Transient etiolation: Protochlorophyll(ide) and chlorophyll forms in differentiating plastids of closed and breaking leaf buds of horse chestnut (Aesculus hippocastanum)

Tree Physiology

Volumn 26, Issue 8, 2006, Pages 1087-1096

  Solymosi, Katalin ^a   Bóka, Károly ^a   Böddi, Béla ^a  

^a EÖTVÖS LORÁND UNIVERSITY   (Hungary)

Author keywords

Bud scale; Etio chloroplast; Leaf primordia; LPOR; NADPH:protochlorophyllide oxidoreductase; Prolamellar body; Proplastid; Prothylakoids

Indexed keywords

BUD; CHLOROPHYLL; GERMINATION; LEAF; PIGMENT; PLASTID; TREE;

AESCULUS; AESCULUS HIPPOCASTANUM;

EID: 33747834093     PISSN: 0829318X     EISSN: None     Source Type: Journal    
DOI: 10.1093/treephys/26.8.1087     Document Type: Article

References (49)

1. Amirjani, R. and C. Sundqvist. 2004. Regeneration of protochlorophyllide in green and greening leaves of plants with varying proportions of protochlorophyllide forms in darkness. Physiol. Plant. 121:377-390.
2. Böddi, B., M. Ryberg and C. Sundqvist. 1992. Identification of four universal protochlorophyllide forms in dark-grown leaves by analyses of the 77 K fluorescence emission spectra. J. Photochem. Photobiol. B: Biol. 12:389-401.
3. Böddi, B., B. McEwen, M. Ryberg and C. Sundqvist. 1994. Protochlorophyllide forms in non-greening epicotyls of dark-grown pea (Pisum sativum). Physiol. Plant. 92:706-713.
4. Böddi, B., K. Kis-Petik, A.D. Kaposi, J. Fidy and C. Sundqvist. 1998. The two spectroscopically different short wavelength protochlorophyllide forms in pea epicotyls are both monomeric. Biochim. Biophys. Acta 1365:531-540.
5. Böddi, B., A. Lindsten and C. Sundqvist. 1999. Chlorophylls in dark-grown epicotyl and stipula of pea. J. Photochem. Photobiol. B: Biol. 48:11-16.
6. Bradbeer, J.W., A.O. Gyldenholm, J.W. Smith, J. Rest and H.J.W. Edge. 1974. Plastid development in primary leaves of Phaseolus vulgaris IX. The effects of short light treatments on plastid development. New Phytol. 73:281-290.
7. Casadoro, G. and N. Rascio. 1987. Cotyledonal chloroplasts in the hypogeal seeds of clementine. Planta 170:300-307.
8. Chatfield, S.P., P. Stirnberg, B.G. Forde and O. Leyser. 2000. The hormonal regulation of axillary bud growth in Arabidopsis. Plant J. 24:159-69.
9. Franck, F. and K. Strzałka. 1992. Detection of the photoactive protochlorophyllide-protein complex in the light during the greening of barley. FEBS Lett. 309:73-77.
10. Franck, F., X. Barthélémy and K. Strzałka. 1993. Spectroscopic characterization of protochlorophyllide photoreduction in the greening leaf. Photosynthetica 29:185-194.
11. Girnth, C., R. Bergfeld and H. Kasemir. 1978. Phytochrome-mediated control of grana and stroma thylakoid formation in plastids of mustard cotyledons. Planta 141:191-198.
12. Gunning, B.E.S. 1965. The greening process in plastids. 1. The structure of the prolamellar body. Protoplasma 60:111-130.
13. Gunning, B.E.S. 2001. Membrane geometry of "open" prolamellar bodies. Protoplasma 215:4-15.
14. He, Z.-H., J. Li, C. Sundqvist and M.P. Timko. 1994. Leaf developmental age controls expression of genes encoding enzymes of chlorophyll and heme biosynthesis in pea (Pisum sativum). Plant. Physiol. 106:537-546.
15. Henningsen, K.W. and J.E. Boynton. 1969. Macromolecular physiology of plastids, VII. The effect of brief illumination on plastids of dark-grown barley leaves. J. Cell Sci. 5:757-793.
16. Kis-Petik, K., B. Böddi, A.D. Kaposi and J. Fidy. 1999. Protochlorophyllide forms and energy transfer in dark-grown wheat leaves. Studies by conventional and laser excited fluorescence spectroscopy between 10 K-100 K. Photosynth. Res. 60:87-98.
17. Klein, S. and J.K. Schiff. 1972. The correlated appearance of prolamellar bodies, protochlorophyllide species, and the Shibata shift during development of bean etioplasts in the dark. Plant Physiol. 49:619-626.
18. Kuroda, H., T. Masuda, H. Ohta, Y. Shioi and K. Takamiya. 1996. Effects of light, developmental age and phytohormones on the expression of the gene encoding NADPH-protochlorophyllide oxidoreductase in Cucumis sativus. Plant Physiol. Biochem. 34: 17-22.
19. Laetsch, W.M. and I. Price. 1969. Development of the dimorphic chloroplasts of sugar cane. Am. J. Bot. 56:77-87.
20. Marinos, N.G. 1967. Multifunctional plastids in the meristematic region of potato tuber buds. J. Ultrastr. Res. 17:91-113.
21. Masuda, T. and K. Takamiya. 2004. Novel insights into the enzymology, regulation and physiological functions of light-dependent protochlorophyllide oxidoreductase in angiosperms. Photosynth. Res. 81:1-29.
22. McEwen, B., H.I. Virgin, B. Böddi and C. Sundqvist. 1991. Protochlorophyll forms in roots of dark-grown plants. Physiol. Plant. 81:455-461.
