Team:Macquarie Australia/trial

From 2012.igem.org

(Difference between revisions)
Line 96: Line 96:
<li>Heme oxygenase</li>
<li>Heme oxygenase</li>
</ol>  
</ol>  
-
The bacteriophytochromes from <i>Deinococcus radiodurans</i> and <i>Agrobacterium tumefaciens</i> were chosen. </div>
+
The bacteriophytochromes from <i>Deinococcus radiodurans</i> and <i>Agrobacterium tumefaciens</i> were chosen. Over the next week Matt Stclair started to develop the G-blocks by:
 +
<ol>
 +
<li>Acquiring the DNA sequence</li>
 +
<li>Translate into protein sequence </li>
 +
<li>Using the DNA sequence, optimise codon usage for <i>E. coli</i></li>
 +
<li>Translate into protein sequence and ensure no changes in amino acids relative to the original sequence </li>
 +
</ol>
 +
</div>
<img src="https://static.igem.org/mediawiki/2012/8/85/Protocol_content_bottom.png" id="bot-part"></img>
<img src="https://static.igem.org/mediawiki/2012/8/85/Protocol_content_bottom.png" id="bot-part"></img>
</div>
</div>

Revision as of 04:45, 14 September 2012



To browse through our notebook simply click on the image with the date. It will expand with what we did that week. To continue on simply click on the next one.
Week 1- Tuesday July 31st

With the break between semester over the Macquarie iGEM returned to classes. For us this was the first day of iGEM 2012. We had our first meeting and discussed our project. Dr. Louise Brown and Associate Professor Rob Willows were introduced the team and we were began to determine who would take on certain roles within the team

Gibson Cloning was introduced to all of us for the first time and we eagerly began our project. We had decided to develop a gene-switch controlled by light. To do this a couple of genes would be needed:

  1. a bacteriophytochrome
  2. Heme oxygenase
The bacteriophytochromes from Deinococcus radiodurans and Agrobacterium tumefaciens were chosen. Over the next week Matt Stclair started to develop the G-blocks by:
  1. Acquiring the DNA sequence
  2. Translate into protein sequence
  3. Using the DNA sequence, optimise codon usage for E. coli
  4. Translate into protein sequence and ensure no changes in amino acids relative to the original sequence
2

This is a trial. I do not know if this is going to work or not!

3

This is a trial. I do not know if this is going to work or not!

4

This is a trial. I do not know if this is going to work or not!

5

This is a trial. I do not know if this is going to work or not!

6

This is a trial. I do not know if this is going to work or not!

7

This is a trial. I do not know if this is going to work or not!

7

This is a trial. I do not know if this is going to work or not!

7

This is a trial. I do not know if this is going to work or not!







Retrieved from "http://2012.igem.org/Team:Macquarie_Australia/trial"