Team:Utah State

From 2009.igem.org

(Difference between revisions)
Line 32: Line 32:
       </br>
       </br>
       <font size="2" face="Helvetica, Arial, San Serif" color =#222222>
       <font size="2" face="Helvetica, Arial, San Serif" color =#222222>
-
               Investigating a multi-host BioBrick vector and secretion of cellular products
+
               Investigating a multi-host BioBrick vector and secretion of cellular products</br>
 +
            <p> In the interest of creating a universal BioBrick vector, the goal of our project is to improve, modify, and test the broad-host vector pRL 1383a. After ensuring that the vector functions properly, we will test in the cyanobacterium Synechocystis, Pseudomonas putida, and Escherichia coli.  We will then develop expression systems in Synechocystis to produce various proteins. </p>
       </font>
       </font>
 +
   
     </td>
     </td>
      
      
Line 42: Line 44:
</html>
</html>
-
''In the interest of creating a universal BioBrick vector, the goal of our project is to improve, modify, and test the broad-host vector pRL 1383a. After ensuring that the vector functions properly, we will test in the cyanobacterium Synechocystis, Pseudomonas putida, and Escherichia coli.  We will then develop expression systems in Synechocystis to produce various proteins. ''
+
 
<html>
<html>
<head>
<head>

Revision as of 06:14, 9 October 2009

USUlogo.jpg
Home The Team The Project Parts Notebook Protocols Links Practice


BioBricks without Borders:
Investigating a multi-host BioBrick vector and secretion of cellular products

In the interest of creating a universal BioBrick vector, the goal of our project is to improve, modify, and test the broad-host vector pRL 1383a. After ensuring that the vector functions properly, we will test in the cyanobacterium Synechocystis, Pseudomonas putida, and Escherichia coli. We will then develop expression systems in Synechocystis to produce various proteins.