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. 1979 Feb;63(2):375–381. doi: 10.1104/pp.63.2.375

Ultrastructural Comparison of Cyanidium caldarium Wild Type and III-C Mutant Lacking Phycobilisomes

Francis-André Wollman 1
PMCID: PMC542832  PMID: 16660731

Abstract

Cyanidium caldarium wild type and III-C mutant lacking phycobilisomes were compared with respect to the ultrastructural organization of particles on the freeze-fractured thylakoid membrane.

In the wild type, the particles on the exoplasmic fracture face were arranged in the same manner as that reported for the phycobilisomes on the membrane surface. The phycobilisomes constitute the major part of the photosystem II antenna and their absence in the III-C mutant was accompanied by a completely different arrangement of the particles on the exoplasmic fracture face.

The density of these particles was almost two times higher in the mutant than in the wild type while that of the particles on the protoplasmic fracture face was about the same.

The relative densities of the particles on the exoplasmic fracture face in the two organisms was consistent with the 2-fold higher photosystem II to photosystem I ratio in the mutant compared to the wild type as determined by measurements of the field indicating absorbance changes.

These particles were 100 Angstroms in both organisms.

It is concluded that the particles on the exoplasmic fracture face in Cyanidium are probably substructural units of the particles observed on the same surface in higher plants and green algae and attributed to photosystem II.

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Selected References

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  1. Armond P. A., Staehelin L. A., Arntzen C. J. Spatial relationship of photosystem I, photosystem II, and the light-harvesting complex in chloroplast membranes. J Cell Biol. 1977 May;73(2):400–418. doi: 10.1083/jcb.73.2.400. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benedetti E. L., Dunia I., Bentzel C. J., Vermorken A. J., Kibbelaar M., Bloemendal H. A portrait of plasma membrane specializations in eye lens epithelium and fibers. Biochim Biophys Acta. 1976 Dec 14;457(3-4):353–384. doi: 10.1016/0304-4157(76)90004-6. [DOI] [PubMed] [Google Scholar]
  3. Bennoun P. Réoxydation du quencher de fluorescence "Q" en présence de 3-(3,4-dichlorophényl)-1,1-diméthylurée. Biochim Biophys Acta. 1970 Sep 1;216(2):357–363. doi: 10.1016/0005-2728(70)90227-6. [DOI] [PubMed] [Google Scholar]
  4. Diner B. A. Energy Transfer from the Phycobilisomes to Photosystem II Reaction Centers in Wild Type Cyanidium caldarium. Plant Physiol. 1979 Jan;63(1):30–34. doi: 10.1104/pp.63.1.30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. Edwards M. R., Gantt E. Phycobilisomes of the thermophilic blue-green alga Synechococcus lividus. J Cell Biol. 1971 Sep;50(3):896–900. doi: 10.1083/jcb.50.3.896. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Elgsaeter A., Branton D. Intramembrane particle aggregation in erythrocyte ghosts. I. The effects of protein removal. J Cell Biol. 1974 Dec;63(3):1018–1036. doi: 10.1083/jcb.63.3.1018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gantt E., Conti S. F. Granules associated with the chloroplast lamellae of Porphyridium cruentum. J Cell Biol. 1966 Jun;29(3):423–434. doi: 10.1083/jcb.29.3.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Goodenough U. W., Staehelin L. A. Structural differentiation of stacked and unstacked chloroplast membranes. Freeze-etch electron microscopy of wild-type and mutant strains of Chlamydomonas. J Cell Biol. 1971 Mar;48(3):594–619. doi: 10.1083/jcb.48.3.594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. 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]
  11. Joliot P., Delosme R. Flash-induced 519 nm absorption change in green algae. Biochim Biophys Acta. 1974 Aug 23;357(2):267–284. doi: 10.1016/0005-2728(74)90066-8. [DOI] [PubMed] [Google Scholar]
  12. Junge W., Witt H. T. On the ion transport system of photosynthesis--investigations on a molecular level. Z Naturforsch B. 1968 Feb;23(2):244–254. doi: 10.1515/znb-1968-0222. [DOI] [PubMed] [Google Scholar]
  13. Ley A. C., Butler W. L. Efficiency of energy transfer from photosystem II to photosystem I in Porphyridium cruentum. Proc Natl Acad Sci U S A. 1976 Nov;73(11):3957–3960. doi: 10.1073/pnas.73.11.3957. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Miller K. R. A particle spanning the photosynthetic membrane. J Ultrastruct Res. 1976 Jan;54(1):159–167. doi: 10.1016/s0022-5320(76)80018-4. [DOI] [PubMed] [Google Scholar]
  15. Miller K. R., Staehelin L. A. Analysis of the thylakoid outer surface. Coupling factor is limited to unstacked membrane regions. J Cell Biol. 1976 Jan;68(1):30–47. doi: 10.1083/jcb.68.1.30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. 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]
  17. Ojakian G. K., Satir P. Particle movements in chloroplast membranes: quantitative measurements of membrane fluidity by the freeze-fracture technique. Proc Natl Acad Sci U S A. 1974 May;71(5):2052–2056. doi: 10.1073/pnas.71.5.2052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Ophir I., Ben-Shaul Y. Structural organization of developing chloroplasts in Euglena. Protoplasma. 1974;80(1):109–127. doi: 10.1007/BF01666354. [DOI] [PubMed] [Google Scholar]
  19. Park R. B., Pfeifhofer A. O. Ultrastructural observations on deep-etched thylakoids. J Cell Sci. 1969 Jul;5(1):299–311. doi: 10.1242/jcs.5.1.299. [DOI] [PubMed] [Google Scholar]
  20. Rntzen C. J., Dilley R. A., Crane F. L. A comparison of chloroplast membrane surfaces visualized by freeze-etch and negative staining techniques; and ultrastructural characterization of membrane fractions obtained from digitonin-treated spinach chloroplasts. J Cell Biol. 1969 Oct;43(1):16–31. doi: 10.1083/jcb.43.1.16. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Seckbach J. On the fine structure of the acidophilic hot-spring alga Cyanidium caldarium: a taxonomic approach. Microbios. 1972 Mar-Apr;5(18):133–142. [PubMed] [Google Scholar]
  22. Staehelin L. A. Chloroplast membrane structure. Intramembranous particles of different sizes make contact in stacked membrane regions. Biochim Biophys Acta. 1975 Oct 10;408(1):1–11. doi: 10.1016/0005-2728(75)90153-x. [DOI] [PubMed] [Google Scholar]

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