/29/Ubcigemjamteam1.jpg" width=400px>&nbsp;&nbsp;&nbsp;<img src="https://static.igem.org/mediawiki/2011/5/5f/Ubcigemjamteam4.jpg" width=400px>
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Check out our Regionals <a href="https://2011.igem.org/files/presentation/British_Columbia.pdf">Presentation</a> and <a href="https://2011.igem.org/files/presentation/British_Columbia.pdf">Poster</a>.</b>
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<b></b>
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#part1 {width:300px; float:left; background-color: white; margin-left: 15px; margin-top:10px;}
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<font size="2"><h3>In vitro assay production of monoterpene in bacteria</h3></font>
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<b></b><font size="1"><h3>Geranyl Pyrophosphate (GPP) Assay</h3></font>
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<div id="part1">
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<b>The UBC iGEM team had a VERY successful weekend at the iGEM Americas Regionals synthetic biology research competition held this past weekend in Indianapolis. The UBC team earned a gold medal status for their research project AND won a special award for Best Model. This is the best showing for UBC ever and the team will now advance to the World Championships held at MIT in Boston, Nov 4-6th. We would like to thank everyone who has helped us for the inspiration, advice, patience, and support that you've provided for our talented set of students. We couldn’t have done it without you.</b></div><div id="part2">
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Alpha-pinene and Beta-pinene synthases were purified using His SpinTrap Ni-affinity columns and were assayed in vitro with GPP. Using gas chromatography-mass spectrometry (GCMS), we confirmed the synthesis of alpha and beta pinene monoterpenes from our enzyme assays.
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<b>2011 UBC iGEM Achievements:</b>
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</br></br>
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<b></b><font size="1"><h3>GC-MS Chromatogram</h3></font>
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UBC iGEM team earns a gold medal award for their research project on combating the
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<center>[[File:UBCiGEM_GC_beta_pinene.jpg]]</center>
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pine beetle outbreak by producing terpenes in yeast.
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</br></br>
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UBC iGEM team selected as finalist to advance to iGEM synthetic biology World
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<b></b>
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Championships at MIT in Boston, Nov 4-6.
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<font size="2"><h3>Diterpene production in yeast</h3></font>
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</br></br>
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UBC iGEM team wins special award for Best Model for their modelling work creating
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Levoabietadiene synthase was expressed in yeast and an in vivo assay was done. The samples were analyzed with GCMS. The products, abietadiene, neoabietadiene, levopimaradiene were produced. This shows that terpenes can be produced in yeast.
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both a MATLAB simulation of metabolic pathways to guide their work at the bench, and
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a model of the potential impacts on the pine beetle epidemic with data from the
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Ministry of Forestry.
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<b></b><font size="1"><h3>GC-MS Chromatogram</h3></font>
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</br></br>
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<center>[[File:UBCiGEM_GC_abidiene.jpg]]</center>
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UBC was one of only 10 Canadian teams in the Americas division. 68 teams in total
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<b></b>
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competed the Americas Regional Jamboree. Only 25 teams advanced to finals.
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<font size="2"><h3>Mountain Pine Beetle & Yeast Co-culture</h3></font>
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</br></br></div><div id="news">
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<h3>UBC Faculty of Applied Science Headline News</h3></html>
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To prove the effectiveness of our theoretical release model of Saccharomyces cerevisiae into the wild, we investigated whether wild-type yeast will survive during the transporation process (via the mountain pine beetles) from plate of origin (plate with yeast products; simulating our trapbox) to the next media plate. Beetles were incubated with yeast and were challenged with diferent amount of times away from the next media plates (in empty plates for 0, 10, 24, and 36 hours of time; simulating the transfer period when beetles leave the trapbox and fly off to the next tree). Results were analyzed qualitatively for the presence of GFP after growth on selective media plates from each time challenge. Based on these results, we can conclude that pine beetles do can carry wild-type yeast and transfer them onto the next media plate. It appears that our yeast product can survive on the beetles for 36 hours away from media plate. However, it cannot be determined whether the amount of yeast products on the beetles declines with time.
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<html><center><iframe width="425" height="349" src="http://www.youtube.com/embed/-fXdy8plAR8?hl=en&fs=1" frameborder="0" allowfullscreen></iframe></center></html>
