Team:Berlin/Project

From 2014.igem.org

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     <h2 class="green-text">STEPS OF PRODUCING E.COLI</h2>
     <h2 class="green-text">STEPS OF PRODUCING E.COLI</h2>
     <div class="row project-steps top">
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>1</span><img src="https://static.igem.org/mediawiki/2014/b/b4/Team_Berlin_project_04.png"/></div><p>Knocking out the iron efflux transporter gene FieF and the iron uptake suppressor Fur to increase the total iron level of the cytosol.</p></div>
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>1</span><img src="img/project/Team_Berlin_project_04.png"/></div><p>Knocking out the iron efflux transporter gene FieF and the iron uptake suppressor Fur to increase the total iron level of the cytosol.</p></div>
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>2</span><img src="https://static.igem.org/mediawiki/2014/3/31/Team_Berlin_project_02.png"/></div><p>Sequestering iron in a ferritin protein.</p></div>
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>2</span><img src="img/project/Team_Berlin_project_02.png"/></div><p>Sequestering iron in a ferritin protein.</p></div>
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>3</span><img src="https://static.igem.org/mediawiki/2014/a/a7/Team_Berlin_project_03.png"/></div><p>Iron crystals are formed and the cell is detoxified.</p></div>
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>3</span><img src="img/project/Team_Berlin_project_03.png"/></div><p>Iron crystals are formed and the cell is detoxified.</p></div>
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>4</span><img src="https://static.igem.org/mediawiki/2014/5/50/Team_Berlin_project_01.png"/></div><p>Create crystals by using intensive high-throughput growth medium optimization to discover the best conditions for the formation of magnetic nanoparticles in E. coli.</p></div>
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       <div class="col-md-6" style="padding-bottom:20px;"><div class="project-steps-img"><span>4</span><img src="img/project/Team_Berlin_project_01.png"/></div><p>Create crystals by using intensive high-throughput growth medium optimization to discover the best conditions for the formation of magnetic nanoparticles in E. coli.</p></div>
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Revision as of 17:55, 5 October 2014

WHAT´S HAPPENING?

As previous iGEM teams have shown, synthesizing fully functional magnetosomes in E. coli is highly difficult as more than 60 highly regulated genes are involved. As a more feasible alternative, we simply want to synthesize magnetic nanoparticles in E. coli in order to attract cells with strong magnetic fields.
Therefore we want to use different strategies including manipulation of the iron homeostasis of E. coli, expression of different metal binding proteins such as ferritins and metallothioneins as well as a high-throughput growth medium optimization.

Furthermore, we will work with other metal binding proteins such as metallothioneins and phytochelatin synthases in order to achieve nanoparticle synthesis. Once we have discovered the best way to magnetize E. coli bacteria, we will build and characterize suitable BioBricks that can be used by any research lab or iGEM team in the world in order to remote control the cellular movement.


STEPS OF PRODUCING E.COLI

1

Knocking out the iron efflux transporter gene FieF and the iron uptake suppressor Fur to increase the total iron level of the cytosol.

2

Sequestering iron in a ferritin protein.

3

Iron crystals are formed and the cell is detoxified.

4

Create crystals by using intensive high-throughput growth medium optimization to discover the best conditions for the formation of magnetic nanoparticles in E. coli.

Müller-Breslau-Str. 10
10623 Berlin
Phone: +49 1778800244
Mail: mail@igem.berlin
©2014 iGem Berlin, Layout/Umsetzung: Valerian Blos, Marius Wessel

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