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Team:Chiba
From 2013.igem.org
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<h2>Abstract</h2> | <h2>Abstract</h2> | ||
| - | <p> In nature, there exists a variety of magnetotactic bacteria. Recently, it was reported that non-magnetotactic cells such as yeast can be magnetized to some extent. We set the goal to transform <i>E. coli</i> into those that are attracted by magnets. By magnetizing <i>E. coli</i>, the cell harvesting process will be much simpler and more economical than the conventional processes such as centrifugation and filtration. To this end, we are conducting three itemized projects. (1) modification of iron transportation network to import as much Fe ions as possible in <i>E. coli</i>, (2) sequestering/ storing iron into human ferritin, and (3) converting cytosolic space from reducing to oxidizing in order to elevate Fe(II)/ Fe(III) ratio within. Because all such manipulations significantly impact the physiology of the host cell, we are establishing the BioBrick platform that enables the temporal knockdown of multiple genes using recently control technology such as CRISPRi. | + | <p> In nature, there exists a variety of magnetotactic bacteria. Recently, it was reported that non-magnetotactic cells such as yeast can be magnetized to some extent. We set the goal to transform <i>E. coli</i> into those that are attracted by magnets. By magnetizing <i>E. coli</i>, the cell harvesting process will be much simpler and more economical than the conventional processes such as centrifugation and filtration. To this end, we are conducting three itemized projects. (1) modification of iron transportation network to import as much Fe ions as possible in <i>E. coli</i>, (2) sequestering/ storing iron into human ferritin, and (3) converting cytosolic space from reducing to oxidizing in order to elevate Fe(II)/ Fe(III) ratio within. Because all such manipulations significantly impact the physiology of the host cell, we are establishing the BioBrick platform that enables the temporal knockdown of multiple genes using recently control technology such as CRISPRi.</p> |
<center><img src="https://static.igem.org/mediawiki/2013/f/f3/Chiba_home.jpg"></center> | <center><img src="https://static.igem.org/mediawiki/2013/f/f3/Chiba_home.jpg"></center> | ||
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<h2>Sponsors</h2> | <h2>Sponsors</h2> | ||
Revision as of 16:02, 27 September 2013
Welcome to Chiba wiki!!
We return to iGem after an absence of three years.Summer is too hot season,but we are hotter than summer.So we have passion.
Abstract
In nature, there exists a variety of magnetotactic bacteria. Recently, it was reported that non-magnetotactic cells such as yeast can be magnetized to some extent. We set the goal to transform E. coli into those that are attracted by magnets. By magnetizing E. coli, the cell harvesting process will be much simpler and more economical than the conventional processes such as centrifugation and filtration. To this end, we are conducting three itemized projects. (1) modification of iron transportation network to import as much Fe ions as possible in E. coli, (2) sequestering/ storing iron into human ferritin, and (3) converting cytosolic space from reducing to oxidizing in order to elevate Fe(II)/ Fe(III) ratio within. Because all such manipulations significantly impact the physiology of the host cell, we are establishing the BioBrick platform that enables the temporal knockdown of multiple genes using recently control technology such as CRISPRi.
Sponsors
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