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<center>[[File:Yst-MPB.jpg]]</center>
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<b></b>
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<font size="2"><h3>Blue Stain Fungi & Yeast Co-culture</h3></font>
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To determine whether terpene producing S.cerevisiae can grow with and/or inhibit the growth of G. clavigera, we co-cultured blue stain fungi with diterpene producing yeast and wild-type yeast in the same media. However, results are inclusive and we are currently optomizing the protocol for co-culturing.
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<center>[[File:3cocultureubcigem2011.jpg]]</center>
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<br>
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<br>
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<font size="+3"><font color="green">Modeling Achievements</font></font>
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<hr style="color:#BDCBBD; height:3px;" />
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<b></b>
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<font size="2"><h3>Monoterpene Production Model</h3></font>
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We modeled a simplified and modified version of the mevalonate pathway that describes our engineered yeast cells. We created a series of differential equations to model each chemical reaction that were based on first-order Michaelis-Menten kinetics. Enzyme constants were estimated/found using literature values and the simulations were conducted using MATLAB.
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Our simulation showed that 17.10% more beta-pinene is produced and 17.00 % more alpha-pinene is produced when K6R-hmg2 and erg20-2 are used instead of HMG2 and ERG20 alone in a yeast cell. For manufacturing purposes, sensitivity analysis was performed and it was determined that the pathway could be improved to increase the production of monoterpenes by increasing the concentration of the enzymes K6R-HMG2 and IDI1 for DMA-PP. In particular, the tripling the [K6R-HMG2] increases the [GPP] by 8.7000 times. The tripling the [K6R-HMG2] and [IDI1] for the production of DMA-PP increases the [B-pinene] by 7.3166 times and 1.3052 times respectively.
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<center>[[File:Monoterpene Production vs Time in Pinene Synthase.jpg]]</center>
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<b></b>
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<font size="2"><h3>Beetle Epidemic Model</h3></font>
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We employed a cluster-based modeling to predict the spread of mountain pine beetle infestation from year 2011 up to 2020 based on cluster analysis. In addition, we identified strategic subpopulation centres for deployment of synthetic products.
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<div id="links">
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<font size="2"><h3>Synthase Model</h3></font>
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We constructed 3D structure models of alpha-pinene, beta-pinene, and limonene synthase to identify amino-acid residues that can be modified in the future to improve terpene productions.
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<center>[[File:UBCiGEM skeletal dock.jpg]]</center>
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<font size="+3"><font color="green">Human Practices Achievements</font></font>
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<b></b>
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<font size="2"><h3>High School Mentorship</h3></font>
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We collaborated with Science World and Future Leaders in Science to deliver a synthetic biology workshop for local high school students. During our workshop, we introduced the idea of synthetic biology and iGEM to the high school students and guided them through a <html><a href="http://openwetware.org/wiki/IGEM_Outreach:Plasmid_Activity">plasmid activity</a></html> aimed at solving a real world problem by creating a plasmid with appropriate parts. Our workshop outline can be found at the wiki for <html><a href="http://openwetware.org/wiki/IGEM_Outreach:Life_in_the_Lab">iGEM outreach</a></html>. We also created a guide for building a high school iGEM team, which can be found <html><a href="https://static.igem.org/mediawiki/2011/a/ad/TeamBritishColumbiasGuidetoStartaHigh-schooliGEMteam.pdf">downloaded</a></html> or found on <html><b><a href="http://openwetware.org/wiki/IGEM_Outreach:Life_in_the_Lab">the CommunityBricks page</a></b></html>.
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<html></br><center><img src="https://static.igem.org/mediawiki/2011/b/b9/Ubcigemscienceworldoutreach.jpg" width=800px>
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<font size="2"><h3>Synthetic Biology Gone Wild</h3></font>
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Our project has the prospect  of introducing synthetic organisms into the environment, which is a controversial idea. First of all, we initiated an open dialogue, "Synthetic Biology in the Open: Pipe dream or the next giant leap for mankind?" which can be <html><a href="https://static.igem.org/mediawiki/2011/4/45/Ubcigem2011syntheticbiologyintheopen.pdf">downloaded</a></html> or found on <html><a href="http://openwetware.org/wiki/IGEM_Outreach:Synthetic_Biology_in_the_Open">this CommunityBricks page</a>.'''
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Next we conducted interviews with experts in our community to understand what the current attitudes are towards releasing synthetic biology in the wild.
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[http://blogs.apsc.ubc.ca/apscnews/2011/10/12/ubc-igem-team-wins-gold-medal-and-special-award-for-best-model/ UBC iGEM team wins gold medal and special award for best model]
 
