Team:Brown-Stanford/Lab/Protocols/CementationColumn

From 2011.igem.org

(Difference between revisions)
(Materials)
Line 1: Line 1:
{{:Team:Brown-Stanford/Templates/Main}}
{{:Team:Brown-Stanford/Templates/Main}}
-
 
+
<html>
 +
<div id="subHeader">
 +
<ul id="subHeaderList">
 +
<li><a href="/Team:Brown-Stanford/Team">Team</a></li>
 +
<li><a href="/Team:Brown-Stanford/Lab/Notebook">Notebook</a></li>
 +
<li id="active"><a href="#" id="current">Protocols</a></li>
 +
<li><a href="/Team:Brown-Stanford/Lab/Safety">Safety</a></li>
 +
</ul>
 +
</div>
 +
</html>
 +
{{:Team:Brown-Stanford/Templates/Content}}
== '''Biocementation Column''' ==
== '''Biocementation Column''' ==

Revision as of 17:40, 27 September 2011

Brown-Stanford
iGEM

Biocementation Column

Materials

  • 15 mL falcon tube
  • 20 g of Lunar/Martian regolith per tube
  • A peristaltic pump
  • Two feet of rubber tubing, epoxy glue, fabric matting
  • Heat Lamp
  • 30 mL of S. pasteurii culture (OD600 1.2)

Procedure

  • The columns were first prewet with 20 mL of sterile Bang media.
  • The bacteria culture was draw into the feed tube, and allowed to settle in the column overnight
  • Cementation solution (1.5 M equimolar urea and calcium chloride) was fed into the feed tube, which was then placed into a constant loop with the output tube
  • The column was heated for 5 days, and allowed to cycle.