Team:NYMU-Taipei/Experiments/Protocols
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Promoter Testing
These are the protocols we used for promoter testing
General Gene Reporter Assay protocol
This is our general setup for gene reporting assays.
Previous-night Preparation (~10m-60min)
Previous night:
- Culture overnight (~16hrs) at 37C and shaking at 180rpm 2-3ml of single colonies of things to be measured.
Preparation (can be done the previous night too):
- Determine the number of measurement points = number of items x number of replicates
- Prepare that amount of 15ml round-bottom tubes and 1.5uL microcentrifuge tubes.
- Add 2ml of LB + the relevant antibiotics in each round-bottom tube.
Pre-start (~30mins)
Preparation:
- Prewarm the LB+antibioics to the temperature to test at (e.g. 20mins prewarming in the incubator takes it up to 37C).
- Get some ice buckets and pre-cool down the 1xPBS
Culturing (2~3mins)
- Add any relevant chemicals to the prewarmed round-bottom tubes containing 2ml LB.
- Dilute the overnight culture to an OD600 of about 0.0325
- Incubate at the required conditions (usually 37C and 180rpm).
- Repeat for every replicate.
Measurement point retrieval
For each culture tube:
- Take out the relevant culture and put it on ice
- Extract 1.3ml from the culture tube and put it in an 1.5uL microcentrifuge tube
- Centrifuge for 1min at 16.2g (13.2rpm on tabletop centrifuge)
- WASH: Tip out the supernatant and add 650uL of 1xPBS, resuspend, then centrifuge again.
- WASH again.
- Carefully remove and discard all the supernatant, resuspend in 1.3ml of 1xPBS.
- Store at 4C until measuring
Measuring
Requires black plates for measuring fluorescence and transparent plates for measuring OD600. For each measurement point, load 200uL each into 3 black wells and 3 transparent wells (i.e. 3 technical replicates each for fluorescence and OD600). Measure the fluorescence on the black plate with the settings depending on your machine. We use excitation/emission wavelength of 485/525 (100ms per measurement). Measure the OD600 on the transparent plate.
H202 Promoter Gene Reporter Assay
For measuring promoters under different H202 stress concentrations: (e.g.: 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM, 2mM, 2.5mM, 5mM).
- Add the H202 just before adding the bacteria.