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. 1967 Dec 1;35(3):553–584. doi: 10.1083/jcb.35.3.553

BIOGENESIS OF CHLOROPLAST MEMBRANES

II. Plastid Differentiation during Greening of a Dark-Grown Algal Mutant (Chlamydomonas reinhardi)

I Ohad 1, P Siekevitz 1, G E Palade 1
PMCID: PMC2107150  PMID: 6064365

Abstract

Dark-grown cells of the y-1 mutant of Chlamydomonas reinhardi contain a partially differentiated plastid lacking the photosynthetic lamellar system. When exposed to the light, a rapid synthesis of photosynthetic membranes occurs accompanied by synthesis of chlorophyll, lipids, and protein and extensive degradation of the starch reserve. The process is continuously dependent on illumination and is completed within 6–8 hr in the absence of cell division. Photosynthetic activity (O2 evolution, Hill reaction, NADP photo-reduction, and cytochrome f photooxidation) parallels the synthesis of pigment and membrane formation. During the greening process, only slight changes occur in the levels of soluble enzymes associated with the photosynthetic process (RuDP-carboxylase, NADP-linked G-3-P dehydrogenase, alkaline FDPase (pH 8)) as compared with the dark control. Also cytochrome f concentration remains almost constant during the greening process. The kinetics of the synthesis of chlorophyll, formation of photosynthetic membranes, and the restoration of photosynthetic activity suggest that the membranes are assembled from their constituents in a single-step process.

