Team:Osaka/Protocols

Protocols

Cell survival assay 1: UV irradiation

1. Pre-culture transformed cells in 3ml of LB medium at 37°C for 16h.
2. Induce parts with IPTG addition (to final concentration of 100µM) for 1h.
3. Dilute pre-culture samples according to intended UV energy dosage (if dosage is high, lower dilution rate is needed as fewer cells are expected to survive).
4. Transfer 50μl of diluted pre-culture onto LB agar plates and spread evenly. Air-dry the plates to remove excess wetness.
5. Irradiate cells on the agar with UV light at desired energy dosage.
6. Wrap plates in aluminium foil and incubate at 37°C.
7. After 16h, count number of colonies formed on control (non-irradiated) and UV-irradiated plates.

Cell survival assay 2: Mitomycin C

1. Pre-culture transformed cells in 3ml of LB medium at 37°C for 16h.
2. Induce parts with IPTG addition (to final concentration of 100µM) for 1h.
3. Dilute pre-culture samples according to intended UV energy dosage (if dosage is high, lower dilution rate is needed as fewer cells are expected to survive).
4. Transfer 50μl of diluted pre-culture onto LB agar plates and spread evenly. Air-dry the plates to remove excess wetness.
5. Irradiate cells on the agar with UV light at desired energy dosage.
6. Wrap plates in aluminium foil and incubate at 37°C.
7. After 16h, count number of colonies formed on control (non-irradiated) and UV-irradiated plates.

SOS Promoter assay

1. Pre-culture transformed cells in 8ml of LB medium at 37°C for 12h.
2. Transfer pre-culture to OD600 measurement dish (ø50mm).
3. Irradiate with UV light at desired energy dosage.
4. Incubate irradiated cells for a further 2h.
5. Measure OD600 as a measure of cell density.
6. Transfer cells into 15ml Falcon tubes and centrifuge.
7. Discard supernatant, add 1ml water to wash cells.
8. Repeat centrifugation and decantation.
9. Add 500μl acetone and vortex.
10. Incubate at 55°C for 15min.
11. Measure absorbance at 474nm. Use 100% acetone as blanks, and divide absorbances by OD600 measurements.