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• Culture transfer:

Under a laminar flow hood, a sterile flask is filled with the appropriate culture medium.
Approximately 1 ml of initial culture is then transferred into into the new flask using a sterile Pasteur pipette.

• Development phase:

The cultures are placed in a growth room at 20°C, with 16h/8h alternating light/dark for about 2 weeks.

• Conservation phase:

Once the culture has produced enough biomass, it is transferred to a growth room at 7°C, with 12h/12h alternating light/dark.