Difference between revisions of "Team:Kent"

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These magnetic nanoparticles are grown from iron inside of organelle-like structures called magnetosomes.
 
These magnetic nanoparticles are grown from iron inside of organelle-like structures called magnetosomes.
In this project, we will produce magnetite nanoparticles using a synthetic biology approach utilising enzymes involved in magnetosome formation. We will utilise proteins MamP, MamT and MamX, which were chosen due to their proposed involvement in promoting magnetite crystal maturation in <i>M. gryphiswaldense</i>.</div>
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In this project, we will produce magnetite nanoparticles using a synthetic biology approach utilising enzymes involved in magnetosome formation. We will utilise proteins MamP, MamT and MamX, which were chosen due to their proposed involvement in promoting magnetite crystal maturation in <i>M. gryphiswaldense</i>. The proteins will also be purified and tested <i>in vitro</i>. </div>
  
  
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Each of the genes will be incorporated both separately and as a set into <i>E. coli</i> with the aim of producing magnetite crystals in vivo in the cells.
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The proteins will also be purified and tested <i>in vitro</i>. Our results will further our understanding of how bacteria cells are able to form and organise magnetite nanoparticles in magnetosomes, and demonstrate how synthetic biology approach can be used to make nano-materials.
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Our results will further our understanding of how bacteria cells are able to form and organise magnetite nanoparticles in magnetosomes, and demonstrate how synthetic biology approach can be used to make nano-materials.
 
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Revision as of 20:54, 12 August 2016

Mag-nano-tite: Creating magnetite nanoparticles in E.coli

Bacteria such as Magnetospirillum gryphiswaldense grow magnetite nano-crystals that they use for orientation.
These magnetic nanoparticles are grown from iron inside of organelle-like structures called magnetosomes. In this project, we will produce magnetite nanoparticles using a synthetic biology approach utilising enzymes involved in magnetosome formation. We will utilise proteins MamP, MamT and MamX, which were chosen due to their proposed involvement in promoting magnetite crystal maturation in M. gryphiswaldense. The proteins will also be purified and tested in vitro.
Our results will further our understanding of how bacteria cells are able to form and organise magnetite nanoparticles in magnetosomes, and demonstrate how synthetic biology approach can be used to make nano-materials.




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