Difference between revisions of "Team:NYMU-Taipei/Part Collection"

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<h3>★  ALERT! </h3>
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<p>This page is used by the judges to evaluate your team for the <a href="https://2017.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2017.igem.org/Judging/Awards"> award listed above</a>. </p>
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<p> Delete this box in order to be evaluated for this medal criterion and/or award. See more information at <a href="https://2017.igem.org/Judging/Pages_for_Awards"> Instructions for Pages for awards</a>.</p>
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        <h1>Part Collection</h1>
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        <p>　　Our part collection included basic parts and composite parts. We focused on two aspects, one, nitrogen affinity protein for nitrogen starvation and two, pigment production in cyanobacteria. These two approaches were aimed to produce more energy from microalgae by <font class="mark_backbone">nitrogen starvation</font> and <font class="mark_backbone">artificial photosynthesis</font>. We also implemented <font class="mark_backbone">suicide mechanism</font> by combining holin and endolysin with nitrogen affinity protein in one construct for issues regarding biosafety. We successfully proved the function of nitrogen affinity protein, suicide mechanism and yellow pigment production in E. coli and cyanobacteria. We also set up a <font class="mark_backbone">transformation platform</font> for cyanobacteria with these new transformation parts and protocols. In conclusion, we proved our concept by this part collection from BBa_K2350000 to BBa_K2350025.
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        <p>Link: <a href="https://2017.igem.org/Team:NYMU-Taipei/Parts">Parts</a></p>
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<h1> Part Collection </h1>
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<p>Did your team make a lot of great parts? Is there a theme that ties all your parts together? Do you have more than 10 parts in this collection? Did you make a CRISPR collection, a MoClo collection, or a collection of awesome pigment parts? Describe your parts collection on this page, so the judges can evaluate you for the Best Part Collection award.</p>
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While you should put all the characterization information for your parts on the Registry, you are encouraged to explain how all your parts form a collection on this page.
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<h3>Best Part Collection Special Prize</h3>
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<p>Did your team make a lot of great parts? Is there a team that ties all your parts together? Do you have more than 10 parts in this collection? Did you make a CRISPR collection, a MoClo collection or a collection of awesome pigment parts? Tell the judges you should be evaluated for the Best Parts Collection award! To be eligible for this award, these parts must adhere to <a href="http://parts.igem.org/DNA_Submission">Registry sample submission guidelines</a> and have been sent to the Registry of Standard Biological Parts.
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If you have a collection of parts you wish to nominate your team for this <a href="https://2017.igem.org/Judging/Awards">special prize</a>, make sure you add your part numbers to your <a href="https://2017.igem.org/Judging/Judging_Form">judging form</a> and delete the box at the top of this page.</p>
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<h4>Note</h4>
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<p>This page should list all the parts in the collection your team made during your project. You must add all characterization information for your parts on the Registry. You should not put characterization information on this page.</p>
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Latest revision as of 16:00, 1 November 2017

HOME
PROJECT
Overview
Pigments
Nitrogen starvation
Modeling
Hardware
Contribution
Improvement
Demonstration
LABWORK
Parts
Safety
Notebook
HUMAN PRACTICES
Silver HP
Gold & Integrated HP
Collaborations
ABOUT US
AWARDS
Applied Design
Modeling
Measurement
Plant
Basic Parts
Composite Parts
Part Collection
Public Engagement
JUDGING FORM

CONTACT US

Email us: 2017igem.nymutaipei@gmail.com
Call us: 886-2-28267316
Facebook: NYMU iGEM Team

AFFILIATIONS & ACKNOWLEDGMENT

IGEM 2017
National Yang-Ming University
Special Thanks

Part Collection

　　Our part collection included basic parts and composite parts. We focused on two aspects, one, nitrogen affinity protein for nitrogen starvation and two, pigment production in cyanobacteria. These two approaches were aimed to produce more energy from microalgae by nitrogen starvation and artificial photosynthesis. We also implemented suicide mechanism by combining holin and endolysin with nitrogen affinity protein in one construct for issues regarding biosafety. We successfully proved the function of nitrogen affinity protein, suicide mechanism and yellow pigment production in E. coli and cyanobacteria. We also set up a transformation platform for cyanobacteria with these new transformation parts and protocols. In conclusion, we proved our concept by this part collection from BBa_K2350000 to BBa_K2350025.

Link: Parts