23. McEwen, B., C. Sundqvist and S. Younis. 1994. Protochlorophyll(ide) forms in hypocotyls of dark-grown bean (Phaseolus vulgaris). Physiol. Plant. 90:396-407.
24. Minkov, I.N., M. Ryberg and C. Sundqvist. 1988. Properties of reformed prolamellar bodies from illuminated and redarkened etiolated wheat plants. Physiol. Plant. 72:725-732.
25. Rascio, N., M. Orsenigo and D. Arboit. 1976. Prolamellar body transformation with increasing cell age in the maize leaf. Protoplasma 90:253-263.
26. Rascio, N., P. Mariani Colombo and M. Orsenigo. 1980. The ultrastructural development of plastids in leaves of maize plants exposed to continuous illumination. Protoplasma 102:131-139.
27. Rascio, N., P. Mariani and G. Casadoro. 1984. Etioplast-chloroplast transformation in maize leaves: effects of tissue age and light intensity. Protoplasma 119:110-120.
28. Rascio, N., P. Mariani, P. Chitano and F. Dalla Vecchia. 1986. An ultrastructural study of maize leaf etioplasts throughout their entire life-cycle. Protoplasma 130:98-107.
29. Reynolds, E.S. 1963. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J. Cell. Biol. 17: 208-212.
30. Robertson, D. and W.M. Laetsch. 1974. Structure and function of developing barley plastids. Plant Physiol. 54:148-159.
31. Ryberg, M. and C. Sundqvist. 1991. Structural and functional significance of pigment protein complexes of chlorophyll precursors. In Chlorophylls. Ed. H. Sheer. CRC Press Inc., Boca Raton, Florida, pp 587-612.
32. Schoefs, B. 2001. The protochlorophyllide-chlorophyllide cycle. Photosynth. Res. 70:257-271.
33. Schoefs, B. and F. Franck. 1993. Photoreduction of protochlorophyllide to chlorophyllide in 2-d-old dark-grown bean (Phaseolus vulgaris cv. Commodore) leaves. Comparison with 10-d-old dark-grown (etiolated) leaves. J. Exp. Bot. 44: 1053-1057.
34. Schoefs, B., M. Bertrand and F. Franck. 2000a. Spectroscopic properties of protochlorophyllide analyzed in situ in the course of etiolation and in illuminated leaves. Photochem. Photobiol. 72:85-93.
35. Schoefs, B., M. Bertrand and C. Funk. 2000b. Photoactive protochlorophyllide regeneration in cotyledons and leaves from higher plants. Photochem. Photobiol. 72:660-668.
36. Seyedi, M., E. Selstam, M.P. Timko and C. Sundqvist. 2001. The cytokinin 2-isopentenyladenine causes partial reversion to skotomorphogenesis and induces formation of prolamellar bodies and protochlorophyllide657 in the lip1 mutant of pea. Physiol. Plant. 112:261-272.
37. Skribanek, A. and B. Böddi. 2001. Light- and cold-stress effects on the greening process in epicotyls and young stems of red oak (Quercus rubra) seedlings. Tree Physiol. 21:549-554.
38. Skribanek, A., D. Apatini, M. Inaoka and B. Böddi. 2000. Protochlorophyllide and chlorophyll forms in dark-grown stems and stem-related organs. J. Photochem. Photobiol. B: Biol. 55: 172-177.
39. Solymosi, K. and B. Böddi. 2006. Optical properties of bud scales and protochlorophyll(ide) forms in leaf primordia of closed and opened buds. Tree Physiol. 26:1071-1081.
40. Solymosi, K., K. Martinez, Z. Kristóf, C. Sundqvist and B. Böddi. 2004. Plastid differentiation and chlorophyll biosynthesis in different leaf layers of white cabbage (Brassica oleracea cv. capitata). Physiol. Plant. 121:520-529.
41. Sperling, U., B. van Cleve, G. Frick, K. Apel and G.A. Armstrong. 1997. Overexpression of light-dependent PORA or PORB in plants depleted of endogenous POR by far-red light enhances seedling survival in white light and protects against photooxidative damage. Plant J. 12:649-658.
42. Sperling, U., F. Franck, B. van Cleve, G. Frick, K. Apel and G.A. Armstrong. 1998. Etioplast differentation in Arabidopsis: both PORA and PORB restore the prolamellar body and photoactive protochlorophyllide-F655 to the cop1 photomorphogenic mutant. Plant Cell 10:283-296.
43. Sundqvist, C. and C. Dahlin. 1997. With chlorophyll pigments from prolamellar bodies to light-harvesting complexes. Physiol. Plant. 100:748-759.
44. Treffry, T. 1973. Chloroplast development in etiolated peas: reformation of prolamellar bodies in red light without accumulation of protochlorophyllide. J. Exp. Bot. 24:185-195.
45. Weier, T.E., R.D. Sjoland and D.L. Brown. 1970. Changes induced by low light intensities on the prolamellar body of 8-day, dark-grown seedlings. Am. J. Bot. 57:276-284.
46. Wellburn, A.R., D.C. Robinson and F.A.M. Wellburn. 1982. Chloroplast development in low-light grown barley seedlings. Planta 154:259-265.
47. Whatley, J.M. 1977. Variations in the basic pathway of chloroplast development. New Phytol. 78:407-420.
48. Wrischer, M. 1966. Neubildung von Prolamellarkörpern in Chloroplasten. Z. Pflanzenphysiol. 55:296-299.
49. Wrischer, M. 1973. Ultrastructural changes in isolated plastids. II. Etio-chloroplasts. Protoplasma 78:417-425.