Fluorescence lifetime snapshots reveal two rapidly reversible mechanisms of photoprotection in live cells of Chlamydomonas reinhardtii

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 109; no. 22; pp. 8405 - 8410
• Main Authors: Amarnath, Kapil, Zaks, Julia, Park, Samuel D, Niyogi, Krishna K, Fleming, Graham R
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 29-05-2012; National Acad Sciences
• Subjects: Algae; Algorithms; autotrophs; Biological Sciences; Cells; Chlamydomonas reinhardtii; Chlamydomonas reinhardtii - metabolism; Chlamydomonas reinhardtii - radiation effects; Chlorophyll; Chlorophyll - chemistry; Chlorophyll - metabolism; Chlorophylls; Energy Transfer - radiation effects; Fluorescence; Lasers; Light; light intensity; Light-Harvesting Protein Complexes - metabolism; Models, Biological; Photochemistry - methods; Photons; photostability; Photosynthesis; Photosynthesis - radiation effects; Photosystem II; Photosystem II Protein Complex - metabolism; Physical Sciences; Plants; Shutters; Thylakoids; Time Factors
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1205303109

Photosynthetic organisms avoid photodamage to photosystem II (PSII) in variable light conditions via a suite of photoprotective mechanisms called nonphotochemical quenching (NPQ), in which excess absorbed light is dissipated harmlessly. To quantify the contributions of different quenching mechanisms to NPQ, we have devised a technique to measure the changes in chlorophyll fluorescence lifetime as photosynthetic organisms adapt to varying light conditions. We applied this technique to measure the fluorescence lifetimes responsible for the predominant, rapidly reversible component of NPQ, qE, in living cells of Chlamydomonas reinhardtii. Application of high light to dark-adapted cells of C. reinhardtii led to an increase in the amplitudes of 65 ps and 305 ps chlorophyll fluorescence lifetime components that was reversed after the high light was turned off. Removal of the pH gradient across the thylakoid membrane linked the changes in the amplitudes of the two components to qE quenching. The rise times of the amplitudes of the two components were significantly different, suggesting that the changes are due to two different qE mechanisms. We tentatively suggest that the changes in the 65 ps component are due to charge-transfer quenching in the minor light-harvesting complexes and that the changes in the 305 ps component are due to aggregated light-harvesting complex II trimers that have detached from PSII. We anticipate that this technique will be useful for resolving the various mechanisms of NPQ and for quantifying the timescales associated with these mechanisms.