Death mechanisms caused by carotenoid biosynthesis inhibitors in green and in undeveloped plant tissues

Pesticide Biochemistry and Physiology

Volumn 78, Issue 3, 2004, Pages 127-139

  Kim, Jin Seog ^a   Yun, Byung Wook ^b   Choi, Jung Sup ^a   Kim, Tae Joon ^a   Kwak, Sang Soo ^b   Cho, Kwang Yun ^a  

^a Korea Research Institute of Chemical Technology   (South Korea)

^b Korea Research Institute of Bioscience and Biotechnology (KRIBB)   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ZEA; ZEA MAYS;

EID: 1642323673     PISSN: 00483575     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pestbp.2003.12.001     Document Type: Article

References (51)

1. D. Siefermann-Harms, The light-harvesting and protective functions of carotenoids in photosynthetic membranes, Physiol. Plant 69 (1987) 561.
2. R. Oelmüller, Photooxidative destruction of chloroplasts and its effect on nuclear gene expression and extraplastidic enzyme levels, Photochem. Photobiol. 49 (1989) 229.
3. A. Thiele, K. Schirwitz, K. Winter, G.H. Krause, Increased xanthophyll cycle activity and reduced D1 protein inactivation related to photoinhibition in two plant systems acclimated to excess light, Plant Sci. 115 (1996) 237.
4. M. Havaux, J.-P. Bonfils, C. Ltz, K.K. Niyogi, Photodamage of the photosynthetic apparatus and its dependence on the leaf developmental stage in the npq1 Arabidopsis mutant deficient in the xanthophyll cycle enzyme violaxanthin de-epoxidase, Plant Physiol. 124 (2000) 273.
5. S.P. Mayfield, W.C. Taylor, Carotenoid-deficient maize seedlings fail to accumulate light harvesting chlorophyll a/b binding protein (LHCP) mRNA, Eur. J. Biochem. 144 (1984) 79.
6. K. Humbeck, S. Römer, H. Senger, Evidence for an essencial role of carotenoids in the assembly of an active photosystem II, Planta 179 (1989) 242.
7. T. Markgraf, R. Oelmüller, Evidence that carotenoids are required for the accumulation of a functional photosystem II, but not photosystem I in the cotyledons of mustard seedlings, Planta 185 (1991) 97.
8. A. Trebst, B. Depka, Role of carotene in the rapid turnover and assembly of photosystem II in Chlamydomonas reinhardtii, FEBS Lett. 400 (1997) 359.
9. B. Depka, P. Jahns, A. Trebst, β-Carotene to zeaxanthin conversion in the rapid turnover of the D1 protein of photosystem II, FEBS Lett. 424 (1998) 267.
10. M. Havaux, Carotenoids as membrane stabilizers in chloroplasts, Trends Plant Sci. 3 (1998) 147.
11. M. Wrischer, N. Ljubesic, B. Salopek, The role of carotenoids in the structural and functional stability of thylkoids in plastids of dark-grown spruce seedlings, J. Plant Physiol. 153 (1998) 46.
12. A. Sujak, J. Gabrielska, W. Grudziñsk, R. Borc, P. Mazurek, W.I. Gruszecki, Lutein and zeaxanthin as protectors of lipid membranes against oxidative damage: The structural aspects, Arch. Biochem. Biophys. 371 (1999) 301.
13. K.K. Niyogi, C. Shih, W.S. Chow, B.J. Pogson, D. DellaPenna, O. Björkman, Photoprotection in a zeaxanthin-and lutein-deficient double mutant of Arabidopsis, Photosynth. Res. 67 (2001) 139.
14. P. Böger, Mode of action of herbicides affecting carotenogenesis, J. Pestic. Sci. 21 (1996) 473.
15. S. Jung, J.S. Kim, K.Y. Cho, B.G. Kang, Changes in the pools of carotenoids and protochlorophyll(ide) in etiolated cucumber (Cucumis sativus) cotyledons treated with norflurazon and KC 6361, Photosynthetica 36 (1999) 361.
16. C.H. Foyer, M. Lelandais, K.J. Kunert, Photooxidative stress in plants, Physiol. Plant 92 (1994) 696.
17. G. Bartosz, Oxidative stress in plants, Acta Physiol. Plantarum 19 (1997) 47.
18. F.D. Hess, Light-dependent herbicides: an review, Weed Sci. 48 (2000) 160.
19. J.S. Kim, T.J. Kim, O.K. Kwon, K.Y. Cho, Mechanism of action of sulcotrione in developed plant tissues, BCPC-Weeds 2 (2001) 557.
20. S. Kowalczyk-Schrder, G. Sandmann, Interference of fluridone with the desaturation of phytoene by membranes of the Cyanobacterium aphanocapsa, Pestic. Biochem. Physiol. 42 (1992) 7.
21. H.K. Lichtenthaler, Chlorophylls and carotenoids: pigments of photosynthetic biomembranes, Methods Enzymol. 148 (1987) 350.
22. E. Bernt, H.U. Bergmeyer, Inorganic peroxides, in: H.U. Bergmeyer (Ed.), Method of Enzymatic Analysis, vol. 4, Academic Press, New York, 1974, pp. 2246-2248.
23. M.M. Bradford, A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding, Anal. Biochem. 72 (1976) 284.
24. J.M. McCord, I. Fridovich, Superoxide dismutase: an enzymic function for erythrocuprein, J. Inorg. Biochem. 244 (1969) 6049.
