Revision as of 23:08, 3 October 2012

British Columbia - 2012.igem.org

Biodesulfurization HPLC

1. Grow overnight cultures of cells containing dsz operon in 5mL culture of LB.

2. Measure O.D 600 with a spectrometer. Inoculate in 200mL culture of LB in a 500mL flask such that the starting O.D 600 is 0.05.

3. Incubate at 37°C shaking at 200rpm.

4. Extract 25mL at O.D 600 intervals of 0.3, 0.7, and 1.0.

5. Spin down cells using a centrifuge (1600g, 10min) and extract 25mL of supernatant.

6. Acidify supernatant to pH of 2.0 with 6N HCl to inactivate enzymes.

7. Extract with equal volume of ethyl acetate.

8. Dry extract with nitrogen gas and re-suspend in mobile phase with 80% acetonitrile.

9. Filter extract resuspended in acetonitrile using reverse phase chromatography and C-18 column.

10. Elute mobile phase at a flow rate of 0.8 ml/min and peaks of DBT were detected at 280nm by HPLC.

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+<h1>Biodesulfurization HPLC</h1>
+. Grow overnight cultures of cells containing dsz operon in 5mL culture of LB.
+. Measure O.D 600 with a spectrometer. Inoculate in 200mL culture of LB in a 500mL flask such that the starting O.D 600 is 0.05.
+. Incubate at 37°C shaking at 200rpm.
+. Extract 25mL at O.D 600 intervals of 0.3, 0.7, and 1.0.
+. Spin down cells using a centrifuge (1600g, 10min) and extract 25mL of supernatant.
+. Acidify supernatant to pH of 2.0 with 6N HCl to inactivate enzymes.
+. Extract with equal volume of ethyl acetate.
+. Dry extract with nitrogen gas and re-suspend in mobile phase with 80% acetonitrile.
+. Filter extract resuspended in acetonitrile using reverse phase chromatography and C-18 column.
+. Elute mobile phase at a flow rate of 0.8 ml/min and peaks of DBT were detected at 280nm by HPLC.