Team:Fudan-Shanghai/Project
From 2011.igem.org
Line 12: | Line 12: | ||
<table border=10 bordercolor=#CEFFCE bgcolor=#CEFFCE width=950 cellpadding=10 cellspacing=0> | <table border=10 bordercolor=#CEFFCE bgcolor=#CEFFCE width=950 cellpadding=10 cellspacing=0> | ||
<tr height=50 bgcolor=#CEFFCE> | <tr height=50 bgcolor=#CEFFCE> | ||
- | <td colspan=2><h1><img src="https://static.igem.org/mediawiki/2011/e/ee/Fudan_Etree.jpg " alt="E.tree" width=100 align=center hspace=20> E.Tree </h1></td> | + | <td colspan=2><h1><img src="https://static.igem.org/mediawiki/2011/e/ee/Fudan_Etree.jpg " alt="E.tree" width=100 align=center hspace=20> Part I: E.Tree </h1></td> |
</tr> | </tr> | ||
- | <tr height= | + | <tr height=300 > |
<td rowspan=2 bgcolor=#FFFFCE width=400 ><h1>Detail:</h1><font size=3> | <td rowspan=2 bgcolor=#FFFFCE width=400 ><h1>Detail:</h1><font size=3> | ||
The project “E.tree” is consisted of two genetically modified E.coli: E. trunk and E.leaf. <br><br> | The project “E.tree” is consisted of two genetically modified E.coli: E. trunk and E.leaf. <br><br> | ||
- | + | E.trunk detects nitrates in the medium; if KNO3 is present, the first circuit is activated, RhlI produces the AHL (C4-homoserine lactone) and TetR is synthesized to block the second pathway. If the medium lacks KNO3, the first pathway is off while the second pathway is activated and LasI produces an AHL autoinducer (3OC12-homoserine lactone). <br><br> | |
- | E.trunk detects nitrates in the medium; if KNO3 is present, the first circuit is activated, RhlI produces the AHL (C4-homoserine lactone) and TetR is synthesized to block the second pathway. If the medium lacks KNO3, the first pathway is off while the second pathway is activated and LasI produces an AHL autoinducer (3OC12-homoserine lactone). | + | E.leaf changes color corresponding to the signal molecules released by E.trunk. RhlR synthesized in E.leaf binds to the RhlI-directed signal, and the complex then interact with the pRhl promoter and yellow pigment is produced. This circuit also encodes RhlI, which multiple the circuit, so that all E.leaf would turn yellow. Similarly, if E.trunk releases 3OC12-homoserine lactone, which is encodes by LasI, all “leaves” would turn green. <br><br> |
- | <br><br> | + | </font></td> |
- | E.leaf changes color corresponding to the signal molecules released by E.trunk. RhlR synthesized in E.leaf binds to the RhlI-directed signal, and the complex then interact with the pRhl promoter and yellow pigment is produced. This circuit also encodes RhlI, which multiple the circuit, so that all E.leaf would turn yellow. Similarly, if E.trunk releases 3OC12-homoserine lactone, which is encodes by LasI, all “leaves” would turn green. | + | <td bgcolor=#CEFFCE alain=center><img src="https://static.igem.org/mediawiki/2011/a/a9/E.tree_detail.JPG" height=300</td> |
- | <br><br> | + | |
- | </font></td> | + | |
- | <td bgcolor=#CEFFCE></td> | + | |
</tr> | </tr> | ||
Revision as of 09:14, 4 October 2011
Part I: E.Tree |
|
Detail:The project “E.tree” is consisted of two genetically modified E.coli: E. trunk and E.leaf.E.trunk detects nitrates in the medium; if KNO3 is present, the first circuit is activated, RhlI produces the AHL (C4-homoserine lactone) and TetR is synthesized to block the second pathway. If the medium lacks KNO3, the first pathway is off while the second pathway is activated and LasI produces an AHL autoinducer (3OC12-homoserine lactone). E.leaf changes color corresponding to the signal molecules released by E.trunk. RhlR synthesized in E.leaf binds to the RhlI-directed signal, and the complex then interact with the pRhl promoter and yellow pigment is produced. This circuit also encodes RhlI, which multiple the circuit, so that all E.leaf would turn yellow. Similarly, if E.trunk releases 3OC12-homoserine lactone, which is encodes by LasI, all “leaves” would turn green. |
|