25. S.S. Kwak, S.K. Kim, M.S. Lee, K.H. Jung, I.H. Park, J.R. Liu, Acidic peroxidase from suspension-cultures of sweet potato, Phytochemistry 39 (1995) 981.
26. I.K. Smith, T.L. Vierheller, C.A. Thorne, Assay of glutathione reductase in crude tissue homogenates using 5,5′-dithiobis (2-nitrobenzoic acid), Anal. Biochem. 175 (1988) 408.
27. S.K. Kim, S.S. Kwak, K.H. Jung, S.R. Min, I.H. Park, J.R. Liu, Selection of plant cell lines for high yields of peroxidase, Korean Biochem. J. 27 (1994) 132.
28. M.V. Rao, G. Paliyath, D.P. Ormrod, Ultraviolet-B-and ozone-induced biochemical changes in antioxidant enzymes of Arabidopsis thaliana, Plant Physiol. 110 (1996) 125.
29. B.F. Finckh, K.J. Kunert, Vitamine C and E: an antioxidative system against herbicide induced lipid peroxidation in higher plants, J. Agric. Food Chem. 33 (1985) 574.
30. M.Y. Law, S.A. Charles, B. Halliwell, Glutathione and ascorbic acid in spinach (Spinacea oleracea) chloroplasts. The effect of hydrogen peroxide and of paraquat, Biochem. J. 210 (1983) 899.
31. J.A. Buege, S.D. Aust, Microsomal lipid peroxidation, Methods Enzymol. 52 (1978) 302.
32. D.L. Morris, Quantitative determination of carbohydrates with Drywood's anthrone reagent, Science 107 (1948) 254.
33. W. Van Camp, C. Bowler, R. Villarroel, E.W.T. Tsang, M. Van Montagu, D. Inze, Characterization of iron superoxide dismutase cDNAs from plants obtained by genetic complementation in Escherichia coli, Proc. Natl. Acad. Sci. USA 87 (1990) 9903.
34. J.-S. Kim, S. Jung, I.T. Hwang, K.Y. Cho, Characteristics of chlorophyll a fluorescence induction in cucumber cotyledons treated with diuron, norflurazon, and sulcotrione, Pestic. Biochem. Physiol. 65 (1999) 73.
35. N.L. Rocca, F.D. Vecchia, R. Barbato, A. Bonora, E. Bergantino, N. Rascio, Plastid photodamage and Cab gene expression in barley leaves. Physiol. Plantarum 109 (2000) 51.
36. F.-A. Wollman, L. Minai, R. Nechushtai, The biogenesis and assembly of photosynthetic proteins in thylakoid membranes, Biochim. Biophys. Acta 1411 (1999) 21.
37. J.C. Tonkyn, X.-W. Deng, W. Gruissem, Regulation of plastid gene expression during photooxidative stress, Plant Physiol. 99 (1992) 1406.
38. J. Kim, L.A. Eichacker, W. Rüdiger, J.E. Mullet, Chlorophyll regulates accumulation of the plastid-encoded chlorophyll proteins P700 and D1 by increasing apoprotein stability, Plant Physiol. 104 (1994) 907.
39. H. Thomas, Chlorophyll: a symptom and a regulator of plastid development, New Phytol. 136 (1997) 163.
40. S. Rodermel, Pathways of plastid-to-nucleus signaling, Trends Plant Sci. 6 (2001) 471.
41. G.T. Jahoubjan, I.N. Minkov, Enhanced chlorophyllide accumulation after flash irradiation of etiolated wheat plants treated with SAN-9789, J. Plant Physiol. 151 (1997) 649.
42. Z. Cohen, Y.M. Heimer. Δ6 Desaturase inhibiton: a novel mode of action of norflurazon, Plant Physiol. 93 (1990) 347.
43. J. Kurepa, D. Hrouart, M.V. Montagu, D. Inz, Differential expression of CuZn-and Fe-superoxide dismutase genes of tobacco during deveopment, oxidative stress, and hormonal treatments, Plant Cell Physiol. 38 (1997) 463.
44. G. Gullner, A.D. Dodge, Effect of singlet oxygen generation substances in the ascorbic acid and glutathione content in pea leaves, Plant Sci. 154 (2000) 127.
45. S. Jung, J.-S. Kim, K.Y. Cho, B.G. Kang, Antioxidant responses of cucumber (Cucumis sativus) to photoinhibition and oxidative stress induced by norflurazon under high and low PPFD's, Plant Sci. 153 (2000) 145.
46. S.J. Stegink, K.C. Vaughn, Norflurazon (SAN-9789) reduces abscisic acid levels in cotton seedlings: a glandless isoline is more sensitive than its glanded counterpart, Pestic. Biochem. Physiol. 31 (1988) 269.
47. M. Seo, T. Koshiba, Complex regulation of ABA biosynthesis in plants, Trends Plant Sci. 7 (2002) 41.
48. S. Aubert, E. Gout, R. Bligny, D. Marty-Mazars, F. Barrieu, J. Alabouvette, F. Marty, R. Douce, Ultrastructural and biochemical characterization of autophagy in higher plant cells subjected to carbon deprivation: control by the supply of mitochondria with respiratory substrates, J. Cell Biol. 133 (1996) 1251.
49. S.-M. Yu, Cellular and genetic responses of plants to sugar starvation, Plant Physiol. 121 (1999) 687.
50. S. Smeekens, Sugar-induced signal transduction in plants, Annu. Rev. Plant Physiol. Plant Mol. Biol. 51 (2000) 49.
51. S.-L. Ho, Y.-C. Chao, W.-F. Tong, S.-M. Yu, Sugar coordinately and differentially regulates growth-and stress-related gene expression via a complex signal transduction network and multiple control mechanisms, Plant Physiol. 125 (2001) 877.