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Team:NYMU-Taipei

From 2013.igem.org

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Revision as of 02:29, 18 July 2013 (view source)
Blackrabbit (Talk | contribs)
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Latest revision as of 02:41, 29 October 2013 (view source)
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{{:Team:NYMU-Taipei/Frontpage}}
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==Overview of 2013 NYMU iGEM Team Project==
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To save bees from ''Nosema ceranae'' infection, the culprit of colony collapse disorder (CCD), NYMU-Taipei iGEM team has  created the so-called ''Bee. coli'' from ''Escherichia coli'' MG1655, which naturally resides in bees. The ''Bee. coli'' is designed to work successively as follows: (1) ''Bee. coli'' continuously secretes mannosidase to inhibit the sprouting of N. ceranae spores. (2) if the bee is infected with ''N. ceranae'', the fungus-killing-circuit with a positive feedback design will be turned on to wipe out ''N. ceranae''. (3) if these designer weapons should fail to conquer ''N. ceranae'', a bee-suicide-operon will be activated to kill the infected bees but save their companions.
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Besides, a light-inducible lysis system is created to ensure our ''Bee. coil'' only lives inside of the bee. In addition, we have used encapsulation as the method to send our ''Bee. coli'' into the bee. Since the capsule will only dissolve in a bee’s gut, our ''Bee. coli'' will not wantonly spread out.
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[[File:NYMU_project_overview.png|900px|center|link=https://2013.igem.org/Team:NYMU-Taipei/Project/Overview]]
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/*======
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==[https://2013.igem.org/Jamborees-Asia Our 2013 iGEM Awards]==
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======*/
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===☆ Finalist===
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</style>
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===☆ Best New BioBrick Part or Device, Engineered===
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<script>
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[[File:NYMU_we're_the_winnner.png|800px|center]]
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jQuery(document).ready(function($){
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//eliminate jsnotice
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==List of Our Experimental Accomplishments==
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[https://2013.igem.org/Team:NYMU-Taipei/Experiment/Wet_Lab ✓ 23 new BioBricks to part registry]
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[https://2013.igem.org/Team:NYMU-Taipei/Project/Enter ✓ A way to transport genetic modified ''E. coli'']
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/*epic box info functionality*/
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//small icons
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[https://2013.igem.org/Team:NYMU-Taipei/Project/safe ✓ A light-induced lysis system for safety]
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}
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</script>
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</head>
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<body>
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[https://2013.igem.org/Team:NYMU-Taipei/Project/Inhibition/Sensor ✓ The improvement of BioBrick Part AhpCp]
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<div id="box1" align="justify">
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[https://2013.igem.org/Team:NYMU-Taipei/Modeling/Overview ✓ Modeling standard for prescription of engineered ''E. coli'']
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<a href=" ">
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</a>
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<h2>CCD Preventing Bacteria</h2>
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<p></p>
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<p></p>
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[https://2013.igem.org/Team:NYMU-Taipei/Modeling/Ethanol ✓ An inducible delay positive feedback circuit]
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<div class="threeboxes">
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[https://2013.igem.org/Team:NYMU-Taipei/HumanPractice/HumCollab ✓ Help NTU-Taida iGEM team characterize their BioBrick devices]
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<img src="https://static.igem.org/mediawiki/2012/0/02/UCalgary2012_ThreeBoxMusic.png"></img>
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<h2>iGEM Style!</h2>
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<h2>Synergy</h2>
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<img src="https://static.igem.org/mediawiki/2012/b/b1/UCalgary2012_ThreeBoxFilm.png"></img>
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<h2>Intro Video</h2>
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<!--ZE EPIC BOX-->
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[https://2013.igem.org/Team:NYMU-Taipei/HumanPractice/HumFlows ✓ Video documentations of performing experimental procedures]
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[https://2013.igem.org/Team:NYMU-Taipei/HumanPractice/HumPracticalApp ✓ Cooperation with beekeepers]
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<p>We took the initiative with the oil sands industry and established a dialogue between industry experts, academics, and government representatives. Through these talks a roadmap for the use of synthetic biology in the oil sands was established, focusing on biosensing and bioremediation.</p>
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<p>FRED is our <b>F</b>unctional, <b>R</b>obust <b>E</b>lectrochemical <b>D</b>etector. FRED is responsible for detecting and measuring naphthenic acids (NAs) and is able to produce an electrochemical signal that can be measured. FRED can be used to measure toxins in tailings pond samples within minutes, without having to ship them to an off-site lab for testing. Click on FRED to learn more!</p>
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<p>OSCAR is our <b>O</b>ptimized <b>S</b>ystem for <b>C</b>arboxylic <b>A</b>cid <b>R</b>emediation. OSCAR is responsible for converting toxins such as catechol and naphthenic acids into hydrocarbons. OSCAR is also capable of removing nitrogen and sulfur groups to further purify the hydrocarbons produced. Click on OSCAR to learn more!</p>
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[https://2013.igem.org/Team:NYMU-Taipei/Project/Inhibition/Id-Nosema ✓ Primers for identifying Nosema]
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Latest revision as of 02:41, 29 October 2013