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<html><h3>UBC Faculty of Science: Science Connect News and Events for UBC Science Alumni</h3></html>
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<center><img src="https://static.igem.org/mediawiki/2011/f/fe/UBCiGEM_skeletal_dock.jpg" width="50%" height="50%"</center>
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<b></b></center>
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<font size="2"><h3>Public Perceptions of Synthetic Biology</h3></font></html>
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From UBC orientation day, we collected students' perceptions on synthetic biology (presented in a word cloud)and observed whether it has changed for the past years.
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[http://science.ubc.ca/sites/science.ubc.ca/files/connect/2011_5/5-2011.htm UBC iGEM Team Has Winning Weekend]
 
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<html><h3>We have presented at the following events:</h3></html>
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<html><h4>What is Synthetic Biology?</h4>
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#'''aGEM, 24-25th September 2011:''' An annual competition held by Alberta Innovates Technology Futures in Edmonton where teams from Alberta (and British Columbia) showcase their iGEM projects.  
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<iframe id="xtranormal_What is Synthetic Biology?" name="xtranormal_What is Synthetic Biology?" style="width:480px;height:299px;" src="http://www.xtranormal.com/xtraplayr/12434771/what-is-synthetic-biology" marginwidth="0" marginheight="0" border="0" frameborder="0" scrolling="auto"></iframe>
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#'''iGEM Americas Regional Jamboree, 8-10th October 2011:''' Over 70 teams from all across the Americas competed at the Americas Jamboree for a chance at a spot at the World Championships. Our team won a Gold Medal and the Best Model special award!
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<img src="https://static.igem.org/mediawiki/2011/3/39/Ubcigemwordcloud2010.jpg" width="25%" height="25%" align="right" hspace="100">
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#'''UBC Microbiology and Immunology Symposium, 28th October 2011:''' The UBC iGEM team presented our project to the UBC Microbiology and Immunology department's faculty and students. This was a great opportunity to promote our presence at UBC, recruit new members, and also rehearse for the World Jamboree!
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#'''iGEM World Championship Jamboree, 5-7th November 2011:''' Finalist teams from all over the world will compete for best project, best track and other special awards!
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#'''Michael Smith Laboratories and CHiBi Colloquia, 8th November 2011:''' Immediately after our return from the World Jamboree, the UBC iGEM team will present our project to the faculty and students at the Michael Smith Laboratories! We have invited UBC's definitive news source, the Ubyssey to attend this presentation and feature our project in their student newspaper.
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<h3>Judging Requirements for Americas Regional Jamboree</h3>
 
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<font color=#A60901><b>Bronze:</b></font>
 
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# <b>Team registration</b>: <html><img src="https://static.igem.org/mediawiki/2011/a/ad/IGEM2011checkmark.PNG" width=25px height=20px></html>
 
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# <b>Complete Judging form</b>: <html><img src="https://static.igem.org/mediawiki/2011/a/ad/IGEM2011checkmark.PNG" width=25px height=20px></html> See [https://igem.org/2011_Judging_Form?id=517 Judging form] here.
 
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# <b>Team Wiki</b>:<html><img src="https://static.igem.org/mediawiki/2011/a/ad/IGEM2011checkmark.PNG" width=25px height=20px></html>
 
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# <b>Present a poster and a talk at the iGEM Jamboree</b>:<html><img src="https://static.igem.org/mediawiki/2011/a/ad/IGEM2011checkmark.PNG" width=25px height=20px></html>
 
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# <b>At least one new submitted and well-characterized standard BioBrick Part or Device</b>: We have submitted and characterized 4 new biobrick parts.
 
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<font color=#A60901><b>Silver:</b></font>
 
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# <b>Demonstrate that at least one new BioBrick Part or Device of your own design and construction works as expected</b> (See our <html><a href="https://2011.igem.org/Team:British_Columbia/Data">Data Page</a></html> for more details): We have demonstrated that the 4 parts we submitted are functional.
 
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# <b>Enter this information in the “Main Page” section of that Part’s/Device’s Registry entry</b>: The data pertaining to our biobrick parts have been added to the Registry.
 
