Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1979 Jan;63(1):26–29. doi: 10.1104/pp.63.1.26

Biosynthesis of Photosystem II Reaction Centers, Antenna and Plastoquinone Pool in Greening Cells of Cyanidium caldarium Mutant III-C 1

Bruce A Diner a, Francis-André Wollman a
PMCID: PMC542759  PMID: 16660686

Abstract

Dark-grown etiolated cells of Cyanidium caldarium mutant III-C lacking ≥99% of their normal chlorophyll content and inactive for photosynthesis were greened in continuous light. Measurements of oxygen evolution and fluorescence kinetics indicate that during greening: (a) the photosystem II (PSII) antenna containing between 30 and 40 chlorophyll a per center undergoes little change in size from 5% of the centers synthesized per cell to fully active cells; (b) energy transfer between PSII centers appears very early in the greening process; (c) the plastoquinone pool size per PSII center (about 14 equivalents) does not vary during greening and has already attained full size after synthesis of only 13% of the full complement of centers.

The PSII centers, antenna chlorophyll and plastoquinone are integrated into the membrane with constant stoichiometry throughout at least 90% of the greening process. These components are integrated such that in regions of the membrane containing active PSII centers, their density in the membrane hardly changes over the same period. The center-antenna complex and possibly the plastoquinone pool as well are organized into unit structures containing 40 chlorophyll a and 7 plastoquinones, respectively. Energy transfer between centers in PSII appears following aggregation of the center-antenna units.

Full text

PDF
26

Images in this article

Selected References

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

  1. ALLEN M. B. Studies with Cyanidium caldarium, an anomalously pigmented chlorophyte. Arch Mikrobiol. 1959;32(3):270–277. doi: 10.1007/BF00409348. [DOI] [PubMed] [Google Scholar]
  2. Akoyunoglou G. Development of the photosystem II unit in plastids of bean leaves greened in periodic light. Arch Biochem Biophys. 1977 Oct;183(2):571–580. doi: 10.1016/0003-9861(77)90392-7. [DOI] [PubMed] [Google Scholar]
  3. Armond P. A., Arntzen C. J., Briantais J. M., Vernotte C. Differentiation of chloroplast lamellae. Light harvesting efficiency and grana development. Arch Biochem Biophys. 1976 Jul;175(1):54–63. doi: 10.1016/0003-9861(76)90484-7. [DOI] [PubMed] [Google Scholar]
  4. Diner B. A., Wollman F. A. Functional Comparison of the Photosystem II Center-Antenna Complex of a Phycocyanin-less Mutant of Cyanidium caldarium with That of Chlorella pyrenoidosa. Plant Physiol. 1979 Jan;63(1):20–25. doi: 10.1104/pp.63.1.20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dubertret G., Joliot P. Structure and organization of system II photosynthetic units during the greening of a dark-grown Chlorella mutant. Biochim Biophys Acta. 1974 Sep 20;357(3):399–411. doi: 10.1016/0005-2728(74)90030-9. [DOI] [PubMed] [Google Scholar]
  6. Dubertret G., Lefort-Tran M. Functional and structural organization of chlorophyll in the developing photosynthetic membranes of Euglena gracilis Z. II. Formation of system II photosynthetic units during greening under optimal light intensity. Biochim Biophys Acta. 1978 Aug 8;503(2):316–332. doi: 10.1016/0005-2728(78)90191-3. [DOI] [PubMed] [Google Scholar]
  7. Forbush B., Kok B. Reaction between primary and secondary electron acceptors of photosystem II of photosynthesis. Biochim Biophys Acta. 1968 Aug 20;162(2):243–253. doi: 10.1016/0005-2728(68)90106-0. [DOI] [PubMed] [Google Scholar]
  8. Herron H. A., Mauzerall D. The development of photosynthesis in a greening mutant of chlorella and an analysis of the light saturation curve. Plant Physiol. 1972 Jul;50(1):141–148. doi: 10.1104/pp.50.1.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. JOLIOT A., JOLIOT P. ETUDE CIN'ETIQUE DE LA R'EACTION PHOTOCHIMIQUE LIB'ERANT L'OXYG'ENE AU COURS DE LA PHOTOSYNTH'ESE. C R Hebd Seances Acad Sci. 1964 May 4;258:4622–4625. [PubMed] [Google Scholar]
  10. Kok B., Forbush B., McGloin M. Cooperation of charges in photosynthetic O2 evolution-I. A linear four step mechanism. Photochem Photobiol. 1970 Jun;11(6):457–475. doi: 10.1111/j.1751-1097.1970.tb06017.x. [DOI] [PubMed] [Google Scholar]
  11. NICHOLS K. E., BOGORAD L. Studies on phycobilin formation with mutants of Cyanidium caldarium. Nature. 1960 Dec 3;188:870–872. doi: 10.1038/188870b0. [DOI] [PubMed] [Google Scholar]
  12. Siggel U., Renger G., Stiehl H. H., Rumberg B. Evidence for electronic and ionic interaction between electron transport chains in chloroplasts. Biochim Biophys Acta. 1972 Feb 28;256(2):328–335. doi: 10.1016/0005-2728(72)90063-1. [DOI] [PubMed] [Google Scholar]
  13. Stiehl H. H., Witt H. T. Quantitative treatment of the function of plastoquinone in phostosynthesis. Z Naturforsch B. 1969 Dec;24(12):1588–1598. doi: 10.1515/znb-1969-1219. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES