Team:Brown-Stanford/Lab/Protocols/CementationColumn
From 2011.igem.org
(Difference between revisions)
(2 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
- | {{:Team:Brown-Stanford/Templates/ | + | {{:Team:Brown-Stanford/Templates/Protocol}} |
== '''Biocementation Column''' == | == '''Biocementation Column''' == | ||
Line 5: | Line 5: | ||
=== '''Materials''' === | === '''Materials''' === | ||
- | * | + | *15 mL falcon tube |
- | * | + | *20 g of Lunar/Martian regolith per tube |
*A peristaltic pump | *A peristaltic pump | ||
*Two feet of rubber tubing, epoxy glue, fabric matting | *Two feet of rubber tubing, epoxy glue, fabric matting | ||
*Heat Lamp | *Heat Lamp | ||
- | * | + | *30 mL of S. pasteurii culture (OD600 1.2) |
=== '''Procedure''' === | === '''Procedure''' === |
Latest revision as of 18:17, 28 September 2011
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.