National Yang Ming University
Taipei, Taiwan

  • Home
  • Team
  • Project
    Overview Entering of Bee.coli Prohibiting Sprouting Inhibiting Infection Sensing Nosema Killing Nosema Circuit Suicide Solution eco-friendly e.coli Identifying Nosema
  • experiment
    Protocols Data Notes
  • Modeling
    Overview Sensors Main Parts Ethanol Model Epidemic Model
  • Human Practice
    Overview Outreach Collaborations Flows Built-up Practical Applications
  • Safety

FlexSlider 2

Contents

  • 1 Overview of 2013 NYMU iGEM Team Project
  • 2 Our 2013 iGEM Awards
    • 2.1 ☆ Finalist
    • 2.2 ☆ 1st runner up
    • 2.3 ☆ Best Presentation
    • 2.4 ☆ Best Parts Collection
    • 2.5 ☆ Most Improved Registry Part
    • 2.6 ☆ Best New BioBrick Part or Device, Engineered
  • 3 List of Our Experimental Accomplishments

Overview of 2013 NYMU iGEM Team Project

To save bees from Nosema ceranae infection, the culprit of colony collapse disorder (CCD), NYMU-Taipei iGEM team has created the so-called Bee. coli from Escherichia coli MG1655, which naturally resides in bees. The Bee. coli is designed to work successively as follows: (1) Bee. coli continuously secretes mannosidase to inhibit the sprouting of N. ceranae spores. (2) if the bee is infected with N. ceranae, the fungus-killing-circuit with a positive feedback design will be turned on to wipe out N. ceranae. (3) if these designer weapons should fail to conquer N. ceranae, a bee-suicide-operon will be activated to kill the infected bees but save their companions.

Besides, a light-inducible lysis system is created to ensure our Bee. coil only lives inside of the bee. In addition, we have used encapsulation as the method to send our Bee. coli into the bee. Since the capsule will only dissolve in a bee’s gut, our Bee. coli will not wantonly spread out.

NYMU project overview.png

Our 2013 iGEM Awards

I'm the winner.png

☆ Finalist

☆ 1st runner up

☆ Best Presentation

☆ Best Parts Collection

☆ Most Improved Registry Part

☆ Best New BioBrick Part or Device, Engineered

NYMU we're the winnner.png

List of Our Experimental Accomplishments

✓ 23 new BioBricks to part registry

✓ A way to transport genetic modified E. coli

✓ A light-induced lysis system for safety

✓ The improvement of BioBrick Part AhpCp

✓ Modeling standard for prescription of engineered E. coli

✓ An inducible delay positive feedback circuit

✓ Help NTU-Taida iGEM team characterize their BioBrick devices

✓ Video documentations of performing experimental procedures

✓ Cooperation with beekeepers

✓ Primers for identifying Nosema

Retrieved from "http://2013.igem.org/Team:NYMU-Taipei"
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