Team:Cambridge-JIC/Guide/Transformation/Cocultivation

From 2014.igem.org

Revision as of 01:17, 16 October 2014 by Salil (Talk | contribs)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

The time window for commencing cocultivation is when spores are 5-7 days old. Sterilise spores and plate them on 1/2 B5 1.2% agar plates. Leave them to germinate under full illumination. Using an average of 0.5-1 sporehead's worth of spores gives a good quantity of transformants.

1. Make 10-15ml liquid cultures (LB) of agrobacteria from the transformation plates, and leave for 18 hours to grow. It is recommended to use fresh plates for this step to ensure that the agro is nice and virulent. 2. When LB is saturated, spin cultures down at 3000g for 10 minutes. 3. Resuspend the pellet in 2ml 1/2 GB + 100uM acetosyringone 4. Leave the resuspended culture shaking (120rpm is sufficient) at room temperature for 6 hours. Overnight is OK, but 6 hours is optimal. 5. Scrape spores into sterile conical flasks (autoclave them first) containing 25ml 1/2 B5 + 100uM acetosyringone 6. Add 1ml of the agrobacterium mixture that has been shaking for 6 hours. 7. Shake flasks (120rpm is sufficient) under full illumination for between 36-72 hours. 8. Using a 40um sterile filter, wash the spores with 150ml of sterile water with 100ug/ml cefotaxime. 9. Plate spores on selective plates.

For a detailed reference on this protocol and a comparison of the optimal durations of each step, see ...