Team:Jilin China/DESIGN

From 2014.igem.org

(Difference between revisions)
Line 209: Line 209:
<div id="coop">
<div id="coop">
<center><h3>How to find and degradation of microcystins LR?</h3></center>
<center><h3>How to find and degradation of microcystins LR?</h3></center>
-
<div style="margin:0 auto;"><img style="height:117px;" src="https://static.igem.org/mediawiki/2014/1/14/Design1.jpg"><img height="116" src="https://static.igem.org/mediawiki/2014/4/44/Design3.jpg"><br></div>
+
<p><img style="height:117px;" src="https://static.igem.org/mediawiki/2014/1/14/Design1.jpg"><img height="116" src="https://static.igem.org/mediawiki/2014/4/44/Design3.jpg"><br>
-
   <p>Microcystin-LR (MC-LR) is a naturally occurring  toxin released after the algal cells break down, which can do great damage to  liver,very stable and in some extent is very resistant to high temperature and  pH change, so it brings the water purification into a very embarrassing  situation. <br>
+
   Microcystin-LR (MC-LR) is a naturally occurring  toxin released after the algal cells break down, which can do great damage to  liver,very stable and in some extent is very resistant to high temperature and  pH change, so it brings the water purification into a very embarrassing  situation. <br>
   Mlr promoter is able to detect whether  water containing microcystin LR and start to expressthe GFP-mlrA fusion protein.  GFP can emit green fluorescence, very simple and very sensitive to tell us the  water contains toxic microcystin LR. MlrA can directly degrade microcystin  LRand eliminate its toxicity, eliminate the toxins in water pollution.<br>
   Mlr promoter is able to detect whether  water containing microcystin LR and start to expressthe GFP-mlrA fusion protein.  GFP can emit green fluorescence, very simple and very sensitive to tell us the  water contains toxic microcystin LR. MlrA can directly degrade microcystin  LRand eliminate its toxicity, eliminate the toxins in water pollution.<br>
   The mlr promoter-GFP-mlrA was be cloned  into the <em>E. coli-L. lactis</em> shuttle  expression vector pMG36e, so it can be able to express in E. coli and <em>Lactococcus lactis</em>, which Can easily be  constructed in the laboratory, at the same time to avoid secondary pollution in  the natural environment of <em>E. coli</em>.<br>
   The mlr promoter-GFP-mlrA was be cloned  into the <em>E. coli-L. lactis</em> shuttle  expression vector pMG36e, so it can be able to express in E. coli and <em>Lactococcus lactis</em>, which Can easily be  constructed in the laboratory, at the same time to avoid secondary pollution in  the natural environment of <em>E. coli</em>.<br>

Revision as of 02:32, 18 October 2014

Welcome!
Team Jilin_China

How to find and degradation of microcystins LR?


Microcystin-LR (MC-LR) is a naturally occurring toxin released after the algal cells break down, which can do great damage to liver,very stable and in some extent is very resistant to high temperature and pH change, so it brings the water purification into a very embarrassing situation.
Mlr promoter is able to detect whether water containing microcystin LR and start to expressthe GFP-mlrA fusion protein. GFP can emit green fluorescence, very simple and very sensitive to tell us the water contains toxic microcystin LR. MlrA can directly degrade microcystin LRand eliminate its toxicity, eliminate the toxins in water pollution.
The mlr promoter-GFP-mlrA was be cloned into the E. coli-L. lactis shuttle expression vector pMG36e, so it can be able to express in E. coli and Lactococcus lactis, which Can easily be constructed in the laboratory, at the same time to avoid secondary pollution in the natural environment of E. coli.


Top

Retrieved from "http://2014.igem.org/Team:Jilin_China/DESIGN"