Difference between revisions of "Part:BBa K206000:Characterization"
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==General Characterization Protocols== | ==General Characterization Protocols== | ||
− | # Inoculate 5mL LB-Chlor medium in a sterile test tube with a colony from a streak plate of pSB1C3- | + | # Inoculate 5mL LB-Chlor medium in a sterile test tube with a colony from a streak plate of pSB1C3-K206002-transformed BW27783 cells. |
# Grow overnight at 37C, shaking at 210rpm. | # Grow overnight at 37C, shaking at 210rpm. | ||
# Measure OD600 and dilute to OD600=0.25A in 15mL of LB-Chlor with added arabinose (or other sugars). | # Measure OD600 and dilute to OD600=0.25A in 15mL of LB-Chlor with added arabinose (or other sugars). |
Revision as of 01:31, 22 October 2009
All characterization of BBa_K206000 was done using BW27783 cells carrying the construct BBa_K206002. Transfer FunctionWe attempted to find the transfer function relating input concentration of arabinose to PoPS by measuring RFP production in response to varying arabinose concentration. We fit a Hill equation to the data from our experiment and used it to determine the values listed in our datasheet.
Expression RateWe measured the development of RFP over time, in response to intermediate concentrations of arabinose. SpecificityWe investigated the specificity of BBa_K206000 for its ligand, arabinose, by testing it against several other aldopentoses (except rhamnose, a methyl-pentose). Summary Datasheet
1Measured by the UBC iGEM Team 2009 General Characterization Protocols
Sugars were made up to 10% w/v or 500uM stock solutions in water and filter sterilized with a 0.45um filter. RFP fluorescence was measured by pelleting 500uL of cells and resuspending in PBS, then collecting 50000 events on a Becton-Dickinson Influx flow cytometer. Fluorescence was calculated by finding the mean of the RFP histogram for each sample, normalized to OD600 (when possible). |