Disintegration of the prolamellar body structure at high concentrations of Hg2+

Plant Biology

Volumn 8, Issue 5, 2006, Pages 627-635

  Solymosi, K ^a   Mysliwa Kurdziel B ^b   Boka K ^a   Strzalka K ^b   Boddi B ^a  

^a EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^b JAGIELLONIAN UNIVERSITY   (Poland)

Author keywords

Chlorophyllide; Hg2+; Prolamellar body; Protochlorophyllide; Shibata shift

Indexed keywords

MERCURY;

BIOASSAY; BODY SIZE; CONCENTRATION (COMPOSITION); ENZYME; LEAF; MERCURY (ELEMENT); WHEAT;

ARTICLE; DOSE RESPONSE; DRUG EFFECT; PLANT LEAF; ULTRASTRUCTURE; WHEAT;

DOSE-RESPONSE RELATIONSHIP, DRUG; MERCURY; PLANT LEAVES; TRITICUM;

TRITICUM AESTIVUM;

EID: 33749447281     PISSN: 14358603     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-924110     Document Type: Article

References (60)

1. Böddi, B., Lindsten, A., Ryberg, M., and Sundqvist, C. (1989) On the aggregational states of protochlorophyllide and its protein complexes in wheat etioplasts. Physiologia Plantarum 76, 135-143.
2. Böddi, B., Lindsten, A., Ryberg, M., and Sundqvist, C. (1990) Phototransformation of aggregated forms of protochlorophyllide in isolated etioplast inner membranes. Photochemistry and Photobiology 52, 83-87.
3. Böddi, B., Oravecz, A. R., and Lehoczki, E. (1995) Effect of cadmium on organization and photoreduction of protochlorophyllide in dark-grown leaves and etioplast inner membrane preparations of wheat. Photosynthetica 31, 411-420.
4. Böddi, B., Ryberg, M., and Sundqvist, C. (1992) Identification of four universal protochlorophyllide forms in dark-grown leaves by analyses of the 77 K fluorescence emission spectra. Journal of Photochemistry and Photobiology, B: Biology 12, 389-401.
5. Boening, D. W. (2000) Ecological effects, transport, and fate of mercury: a general review. Chemosphere 40, 1335-1351.
6. Butler, W. L. and Briggs, W. R. (1966) The relation between structure and pigments during the first stages of proplastid greening. Biochimica et Biophysica Acta 112, 45-53.
7. Cho, U. H. and Park, J. O. (2000) Mercury-induced oxidative stress in tomato seedlings. Plant Science 156, 1-9.
8. Domanskii, V. P. and Rüdiger, W. (2001) On the nature of the two pathways in chlorophyll formation from protochlorophyllide. Photosynthesis Research 68, 131-139.
9. Domanskii, V. P., Rassadina, V., Gus-Mayer, S., Wanner, G., Schoch, S., and Rüdiger, W. (2003) Characterization of two phases of chlorophyll formation during greening of etiolated barley leaves. Planta 216, 475-483.
10. Eullaffroy, P., Salvetat, R., Franck, F., and Popovic, R. (1995) Temperature dependence of chlorophyll(ide) spectral shifts and photoactive protochlorophyllide regeneration after flash in etiolated barley leaves. Photochemistry and Photobiology 62, 751-756.
11. + and protochlorophyllide-NADPH complexes and their regeneration after flash illumination in leaves and etioplast membranes of dark-grown wheat. Photosynthesis Research 59, 53-61.
12. 688,678 in illuminated etiolated bean leaves. Photobiochemistry and Photobiophysics 8, 85-96.
13. Franck, F. and Mathis, P. (1980) A short-lived intermediate in the photoenzymatic reduction of protochlorophyll(ide) into chlorophyll(ide) at a physiological temperature. Photochemistry and Photobiology 32, 799-803.
14. Goedheer, J. C. (1966) Visible absorption and fluorescence of chlorophyll and its aggregates in solution. In The Chlorophylls (Vernon, L. P. and Seely, G. R., eds.), New York, Boston: Academic Press, pp.147-184.
15. Gunning, B. E. S. (1965) The greening process in plastids. 1. The structure of the prolamellar body. Protoplasma 60, 111-130.
16. Gunning, B. E. S. (2001) Membrane geometry of "open" prolamellar bodies. Protoplasma 215, 4-15.
17. Henningsen, K. W. (1970) Macromolecular physiology of plastids VI. Changes in membrane structure associated with shifts in the absorption maxima of the chlorophyllous pigments. Journal of Cell Science 7, 587-621.
18. Henningsen, K. W. and Boynton, J. E. (1969) Macromolecular physiology of plastids. VII. The effect of brief illumination on plastids of dark-grown barley leaves. Journal of Cell Science 5, 757-793.
19. Henningsen, K. W., Kahn, A., and Houssier, C. (1973) Circular dichroism of protochlorophyllide and chlorophyllide holochrome subunit. FEBS Letters 37, 103-108.
20. Kahn, A., Boardman, N. K., and Thorne, S. W. (1970) Energy transfer between protochlorophyllide molecules: evidence for multiple chromophores in the photoactive protochlorophyllide-protein complex in vivo and in vitro. Journal of Molecular Biology 48, 85-101.
21. Kis-Petik, K., Böddi, B., Kaposi, A. D., and Fidy, J. (1999) Protochlorophyllide forms and energy transfer in dark-grown wheat leaves. Studies by conventional and laser excited fluorescence spectroscopy between 10 K-100 K. Photosynthesis Research 60, 87-98.
22. Klockare, B. and Virgin, H. I. (1983) Chlorophyll(ide) forms after partial phototransformation of protochlorophyll(ide) in etiolated wheat leaves. Physiologia Plantarum 57, 28-34.
23. Le Lay, P., Böddi, B., Kovacevic, D., Juneau, P., Dewez, D., and Popovic, R. (2001) Spectroscopic analysis of desiccation-induced alterations of the chlorophyllide transformation pathway in etiolated barley leaves. Plant Physiology 127, 202-211.
24. Lenti, K., Fodor, F., and Böddi, B. (2002) Mercury inhibits the activity of the NADPH : protochlorophyllide oxidoreductase (POR). Photosynthetica 40, 145-151.
25. Lindsten, A., Wiktorsson, B., Ryberg, M., and Sundqvist, C. (1993) Chlorophyll synthetase activity is relocated from transforming prolamellar bodies to developing thylakoids during irradiation of dark-grown wheat. Physiologia Plantarum 88, 29-36.
26. Masuda, T. and Takamiya, K. (2004) Novel insights into the enzymology, regulation and physiological functions of light-dependent protochlorophyllide oxidoreductase in angiosperms. Photosynthesis Research 81, 1-29.
27. Murakami, S., Yamada, N., Nagano, M., and Osumi, M. (1985) Three dimensional structure of the prolamellar body in squash etioplasts. Protoplasma 128, 147-156.
28. Myśliwa-Kurdziel, B., Franck, F., Ouazzani-Chahdi, M. A., and Strzałka, K. (1999) Changes in endothermic transitions associated with light-induced chlorophyllide formation, as investigated by differential scanning calorimetry. Physiologia Plantarum 107, 230-239.
29. Myśliwa-Kurdziel, B. and Strzałka, K. (2002) Influence of metals on biosynthesis of photosynthetic pigments. In Physiology and Biochemistry of Metal Toxicity and Tolerance in Plants (Prasad, M. N. V. and Strzałka, K., eds.), Dordrecht, Boston, London: Kluwer Academic Publishers, pp.201-227.
30. Myśliwa-Kurdziel, B. and Strzałka, K. (2005) Influence of Cd(II), Cr(VI) and Fe(III) on early steps of deetiolation process in wheat: fluorescence spectral changes of protochlorophyllide and newly formed chlorophyllide. Agriculture, Ecosystems and Environment 106, 199-207.
31. Nyitrai, P., Bóka, K., Gáspár, L., Sárvári, É., Lenti, K., and Keresztes, Á. (2003) Characterization of the stimulating effect of low-dose stressors in maize and bean seedlings. Journal of Plant Physiology 160, 1175-1183.
32. Ouazzani-Chahdi, M. A., Schoefs, B., and Franck, F. (1998) Isolation and characterisation of photoactive complexes of NADPH : protochlorophyllide oxidoreductase from wheat. Planta 206, 673-680.
33. 2+ on growth and metabolism of cabbage. Plant Science 163, 753-758.
34. Patra, M. and Sharma, A. (2000) Mercury toxicity in plants. Botanical Review 66, 379-422.
35. Poirier, I., and Bertrand, M. (2005) Photosynthetic organisms and excess of metals. Photosynthetica 43, 345-353.
36. Prasad, D. D. K. and Prasad, A. R. K. (1987a) Effect of lead and mercury on chlorophyll synthesis in mung bean seedlings. Phytochemistry 26, 881-883.
37. Prasad, D. D. K. and Prasad, A. R. K. (1987b) Altered delta-aminolevulinic acid metabolism by lead and mercury in germinating seedlings of bajra (Pennisetum typhoideum). Journal of Plant Physiology 127, 241-249.
38. Rassadina, V., Domanskii, V., Averina, N. G., Schoch, S., and Rüdiger, W. (2004) Correlation between chlorophyllide esterification, Shibata shift and regeneration of protochlorophyllide650 in flash-irradiated etiolated barley leaves. Physiologia Plantarum 121, 556-567.
39. Rüdiger, W. (1997) Chlorophyll metabolism: from outer space down to the molecular level. Phytochemistry 46, 1151-1167.
40. Rüdiger, W., Benz, J., and Guthoff, C. (1980) Detection and partial characterization of activity of chlorophyll synthetase in etioplast membranes. European Journal of Biochemistry 190, 193-200.
41. Ryberg, M. and Dehesh, K. (1986) Localization of NADPH : protochlorophyllide oxidoreductase in dark-grown wheat (Triticum aestivum) by immuno-electron microscopy before and after transformation of the prolamellar bodies. Physiologia Plantarum 66, 616-624.
42. Ryberg, M. and Sundqvist, C. (1982a) Characterization of prolamellar bodies and prothylakoids fractionated from wheat etioplasts. Physiologia Plantarum 56, 125-132.
43. Ryberg, M. and Sundqvist, C. (1982b) Spectral forms of protochlorophyllide in prolamellar bodies and prothylakoids fractionated from wheat etioplasts. Physiologia Plantarum 56, 133-138.
44. Ryberg, M. and Sundqvist, C. (1988) The regular ultrastructure of isolated prolamellar bodies depends on the presence of membrane-bound NADPH-protochlorophyllide oxidoreductase. Physiologia Plantarum 73, 218-226.
45. 2 uptake and water relations of spruce (Picea abies) seedlings. Physiologia Plantarum 69, 265-270.
46. Schoefs, B., Bertrand, M., and Franck, F. (2000) Spectroscopic properties of protochlorophyllide analyzed in situ in the course of etiolation and in illuminated leaves. Photochemistry and Photobiology 72, 85-93.
47. Schoefs, B. (2001) The protochlorophyllide-chlorophyllide cycle. Photosynthesis Research 70, 257-271.
48. Schoefs, B. (2005) Protochlorophyllide reduction - what is new in 2005? Photosynthetica 43, 329-343.
49. Schoefs, B. and Franck, F. (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. Journal of Experimental Botany 44, 1053-1057.
50. Selstam, E., Schelin, J., Brain, T., and Williams, W. P. (2002) The effects of low pH on the properties of protochlorophyllide oxidoreductase and the organization of prolamellar bodies of maize (Zea mays). European Journal of Biochemistry 269, 2336-2346.
51. Shibata, K. (1957) Spectroscopic studies on chlorophyll formation in intact leaves. Journal of Biochemistry 44, 147-173.
52. Smeller, L., Solymosi, K., Fidy, J., and Böddi, B. (2003) Activation parameters of the blue shift (Shibata shift) subsequent to protochlorophyllide phototransformation. Biochimica Biophysica Acta 1651, 130-138.
53. 2+ reacts with different components of the NADPH : protochlorophyllide oxidoreductase macrodomains. Plant Biology 6, 358-368.
54. Sperling, U., Franck, F., van Cleve, B., Frick, G., Apel, K., and Armstrong, G. A. (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.
55. 2+ on the biosynthesis of chlorophyll in leaves of barley. Physiologia Plantarum 63, 293-298.
56. Sundqvist, C. and Dahlin, C. (1997) With chlorophyll pigments from prolamellar bodies to light-harvesting complexes. Physiologia Plantarum 100, 748-759.
57. Wiktorsson, B., Engdahl, S., Zhong, L. B., Böddi, B., Ryberg, M., and Sundqvist, C. (1993) The effect of cross-linking of the subunits of NADPH : protochlorophyllide oxidoreductase on the aggregational state of protochlorophyllide. Photosynthetica 29, 205-218.
58. Wiktorsson, B., Ryberg, M., Cough, S., and Sundqvist, C. (1992) Isoelectric focusing of pigment-protein complexes solubilized from non-irradiated and irradiated prolamellar bodies. Physiologia Plantarum 85, 659-669.
59. Williams, W. P., Selstam, E., and Brain, T. (1998) X-ray diffraction studies of the structural organisation of prolamellar bodies isolated from Zea mays. FEBS Letters 422, 252-254.
60. Willows, R. D. (2003) Biosynthesis of chlorophylls from protoporphyrin IX. Natural Product Reports 20, 327-341.