Desiccoplast-etioplast-chloroplast transformation under rehydration of desiccated poikilochlorophyllous Xerophyta humilis leaves in the dark and upon subsequent illumination

Journal of Plant Physiology

Volumn 170, Issue 6, 2013, Pages 583-590

  Solymosi, Katalin ^a   Tuba, Zoltán ^b   Böddi, Béla ^a  

^a EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^b SZENT ISTVÁN UNIVERSITY   (Hungary)

Author keywords

Chlorophyll biosynthesis; Etioplast; Poikilochlorophyllous desiccation tolerant plant; Protochlorophyllide; Rehydration

Indexed keywords

CHLOROPHYLL; PROTOCHLOROPHYLLIDE; WATER;

ANGIOSPERM; ARTICLE; BIOSYNTHESIS; CHLOROPLAST; DESICCATION; LIGHT; METABOLISM; SPECTROFLUOROMETRY; TRANSMISSION ELECTRON MICROSCOPY;

ANGIOSPERMS; CHLOROPHYLL; CHLOROPLASTS; DESICCATION; LIGHT; MICROSCOPY, ELECTRON, TRANSMISSION; PROTOCHLOROPHYLLIDE; SPECTROMETRY, FLUORESCENCE; WATER;

XEROPHYTA HUMILIS;

EID: 84875068106     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2012.11.022     Document Type: Article

References (55)

1. Alpert P. The discovery, scope, and puzzle of desiccation tolerance in plants. Plant Ecol 2000, 151:15-17.
2. Böddi B., Lindsten A., Ryberg M., Sundqvist C. On the aggregational states of protochlorophyllide and its protein complexes in wheat etioplasts. Physiol Plant 1989, 76:135-143.
3. Böddi B., Ryberg M., Sundqvist C. The formation of a short-wavelength chlorophyllide form at partial phototransformation of protochlorophyllide in etioplast inner membranes. Photochem Photobiol 1991, 53:667-673.
4. Böddi B., Ryberg M., Sundqvist C. Identification of four universal protochlorophyllide forms in dark-grown leaves by analyses of the 77K fluorescence emission spectra. J Photochem Photobiol B: Biol 1992, 12:389-401.
5. Böddi B., McEwen B., Ryberg M., Sundqvist C. Protochlorophyllide forms in non-greening epicotyls of dark-grown pea (Pisum sativum). Physiol Plant 1994, 92:160-170.
6. Böddi B., Lindsten A., Sundqvist C. Chlorophylls in dark-grown epicotyl and stipula of pea. J Photochem Photobiol B: Biol 1999, 48:11-16.
7. Bréhélin C., Kessler F., van Wijk K.J. Plastoglobules: versatile lipoprotein particles in plastids. Trends Plant Sci 2007, 12:260-266.
8. Dace H., Sherwin H.W., Illing N., Farrant J.M. Use of metabolic inhibitors to elucidate mechanisms of recovery from desiccation stress in the resurrection plant Xerophyta humilis. Plant Growth Regul 1998, 24:171-177.
9. Dobek A., Dujardin E., Franck F., Sironval C., Breton J., Roux E. The first events of protochlorophyll(ide) photoreduction investigated in etiolated leaves by means of the fluorescence excited by short, 610nm laser flashes at room temperature. Photobiochem Photobiophys 1981, 2:35-44.
10. Farrant J.M. A comparison of mechanisms of desiccation tolerance among three angiosperm resurrection plant species. Plant Ecol 2000, 151:29-39.
11. Farrant J.M., Cooper K., Kruger L.A., Sherwin H.W. The effect of drying rate on the survival of three desiccation-tolerant angiosperm species. Ann Bot 1999, 84:371-379.
12. Farrant J.M., Vander Willigen C., Loffell D.A., Bartsch S., Whittaker A. An investigation into the role of light during desiccation of three angiosperm resurrection plants. Plant Cell Environ 2003, 26:1275-1286.
13. + and protochlorophyllide-NADPH complexes and their regeneration after flash illumination in leaves and etioplast membranes of dark-grown wheat. Photosynth Res 1999, 59:53-61.
14. Gaff D.F. Desiccation tolerant flowering plants in southern Africa. Science 1971, 174:1033-1034.
15. Griffiths W.T. Reconstitution of chlorophyll formation by isolated etioplast membranes. Biochem J 1978, 174:681-692.
16. Griffiths W.T. Substrate-specificity studies on protochlorophyllide reductase in barley (Hordeum vulgare) etioplast membranes. Biochem J 1980, 186:267-278.
17. Gunning B.E.S. The greening process in plastids, 1. The structure of the prolamellar body. Protoplasma 1965, 60:111-130.
18. Hallam N.D., Luff S.E. Fine structural changes in the mesophyll tissue of the leaves of Xerophyta villosa during desiccation. Bot Gaz 1980, 141:173-179.
19. Hambler D.J. A poikilohydrous, poikilochlorophyllous angiosperm from Africa. Nature 1961, 191:1415-1416.
20. Ingle R.A., Collett H., Cooper K., Takashi Y., Farrant J.M., Illing N. Chloroplast biogenesis during rehydration of the resurrection plant Xerophyta humilis: parallels to the etioplast-chloroplast transition. Plant Cell Environ 2008, 31:1813-1824.
21. Klein S., Schiff J.K. The correlated appearance of prolamellar bodies, protochlorophyllide species, and the Shibata shift during development of bean etioplasts in the dark. Plant Physiol 1972, 49:619-626.
22. Moore J.P., Le N.G., Brandt W.F., Driouich A., Farrant J.M. Towards a systems-based understanding of plant desiccation tolerance. Trends Plant Sci 2009, 14:110-117.
23. Oliver M.J., Tuba Z., Mishler B.D. The evolution of vegetative desiccation tolerance in land plants. Plant Ecol 2000, 151:85-100.
24. Ouazzani-Chahdi M.A., Schoefs B., Franck F. Isolation and characterisation of photoactive complexes of NADPH:protochlorophyllide oxidoreductase from wheat. Planta 1998, 206:673-680.
25. Porembski S. Tropical inselbergs: habitat types, adaptive strategies and diversity patterns. Rev Bras Bot 2007, 30:579-586.
26. Proctor M.C.F., Tuba Z. Poikilohydry and homoihydry: antithesis or spectrum of possibilities? Tansley review no. 141. New Phytol 2002, 156:327-349.
27. Rascio N., La Rocca N. Resurrection plants: the puzzle of surviving extreme vegetative desiccation. Crit Rev Plant Sci 2005, 24:209-225.
28. Robertson D., Laetsch W.M. Structure and function of developing barley plastids. Plant Physiol 1974, 54:148-159.
29. Ryberg M., Dehesh K. Localization of NADPH:protochlorophyllide oxidoreductase in dark-grown wheat (Triticum aestivum) by immuno-electron microscopy before and after transformation of the prolamellar bodies. Physiol Plant 1986, 66:616-624.
30. Ryberg M., Sundqvist C. Spectral forms of protochlorophyllide in prolamellar bodies and prothylakoids fractionated from wheat etioplasts. Physiol Plant 1982, 56:133-138.
31. Ryberg M., Sundqvist C. The regular ultrastructure of isolated prolamellar bodies depends on the presence of membrane-bound NADPH-protochlorophyllide oxidoreductase. Physiol Plant 1988, 73:218-226.
32. Schoefs B., Franck F. Protochlorophyllide reduction: mechanisms and evolution. Photochem Photobiol 2003, 78:543-557.
33. Schoefs B., Garnir H.P., Bertrand M. Comparison of the photoreduction of protochlorophyllide to chlorophyllide in leaves and cotyledons from dark-grown bean as a function of age. Photosynth Res 1994, 41:405-417.
34. Schoefs B., Bertrand M., Franck F. Spectroscopic properties of protochlorophyllide analyzed in situ in the course of etiolation and in illuminated leaves. Photochem Photobiol 2000, 72:85-93.
35. Sherwin H.W., Farrant J.M. Protection mechanisms against excess light in the resurrection plants Craterostigma wilmsii and Xerophyta viscosa. Plant Growth Regul 1998, 24:203-210.
36. Shibata K. Spectroscopic studies on chlorophyll formation in intact leaves. J Biochem 1957, 44:147-173.
37. Skribanek A., Solymosi K., Hideg É., Böddi B. Light and temperature regulation of greening in dark-grown ginkgo (Ginkgo biloba L.). Physiol Plant 2008, 134:649-659.
38. Smeller L., Solymosi K., Fidy J., Böddi B. Activation parameters of the blue shift (Shibata shift) subsequent to protochlorophyllide phototransformation. Biochim Biophys Acta 2003, 1651:130-138.
39. Solymosi K., Böddi B. Optical properties of bud scales and protochlorophyll(ide) forms in leaf primordia of closed and opened buds. Tree Physiol 2006, 26:1075-1085.
40. Solymosi K., Schoefs B. Prolamellar body: a unique plastid compartment, which does not only occur in dark-grown leaves. Plant cell organelles - selected topics 2008, 151-202. Research Sign Post, Kerala. B. Schoefs (Ed.).
41. Solymosi K., Schoefs B. Etioplast and etio-chloroplast formation under natural conditions - the dark side of chlorophyll biosynthesis. Photosynth Res 2010, 105:143-166.
42. Solymosi K., Martinez K., Kristóf Z., Sundqvist C., Böddi B. Plastid differentiation and chlorophyll biosynthesis in different leaf layers of white cabbage (Brassica oleracea cv. capitata). Physiol Plant 2004, 121:520-529.
43. Solymosi K., Bóka K., Böddi B. Transient etiolation: protochlorophyll(ide) and chlorophyll forms in differentiating plastids of closed and breaking leaf buds of horse chestnut (Aesculus hippocastanum). Tree Physiol 2006, 26:1087-1096.
44. 2+. Plant Biol 2006, 8:627-635.
45. Solymosi K., Smeller L., Ryberg M., Sundqvist C., Fidy J., Böddi B. Molecular rearrangement in POR macrodomains as a reason for the blue shift of chlorophyllide fluorescence observed after phototransformation. Biochim Biophys Acta 2007, 1768:1650-1658.
46. Solymosi K., Morandi D., Bóka K., Böddi B., Schoefs B. Plastids, photosynthetic pigments and pigment forms in leaf primordia of buds with various structures and different developmental stages. Planta 2012, 235:1035-1049.
47. Tuba Z., Lichtenthaler H.K., Csintalan Z., Pócs T. Regreening of desiccated leaves of the poikilochlorophyllous Xerophyta scabrida upon re-hydration. J Plant Physiol 1993, 142:103-108.
48. Tuba Z., Lichtenthaler H.K., Maróti I., Csintalan Z. Resynthesis of thylakoids and chloroplast ultrastructure in the desiccated leaves of the poikilochlorophyllous plant Xerophyta scabrida upon re-hydration. J Plant Physiol 1993, 142:742-748.
49. 2 assimilation upon rehydration of the desiccated poikilochlorophyllous plant Xerophyta scabrida (Pax) Th. Dur. et Schinz. Planta 1994, 192:414-420.
50. 2 assimilation and respiration in the poikilochlorophyllous plant Xerophyta scabrida during desiccation. Physiol Plant 1996, 96:383-388.
51. 2 concentration. J Plant Physiol Biochem 1997, 35:381-386.
52. Vassiljev J.M. über den Wasserhaushalt von Pflanzen der Sandwüste im sudöstliche Kara-Kum. Planta 1931, 14:225-309.
53. Whatley J.M. Variations in the basic pathway of chloroplast development. New Phytol 1977, 78:407-420.
54. Whatley J.M. Plastid development in the primary leaf of Phaseolus vulgaris: variations between different types of cell. New Phytol 1979, 82:1-10.
55. Wiktorsson B., Engdahl S., Zhong L.B., Böddi B., Ryberg M., Sundqvist C. The effect of cross-linking of the subunits of NADPH:protochlorophyllide oxidoreductase on the aggregational state of protochlorophyllide. Photosynthetica 1993, 29:205-218.