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200ml of dense culture was concentrated by centrifuging 25,000 x g for 15 minutes. The subsequent cell pellet was resuspended in 5ml of sterile growth media. Cell concentrate was dark acclimated for 10 minutes and 200ul was used to measure the fluorescence spectra. After each measurement, the temperature increased and cells were dark acclimated at that temperature for an additional 10 minutes. This continued until the fluorescence decreased to ~0 indicating the disassociation of the photosynthetic apparatus. This was done following the methods published in Pittera et al., 2017.

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