Team:SCU-China/Description
From 2014.igem.org
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<h3 class="panel-title">The genes in transmitter are shown in Figure 2</h3> | <h3 class="panel-title">The genes in transmitter are shown in Figure 2</h3> | ||
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- | <p>In the transmitter, there are 2 independent gene lines correspondingly. For the first line, we link the genes which could express the LuxR and RhlI proteins and then keep them under the control of pLux. For the second line, there are 3 genes (LasI, PpyS, and CinR) under the control of pCin. So you see, when the sensors are stimulated properly, the LuxI/Cinl/LuxI+Cinl are secreted by the sensors and the transimitter could express and secrete the RhlI/ PpyS+LasI/RhlI+PpyS+LasI respectively into media.</p></div>< | + | <p>In the transmitter, there are 2 independent gene lines correspondingly. For the first line, we link the genes which could express the LuxR and RhlI proteins and then keep them under the control of pLux. For the second line, there are 3 genes (LasI, PpyS, and CinR) under the control of pCin. So you see, when the sensors are stimulated properly, the LuxI/Cinl/LuxI+Cinl are secreted by the sensors and the transimitter could express and secrete the RhlI/ PpyS+LasI/RhlI+PpyS+LasI respectively into media.</p></div><div id="effector"> |
+ | <div class="panel panel-default"> | ||
+ | <div class="panel-heading"> | ||
+ | <h3 class="panel-title">The genes in effector are shown in Figure 3</h3> | ||
+ | </div> | ||
+ | <div class="panel-body"> | ||
+ | <img src="https://static.igem.org/mediawiki/2014/6/62/ScuCell_3.png"> | ||
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+ | </div> | ||
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- | Actually, there are several well-differentiated bacteria to execute different function in the effector group. Up to now, we design 3 bacterium colonies. The first colony, we make a constitutive promoter regulate the expression of RhlR and mRFP1 is under the control of pRhl. The second colony, we use a constitutive promoter expressing the ptrotein LasR and RhlR and the expressing of GFP is controlled by a multi-promoter which is activated by RhlI+RhlR but inactivated by LasI+LasR. As for the final colony, we use the new cell communication system we find in Photorhabdus luminescence. The protein PluR is expressed by a constitutive promoter and the amilcp (a kind of photopsin with green light) is controlled by pPlu.</p> | + | <p>Actually, there are several well-differentiated bacteria to execute different function in the effector group. Up to now, we design 3 bacterium colonies. The first colony, we make a constitutive promoter regulate the expression of RhlR and mRFP1 is under the control of pRhl. The second colony, we use a constitutive promoter expressing the ptrotein LasR and RhlR and the expressing of GFP is controlled by a multi-promoter which is activated by RhlI+RhlR but inactivated by LasI+LasR. As for the final colony, we use the new cell communication system we find in Photorhabdus luminescence. The protein PluR is expressed by a constitutive promoter and the amilcp (a kind of photopsin with green light) is controlled by pPlu.</p></div> |
</div></div> | </div></div> | ||
Revision as of 18:23, 16 October 2014