Team:Calgary/Notebook/Protocols/Modelvalidation
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<p> After running the model for the pathway in question, the PetroBrick (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K590025">BBa_K590025</a></b>), overnight cultures were made adding different combinations of metabolites found to increase product output from the model. </p> | <p> After running the model for the pathway in question, the PetroBrick (<b><a href="http://partsregistry.org/wiki/index.php?title=BBa_K590025">BBa_K590025</a></b>), overnight cultures were made adding different combinations of metabolites found to increase product output from the model. </p> | ||
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+ | <ol> | ||
+ | <li>PetroBrick culture was grown in 3x 20mL cultures from isolated plate colonies supplemented with 50 ug/mL chloramphenicol. These cultures were grown overnight at 37<sup>o</sup>C with shaking. | ||
+ | <li>Culture tubes had 5 mL of minimal M9 media with 1% (w/v) filter sterilized glucose, and 50 ug/mL chloramphenicol added to each tube. | ||
+ | <li>All chemicals added were at a concentration of 50 mM except for AMP (100 mg/L) and L-aspartate (100mg/L). Stocks were dissolved in water at concentrations ~100x what was being added (provided that the compound was soluble) to ensure that changes in volume would not account for differences seen. | ||
+ | <li>Cells were allowed to grow for 72 hours at 37<sup>o</sup>C with shaking. | ||
+ | <li>Cultures then had OD<sub>600</sub> readings taken to normalize against. | ||
+ | <li>Cultures were then sonicated with a Misonix Cell Disruptor at Dial 11 (output of 18 watts) for 1 min. | ||
+ | <li>1 mL of ethyl acetate was added to each tube shaken vigorously and spun down at 4000 RPM for 5 min. at 4<sup>o</sup>C | ||
+ | <li>250 uL of the ethyl acetate layer was ran onto the GC/MS (see other protocol). | ||
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Revision as of 00:50, 4 October 2012
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Modelling Validation Experiments
After running the model for the pathway in question, the PetroBrick (BBa_K590025), overnight cultures were made adding different combinations of metabolites found to increase product output from the model.
- PetroBrick culture was grown in 3x 20mL cultures from isolated plate colonies supplemented with 50 ug/mL chloramphenicol. These cultures were grown overnight at 37oC with shaking.
- Culture tubes had 5 mL of minimal M9 media with 1% (w/v) filter sterilized glucose, and 50 ug/mL chloramphenicol added to each tube.
- All chemicals added were at a concentration of 50 mM except for AMP (100 mg/L) and L-aspartate (100mg/L). Stocks were dissolved in water at concentrations ~100x what was being added (provided that the compound was soluble) to ensure that changes in volume would not account for differences seen.
- Cells were allowed to grow for 72 hours at 37oC with shaking.
- Cultures then had OD600 readings taken to normalize against.
- Cultures were then sonicated with a Misonix Cell Disruptor at Dial 11 (output of 18 watts) for 1 min.
- 1 mL of ethyl acetate was added to each tube shaken vigorously and spun down at 4000 RPM for 5 min. at 4oC
- 250 uL of the ethyl acetate layer was ran onto the GC/MS (see other protocol).