Team:TMU-Tokyo
From 2013.igem.org
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<caption>Project description</caption> | <caption>Project description</caption> | ||
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- | <td>In the iGEM, most teams have inserted their Biobrick parts or devices into the plasmids and use them. It is true that there are many good points to use plasmids, for instance, it is easy to do transformation, and it is convenient to use high copy plasmid when you want to get high gene expression amount. However, there are some bad points to use plasmids too. For example, when the reproduction starting point of plural plasmids are covered, it can’t put in E.coli at the same time. Also it is difficult to control genetic expression closely. | + | <td><p>In the iGEM, most teams have inserted their Biobrick parts or devices into the plasmids and use them. It is true that there are many good points to use plasmids, for instance, it is easy to do transformation, and it is convenient to use high copy plasmid when you want to get high gene expression amount. However, there are some bad points to use plasmids too. For example, when the reproduction starting point of plural plasmids are covered, it can’t put in <i>E.coli</i> at the same time. Also it is difficult to control genetic expression closely.<br> |
- | Therefore, in this year, our team tried to standardize a new method to inserted Biobrick parts or devices in a genome of E.coli and used them. Also we really inserted the device which we designed in a genome of E.coli according to our method and functionalized it. | + | Therefore, in this year, our team tried to standardize a new method to inserted Biobrick parts or devices in a genome of E.coli and used them. Also we really inserted the device which we designed in a genome of <i>E.coli</i> according to our method and functionalized it.</p> |
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<table class="imple" border="1" width="450" height="300"> | <table class="imple" border="1" width="450" height="300"> | ||
- | <tr><td> | + | <tr height="30"><td>Implementation ―Genomic Pythagorean Device-</td></tr> |
- | <tr><td></td></tr> | + | <tr height="200"><td><p> According to the system that we spoke in the right, we really inserted the device named “Genomic Pythagorean Device”, which we designed into a genome of <i>E.coli</i>. “Pythagorean Device” is very famous in Japan because Japanese famous educational TV program "Pythagorean Switch" introduces various Pythagorean Devices. They are known as "Rube Goldberg machines" in the US. Pythagorean Devices are deliberately over-engineered or overdone systems that perform very simple task in very complicated process, usually including some chain reactions. We constructed “Pythagorean Device” in <i>E.coli</i> genome with lambda phage recombination system "RED" </p></td></tr> |
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- | < | + | <h1>Sponsors</h1> |
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- | < | + | <h1>contact us!!</h1> |
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Revision as of 09:06, 23 September 2013
In the iGEM, most teams have inserted their Biobrick parts or devices into the plasmids and use them. It is true that there are many good points to use plasmids, for instance, it is easy to do transformation, and it is convenient to use high copy plasmid when you want to get high gene expression amount. However, there are some bad points to use plasmids too. For example, when the reproduction starting point of plural plasmids are covered, it can’t put in E.coli at the same time. Also it is difficult to control genetic expression closely. |
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