Team:Cornell

From 2011.igem.org

(Difference between revisions)
Line 11: Line 11:
<div style="text-align: center;"><big><big><big><a href="www.google.com">Click
<div style="text-align: center;"><big><big><big><a href="www.google.com">Click
for Recruting</a><a href="www.google.com">!</a><br><br>
for Recruting</a><a href="www.google.com">!</a><br><br>
-
</big></big></big></div>
+
</big></big></big></div>[[Team:Cornell/Recruiting| Sponsors]
<table
<table
style="text-align: left; height: 375px; background-color: rgb(215, 205, 159); margin-left: auto; margin-right: auto; width: 925px;"
style="text-align: left; height: 375px; background-color: rgb(215, 205, 159); margin-left: auto; margin-right: auto; width: 925px;"

Revision as of 02:12, 26 October 2011



Home Table
Click for Recruting!

[[Team:Cornell/Recruiting| Sponsors]

Abstract

Cornell’s 2011 iGEM team has designed a new, scalable, and cell-free method to produce complex biomolecules. Current methods for purification from cellular lysate are expensive and time consuming. Biofactory utilizes modified enzymes, capable of being attached to surfaces, in the creation of a modular microfluidic chip for each enzyme. The surface bonding is performed by the well-characterized biotin-avidin mechanism. When combined in series, these chips operate as a linear biochemical pathway for continuous flow reactions. Additionally, we plan to engineer E. coli with the mechanism for light-induced apoptosis to easily lyse cultures producing the necessary enzymes. The resulting lysate is flowed through the microfluidic channels, coating them with the desired enzyme. We believe this chemical synthesis method will reduce unwanted side reactions and lower the costs of producing bio-pharmaceuticals in the future.


Project Data
Team Multimedia