Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1977 Jan;17(1):1–15. doi: 10.1016/S0006-3495(77)85623-3

Exciton Annihilation in the Two Photosystems in Chloroplasts at 100°K

Nicholas E Geacintov, Jacques Breton
PMCID: PMC1473232  PMID: 831854

Abstract

The fluorescence yield (F) of spinach chloroplasts at 100°K measured at 735 nm (photosystem I fluorescence—F 735) and at 685 nm (photosystem II fluorescence—F 685) has been determined with different modes of laser excitation. The modes of excitation included a single picosecond pulse, sequences of picosecond pulses (4, 22, and 300 pulses spaced 5 ns apart) and a single nonmode-locked 2-μs pulse (MP mode). The F 735/F 685 intensity ratios decrease from 1.62 to 0.61 when a single picosecond pulse (or low-power continuous helium-neon laser) is replaced by excitation with the 300-ps pulse train (PPT mode) or MP mode. In the PPT mode of excitation, the 735-nm fluorescence band is quenched by a factor of 45 as the intensity is increased from 1015 to 1018 photons/cm2 per pulse train and the 685-nm fluorescence is quenched by a factor of 10. In the MP mode, the quenching factors are 25 and 7, respectively, in the same intensity range. Fluorescence quantum yield measurements with different picosecond pulse sequences indicate that relatively long-lived quenching species are operative, which survive from one picosecond pulse to another within the pulse train. The excitonic processes possible in the photosynthetic units are discussed in detail. The differences in the quenching factors between the MP and PPT modes of excitation are attributed to singlet-singlet annihilation, possible when picosecond pulses are utilized, but minimized in the MP mode of excitation. The long-lived quenchers are identified as triplets and/or bulk chlorophyll ions formed by singlet-singlet annihilation. The preferential quenching in photosystem I is attributed to triplet excitons. The influence of heating effects, photochemistry, bleaching, and two-photon processes is also considered and is shown to be negligible.

Full text

PDF
1

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Butler W. L. On the primary nature of fluorescence yield changes associated with photosynthesis. Proc Natl Acad Sci U S A. 1972 Nov;69(11):3420–3422. doi: 10.1073/pnas.69.11.3420. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Campillo A. J., Kollman V. H., Shapiro S. L. Intensity Dependence of the Fluorescence Lifetime of in vivo Chlorophyll Excited by a Picosecond Light Pulse. Science. 1976 Jul 16;193(4249):227–229. doi: 10.1126/science.193.4249.227. [DOI] [PubMed] [Google Scholar]
  3. Campillo A. J., Shapiro S. L., Kollman V. H., Winn K. R., Hyer R. C. Picosecond exciton annihilation in photosynthetic systems. Biophys J. 1976 Jan;16(1):93–97. doi: 10.1016/S0006-3495(76)85666-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cho F., Govindjee Fluorescence spectra of Chlorella in the 295-77 degree K range. Biochim Biophys Acta. 1970 Jun 30;205(3):371–378. doi: 10.1016/0005-2728(70)90103-9. [DOI] [PubMed] [Google Scholar]
  5. Goedheer J. C., Verhülsdonk C. A. Fluorescence and phototransformation of protochlorophyll with etiolated bean leaves from minus 196 to +20 degrees C. Biochem Biophys Res Commun. 1970 Apr 24;39(2):260–266. doi: 10.1016/0006-291x(70)90787-4. [DOI] [PubMed] [Google Scholar]
  6. Joliot P., Bennoun P., Joliot A. New evidence supporting energy transfer between photosynthetic units. Biochim Biophys Acta. 1973 May 30;305(2):317–328. doi: 10.1016/0005-2728(73)90179-5. [DOI] [PubMed] [Google Scholar]
  7. Kitajima M., Butler W. L. Excitation spectra for photosystem I and photosystem II in chloroplasts and the spectral characteristics of the distributions of quanta between the two photosystems. Biochim Biophys Acta. 1975 Dec 11;408(3):297–305. doi: 10.1016/0005-2728(75)90131-0. [DOI] [PubMed] [Google Scholar]
  8. Mathis P., Vermeglio A. Chlorophyll radical cation in photosystem II of chloroplasts. Millisecond decay at low temperature. Biochim Biophys Acta. 1975 Sep 8;396(3):371–381. doi: 10.1016/0005-2728(75)90143-7. [DOI] [PubMed] [Google Scholar]
  9. Mauzerall D. Light-induced fluorescence changes in Chlorella, and the primary photoreactions for the production of oxygen. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1358–1362. doi: 10.1073/pnas.69.6.1358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Mauzerall D. Multiple excitations in photosynthetic systems. Biophys J. 1976 Jan;16(1):87–91. doi: 10.1016/S0006-3495(76)85665-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Shuvalov V. A. The study of the primary photoprocesses in photosystem I of chloroplasts. Recombination luminescence, chlorophyll triplet state and triplet-triplet annihilation. Biochim Biophys Acta. 1976 Apr 9;430(1):113–121. doi: 10.1016/0005-2728(76)90227-9. [DOI] [PubMed] [Google Scholar]
  12. Swenberg C. E., Geacintov N. E., Pope M. Bimolecular quenching of excitons and fluorescence in the photosynthetic unit. Biophys J. 1976 Dec;16(12):1447–1452. doi: 10.1016/S0006-3495(76)85786-4. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES