Team:Calgary/Notebook/Protocols/escapersassay

From 2012.igem.org

(Difference between revisions)
(Created page with "{{Team:Calgary/TemplateNotebookOrange| TITLE=Glycine Assay Protocols| CONTENT = <html> <p> Three glycine assays were performed in order to better characterize the <i>glyA</i> K...")
Line 1: Line 1:
{{Team:Calgary/TemplateNotebookOrange|
{{Team:Calgary/TemplateNotebookOrange|
-
TITLE=Glycine Assay Protocols|
+
TITLE=Escaper assay for the rhamnose system|
CONTENT = <html>
CONTENT = <html>
-
<p> Three glycine assays were performed in order to better characterize the <i>glyA</i> Keio Knockout Strain (JW2535-1).  These included an assay to determine the minimal amount of glycine required for survival of the auxotroph in minimal media which was used in previous Petrobrick assays. Additionally, the functionality of the Petrobrick was evaluated in this strain to see if similar concentrations of hydrocarbons could be produced as in WT strains of <i>E. coli</i>. In order to evaluate if this strain could be used in conjunction with our kill switch mechanisms, we used these systems in conjunction.
+
<p>The following assay is based on CFU in both Top 10 and glyA knockout of <i>E. coli</i>.</p>
-
 
+
-
<h2>Media Optimization for the Glycine Auxotroph</h2>
+
<ul>
<ul>
<li>The <i>glyA</i> auxotroph was grown in LB media overnight at 37<sup>o</sup>C with shaking.
<li>The <i>glyA</i> auxotroph was grown in LB media overnight at 37<sup>o</sup>C with shaking.
Line 13: Line 11:
<li>Cells were grown at 37<sup>o</sup>C with shaking for 12 and 24 hours and OD<sub>600</sub> measurements were used to quantitate growth.
<li>Cells were grown at 37<sup>o</sup>C with shaking for 12 and 24 hours and OD<sub>600</sub> measurements were used to quantitate growth.
</ul>
</ul>
-
 
-
<h2>Glycine Auxotrophy Effect on Petrobrick Output</h2>
 
-
<p>The effect of the auxotroph on the output of the Petrobrick was determined as discussed in the flux balance analysis assay using 50 mM glycine. <a href="http://2012.igem.org/Team:Calgary/Notebook/Protocols/Modelvalidation">Click here</a> to view this protocol.
 
</html>
</html>
}}
}}

Revision as of 03:27, 27 October 2012

Hello! iGEM Calgary's wiki functions best with Javascript enabled, especially for mobile devices. We recommend that you enable Javascript on your device for the best wiki-viewing experience. Thanks!

Escaper assay for the rhamnose system

The following assay is based on CFU in both Top 10 and glyA knockout of E. coli.

  • The glyA auxotroph was grown in LB media overnight at 37oC with shaking.
  • Cells were washed in M9 minimal media two times and spun in between at 4,000 RPM at 4oC for 10 min. each time.
  • Finally, washed cells were subcultured into 5 mL of M9 minimal media supplemented with 1% (w/v) glucose and 50 ug/mL Kanamycin.
  • Cells were grown at 37oC with shaking for 12 and 24 hours and OD600 measurements were used to quantitate growth.