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<font color=#A60901><b>Gold:</b></font>
 
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# <b>Improve the function of an existing BioBrick Part or Device and enter this information in the Registry</b> (See our <html><a href="https://2011.igem.org/Team:British_Columbia/Data">Data Page</a></html> for more details):
 
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## We sequenced the Registry’s IDI. Based on sequence discrepancies, we recommend that this part be removed from distribution.
 
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## We characterized GAL1 promoter and found it to be non-functional. We submitted our own functionally characterized GAL promoter.
 
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## We functionally characterized Limonene Generator in the Registry.
 
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# <b>Outline and detail a new approach to an issue of Human Practice in synthetic biology</b> (See our <html><a href="https://2011.igem.org/Team:British_Columbia/HP">Human Practices</a></html> for more details):
 
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## Guide for How to Start a iGEM High School team
 
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## Synthetic Biology in the Open
 
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## iGEM dictionary
 
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<h3>Project Accomplishments</h3>
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</html>

Latest revision as of 03:59, 29 October 2011

Team: British Columbia - 2011.igem.org

Wet Laboratory Achievements


Contents

In vitro assay production of monoterpene in bacteria

Geranyl Pyrophosphate (GPP) Assay

Alpha-pinene and Beta-pinene synthases were purified using His SpinTrap Ni-affinity columns and were assayed in vitro with GPP. Using gas chromatography-mass spectrometry (GCMS), we confirmed the synthesis of alpha and beta pinene monoterpenes from our enzyme assays.

GC-MS Chromatogram

UBCiGEM GC beta pinene.jpg


Diterpene production in yeast

Levoabietadiene synthase was expressed in yeast and an in vivo assay was done. The samples were analyzed with GCMS. The products, abietadiene, neoabietadiene, levopimaradiene were produced. This shows that terpenes can be produced in yeast.


GC-MS Chromatogram

UBCiGEM GC abidiene.jpg

Mountain Pine Beetle & Yeast Co-culture

To prove the effectiveness of our theoretical release model of Saccharomyces cerevisiae into the wild, we investigated whether wild-type yeast will survive during the transporation process (via the mountain pine beetles) from plate of origin (plate with yeast products; simulating our trapbox) to the next media plate. Beetles were incubated with yeast and were challenged with diferent amount of times away from the next media plates (in empty plates for 0, 10, 24, and 36 hours of time; simulating the transfer period when beetles leave the trapbox and fly off to the next tree). Results were analyzed qualitatively for the presence of GFP after growth on selective media plates from each time challenge. Based on these results, we can conclude that pine beetles do can carry wild-type yeast and transfer them onto the next media plate. It appears that our yeast product can survive on the beetles for 36 hours away from media plate. However, it cannot be determined whether the amount of yeast products on the beetles declines with time.


Yst-MPB.jpg

Blue Stain Fungi & Yeast Co-culture

To determine whether terpene producing S.cerevisiae can grow with and/or inhibit the growth of G. clavigera, we co-cultured blue stain fungi with diterpene producing yeast and wild-type yeast in the same media. However, results are inclusive and we are currently optomizing the protocol for co-culturing.

3cocultureubcigem2011.jpg



Modeling Achievements


Monoterpene Production Model


We modeled a simplified and modified version of the mevalonate pathway that describes our engineered yeast cells. We created a series of differential equations to model each chemical reaction that were based on first-order Michaelis-Menten kinetics. Enzyme constants were estimated/found using literature values and the simulations were conducted using MATLAB.

Our simulation showed that 17.10% more beta-pinene is produced and 17.00 % more alpha-pinene is produced when K6R-hmg2 and erg20-2 are used instead of HMG2 and ERG20 alone in a yeast cell. For manufacturing purposes, sensitivity analysis was performed and it was determined that the pathway could be improved to increase the production of monoterpenes by increasing the concentration of the enzymes K6R-HMG2 and IDI1 for DMA-PP. In particular, the tripling the [K6R-HMG2] increases the [GPP] by 8.7000 times. The tripling the [K6R-HMG2] and [IDI1] for the production of DMA-PP increases the [B-pinene] by 7.3166 times and 1.3052 times respectively.

Monoterpene Production vs Time in Pinene Synthase.jpg

Beetle Epidemic Model

We employed a cluster-based modeling to predict the spread of mountain pine beetle infestation from year 2011 up to 2020 based on cluster analysis. In addition, we identified strategic subpopulation centres for deployment of synthetic products.