Handbook of Plant and Crop Physiology

(Steven Felgate) #1

  1. B El Hamouri, C Sironval. A new non-photoreducible protochlorophyll(ide)-protein P649-642: NADPH me-
    diation of its transformation to photoreducible P657-650. FEBS Lett 103:343–347, 1979.

  2. B Schoefs. Photoreduction of Protochlorophyllide ato Chlorophyllide aDuring the Biogenesis of the Photo-
    synthetic Apparatus in Higher Plants. Ann Arbor, MI: Bell & Howell, 2000.

  3. B El Hamouri, M Brouers, C Sironval. Pathway from photoinactive P633-628 protochlorophyllide to the P696-
    682 chlorophyllide in cucumber etioplast suspension. Plant Sci Lett 21:375–379, 1981.

  4. B Schoefs, F Franck, M Bertrand. Spectroscopic properties of regenerated photoactive protochlorophyllide af-
    ter a flash at two different leaf developmental stages. In: JC Merlin, S Turrell, JP Huvenne, eds. Proceedings
    of the 6th International Conference on the Spectroscopy of Biological Molecules, Dordrecht: Kluwer Aca-
    demic Publishers, 1995, pp 611–612.

  5. DJ McCormac, CA Marwood, D Bruce, BM Greenberg. Assembly of photosystem I and II during the early
    phase of light-induced development of chloroplasts from proplastids in Spirodela oligorrhiza. Photochem Pho-
    tobiol 63:837–845, 1996.

  6. B Schoefs, H-P Garnir, M Bertrand. Comparison of the photoreduction of protochlorophyllide to chlorophyl-
    lide in leaves and cotyledons from dark grown bean as a function of age. Photosynth Res 41:405–417, 1994.

  7. E Selstam, A Widell, LB Johansson. A comparison of prolamellar bodies from wheat, Scots pine and Jeffrey
    pine. Pigment spectra and properties of protochlorophyllide oxidoreductase. Physiol Plant 70:209–214, 1987.

  8. A Lindsten, M Ryberg, C Sundqvist. The polypeptide composition of highly purified prolamellar bodies and
    prothylakoids from wheat (Triticum aestivum) as revealed by silver staining. Physiol Plant 72:167–176, 1988.

  9. C Sironval, Y Kuyper, J-M Michel, M Brouers. On the primary photoact in the conversion of protochloro-
    phyllide into chlorophyllide. Studia Biophys 5:43–50, 1967.

  10. TW Griffiths. Protochlorophyllide photoreduction. In: H Scheer, ed. Chlorophylls. Boca Raton, FL: CRC
    Press, 1991, pp 433–450.

  11. C Sironval. The protochlorophyllide-chlorophyllide cycle as a source of photosynthetically active chloro-
    phylls. In: G Akoyunoglou, ed. Photosynthesis. Vol 5: Chloroplast Development. Philadelphia: Balaban Inetr-
    national Science Service, 1981, pp 3–14.

  12. M Jouy, C Sironval. Quenching of the fluorescence emitted by P695-684 at room temperature in etiolated il-
    luminated leaves. Planta 147:123–133, 1979.

  13. S Bauer, W Siegelman. Photoconversion of chlorophyllide 684 to chlorophyllide 678. FEBS Lett 20:352–354,
    1972.

  14. F Franck, Y Inoue. Light-driven reversible transformation of chlorophyllide P696-684 into chlorophyllide
    P688-676 in illuminated etiolated leaves. Photobiochem Photobiophys 8:85–96, 1984.

  15. F Franck, GH Schmid. On the correlation between oxygen uptake in plastids of greening etiolated oat leaves
    and pigment photooxidation. Z Naturforsch 40c:699–704, 1985.

  16. B Schoefs, F Franck. Role of NADPH-protochlorophyllide-reductase in photoprotection of newly formed
    chlorophyllide (Chlide). In: P Mathis, ed. Photosynthesis: from Light to Biosphere. Vol 3. Dordrecht: Kluwer
    Academic Publishers, 1995, pp 1009–1012.

  17. F Franck, B Schoefs, X Barthélemy, B Mysliwa-Kurdziel, K Strzalka, R Popovic. Protection of native chloro-
    phyll(ide) forms of photosystem II against photodamage during early stages of chloroplast differentiation. Acta
    Physiol Plant 17:123–132, 1995.

  18. TE Redlinger, MC McDaniel. Light-mediated oxygen uptake measured in wheat etioplast. Plant Physiol
    60:452–456, 1977.

  19. C Lütz. Distribution of carotenoids and lipids in separated prolamellar bodies and prothylakoids of etioplasts
    fromAvena sativaL. Z Pflanzenphysiol 104S:43–52, 1981.

  20. WL Butler. Chloroplast development: energy transfer and structure. Arch Biochem Biophys 92:287–299,
    1961.

  21. M Bertrand, B Schoefs. Photosynthetic pigment metabolism in plants during stress. In: M Pessarakli, ed. Hand-
    book of Plant and Crop Stress. 2nd ed. New York: Marcel Dekker, 1999, pp 527–543.

  22. U Sperling, B van Cleve, G Frick, K Apel, G Armstrong. Overexpression of light-dependent PORA and PORB
    in plants depleted of endogenous POR by far-red light enhances seedlings survival in white-light and protects
    against photooxidative damage. Plant J 12:649–658, 1997.

  23. F Franck, B Bereza, B Böddi. Protochlorophyllide-NADPand protochlorophyllide-NADPH complexes and
    their regeneration after flash illumination in leaves and etioplast membranes of dark-grown wheat. Photosynth
    Res 59:53–61, 1999.

  24. S Süzer, K Sauer. The site of photoconversion of protochlorophyllide to chlorophyllide in barley seedlings.
    Plant Physiol 48:60–64, 1971.

  25. JK Hoober, WJ Stegemann. Control of the synthesis of a major polypeptide of chloroplast membranes in
    Chlamydomonas reinhardtii. J Cell Biol 56:1–12, 1973.

  26. RG Alscher, SP Hawkes, K Sauer. The association of protein synthesis with protochlorophyllide holochrome
    regeneration in dark-grown barley leaves. Biochem Biophys Res Commun 73:240–247, 1976.

  27. J Catsky, Z Sestak. Photosynthesis during leaf ageing. In: M Pessarakli, ed. Handbook of Photosynthesis. New
    York: Marcel Dekker, 1997, pp 633–661.

  28. AA Shlyk, GY Savchenko, VG Averina. Investigation of the kinetics of photoreduction of protochlorophyllide
    in green leaves by the spectrofluorographic method. Biofizika 14:119–129, 1969.


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