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Selected References

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  1. AMES B. N., DUBIN D. T. The role of polyamines in the neutralization of bacteriophage deoxyribonucleic acid. J Biol Chem. 1960 Mar;235:769–775. [PubMed] [Google Scholar]
  2. Arnon D. I. COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS. Plant Physiol. 1949 Jan;24(1):1–15. doi: 10.1104/pp.24.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BRAWERMAN G., POGO A. O., CHARGAFF E. Induced formation of ribonucleic acids and plastid protein in Euglena gracilis under the influence of light. Biochim Biophys Acta. 1962 Mar 5;55:326–334. doi: 10.1016/0006-3002(62)90787-4. [DOI] [PubMed] [Google Scholar]
  4. Ben-Shaul Y., Schiff J. A., Epstein H. T. Studies of Chloroplast Development in Euglena. VII. Fine Structure of the Developing Plastid. Plant Physiol. 1964 Mar;39(2):231–240. doi: 10.1104/pp.39.2.231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brody M., Brody S. S., Levine J. H. Fluorescence changes during chlorophyll formation in Euglena gracilis (and other organisms) and an estimate of lamellar area as a function of age. J Protozool. 1965 Aug;12(3):465–476. doi: 10.1111/j.1550-7408.1965.tb03243.x. [DOI] [PubMed] [Google Scholar]
  6. Butler W. L. Development of photosynthetic system 1 and 2 in a greening leaf. Biochim Biophys Acta. 1965 May 25;102(1):1–8. doi: 10.1016/0926-6585(65)90198-6. [DOI] [PubMed] [Google Scholar]
  7. CARO L. G., VAN TUBERGEN R. P., KOLB J. A. High-resolution autoradiography. I. Methods. J Cell Biol. 1962 Nov;15:173–188. doi: 10.1083/jcb.15.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. CLARK M. F., MATTHEWS R. E., RALPH R. K. RIBOSOMES AND POLYRIBOSOMES IN BRASSICA PEKINENSIS. Biochim Biophys Acta. 1964 Oct 16;91:289–304. doi: 10.1016/0926-6550(64)90253-1. [DOI] [PubMed] [Google Scholar]
  9. Colombo B., Baglioni C. Regulation of haemoglobin synthesis at the polysome level. J Mol Biol. 1966 Mar;16(1):51–66. doi: 10.1016/s0022-2836(66)80262-0. [DOI] [PubMed] [Google Scholar]
  10. EILAM Y., KLEIN S. The effect of light intensity and sucrose feeding on the fine structure in chloroplasts and on the chlorophyll content of etiolated leaves. J Cell Biol. 1962 Aug;14:169–182. doi: 10.1083/jcb.14.2.169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. EISENSTADT J. M., BRAWERMAN G. THE PROTEIN-SYNTHESIZING SYSTEMS FROM THE CYTOPLASM AND THE CHLOROPLASTS OF EUGLENA GRACILIS. J Mol Biol. 1964 Dec;10:392–402. doi: 10.1016/s0022-2836(64)80060-7. [DOI] [PubMed] [Google Scholar]
  12. GIBBS S. P. Chloroplast development in Ochromonas danica. J Cell Biol. 1962 Nov;15:343–361. doi: 10.1083/jcb.15.2.343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. HULANICKA D., ERWIN J., BLOCH K. LIPID METABOLISM OF EUGLENA GRACILIS. J Biol Chem. 1964 Sep;239:2778–2787. [PubMed] [Google Scholar]
  14. Hudock G. A., McLeod G. C., Moravkova-Kiely J., Levine R. P. The Relation of Oxygen Evolution to Chlorophyll and Protein Synthesis in a Mutant Strain of Chlamydomonas reinhardi. Plant Physiol. 1964 Nov;39(6):898–903. doi: 10.1104/pp.39.6.898. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  16. MARINETTI G. V. CHROMATOGRAPHY OF LIPIDS ON COMMERCIAL SILICA GEL LOADED FILTER PAPER. J Lipid Res. 1965 Apr;6:315–317. [PubMed] [Google Scholar]
  17. MEGO J. L., JAGENDORF A. T. Effect of light on growth of Black Valentine bean plastids. Biochim Biophys Acta. 1961 Oct 28;53:237–254. doi: 10.1016/0006-3002(61)90437-1. [DOI] [PubMed] [Google Scholar]
  18. MIYACHI S., KANAI R., MIHARA S., MIYACHI S., AOKI S. METABOLIC ROLES OF INORGANIC POLYPHOSPHATES IN CHLORELLA CELLS. Biochim Biophys Acta. 1964 Dec 9;93:625–634. doi: 10.1016/0304-4165(64)90345-9. [DOI] [PubMed] [Google Scholar]
  19. MUEHLETHALER K., FREY-WYSSLING A. [Development and structure of proplastids]. J Biophys Biochem Cytol. 1959 Dec;6:507–512. [PMC free article] [PubMed] [Google Scholar]
  20. Margulies M. M. Effect of Chloramphenicol on Light Dependent Development of Seedlings of Phaseolus vulgaris var. Black Valentine, With Particular Reference to Development of Photosynthetic Activity. Plant Physiol. 1962 Jul;37(4):473–480. doi: 10.1104/pp.37.4.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Margulies M. M. Effect of Chloramphenicol on Light-Dependent Synthesis of Proteins and Enzymes of Leaves and Chloroplasts of Phaseolus vulgaris. Plant Physiol. 1964 Jul;39(4):579–585. doi: 10.1104/pp.39.4.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Ohad I., Siekevitz P., Palade G. E. Biogenesis of chloroplast membranes. I. Plastid dedifferentiation in a dark-grown algal mutant (Chlamydomonas reinhardi). J Cell Biol. 1967 Dec;35(3):521–552. doi: 10.1083/jcb.35.3.521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. PERINI F., SCHIFF J. A., KAMEN M. D. IRON-CONTAINING PROTEINS IN EUGLENA. II. FUNCTIONAL LOCALIZATION. Biochim Biophys Acta. 1964 Jul 29;88:91–98. doi: 10.1016/0926-6577(64)90156-1. [DOI] [PubMed] [Google Scholar]
  24. ROSENBERG A., PECKER M. LIPID ALTERATIONS IN EUGLENA GRACILIS CELLS DURING LIGHT-INDUCED GREENING. Biochemistry. 1964 Feb;3:254–258. doi: 10.1021/bi00890a019. [DOI] [PubMed] [Google Scholar]
  25. SAGER R., GRANICK S. Nutritional studies with Chlamydomonas reinhardi. Ann N Y Acad Sci. 1953 Oct 14;56(5):831–838. doi: 10.1111/j.1749-6632.1953.tb30261.x. [DOI] [PubMed] [Google Scholar]
  26. Stern A. I., Schiff J. A., Epstein H. T. Studies of Chloroplast Development in Euglena. V. Pigment Biosynthesis, Photosynthetic Oxygen Evolution and Carbon Dioxide Fixation during Chloroplast Development. Plant Physiol. 1964 Mar;39(2):220–226. doi: 10.1104/pp.39.2.220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. WOLFF J. B., PRICE L. The effect of sugars on chlorophyll biosynthesis in higher plants. J Biol Chem. 1960 Jun;235:1603–1608. [PubMed] [Google Scholar]

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