Lipophilic Molecules as a Part of Antioxidant System in Plants

Oxidative Damage to Plants: Antioxidant Networks and Signaling

Volumn , Issue , 2014, Pages 321-344

  Szymanska, Renata ^a   Latowski, Dariusz ^a   Nowicka, Beatrycze ^a   Strzalka, Kazimierz ^a  

^a JAGIELLONIAN UNIVERSITY   (Poland)

Author keywords

Antioxidants; Lipid Peroxidation; Plastochromanol; Reactive Oxygen Species; Signaling Pathways; Tocochromanols; Tocopherols

Indexed keywords

EID: 84902403449     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-12-799963-0.00010-1     Document Type: Chapter

References (121)

1. Abbasi A.R., Hajirezaei M., Hofius D., Sonnevald U., Voll L.M. Specific roles of αα-and γ-tocopherol in biotic stress responses of transgenic tobacco. Plant Physiol. 2007, 143:1720-1738.
2. Apel K., Hirt H. Reactive oxygen species: metabolism, oxidative stress and signal transduction. Annu. Rev. Plant Biol. 2004, 55:373-399.
3. Aro E.M., Virgin I., Andersson B. Photoinhibition of photosystem II: inactivation, protein damage and turnover. Biochim. Biophys. Acta. 1993, 1143:113-134.
4. Asada K. The water-water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1999, 50:601-639.
5. Asada K. Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol. 2006, 141:391-396.
6. Bell E., Takeda S., Dolan L. Reactive oxygen species in growth and development. Signaling and Communication in Plants 2009, 43-53. Springer-Verlag, Berlin. L.A. Rio, A. Puppo (Eds.).
7. Cahoon E.B., Hall S.H., Ripp K.G., Ganzke T.S., Hitz W.D., Coughlan S.J. Metabolic redesign of vitamin E biosynthesis in plants for tocotrienol production and increased antioxidant content. Nat. Biotechnol. 2003, 21:1082-1087.
8. Caretto S., Paradiso A., D'Amico L., Gara L.D. Ascorbate and gluthatione metabolism in two sunflower cell lines of differing α-tocopherol biosynthetic capability. Plant Physiol. Biochem. 2002, 40:509-513.
9. Cela J., Falk J., Munné-Bosch S. Ethylene signaling may be involved in the regulation of tocopherol biosynthesis in Arabidopsis thaliana. FEBS Lett. 2009, 583:992-996.
10. Cela J., Chang C., Munné-Bosch S. Accumulation of γ- rather than α-tocopherol alters ethylene signaling gene expression in the vte4 mutant of Arabidopsis thaliana. Plant Cell Physiol. 2011, 52:1389-1400.
11. Chen D.F., Zhang M., Wang Y.Q., Chen X.W. Expression of γ-tocopherol methyltransferase gene from Brassica napus increased α-tocopherol content in soybean seed. Biol Plant. 2012, 56:131-134.
12. Choudhury S., Panda P., Sahoo L., Panda S.K. Reactive oxygen species signaling in plants under abiotic stress. Plant Signal. Behav. 2013, 8:e23681.
13. Collakova E., DellaPenna D. Isolation and functional analysis of homogentisite phytyltransferase from Synechocystis sp. PC6803 and Arabidopsis. Plant Physiol. 2001, 127:1113-1124.
14. Collakova E., DellaPenna D. Homogentisate phytyltransferase activity is limiting for tocopherol biosynthesis in Arabidopsis thaliana. Plant Physiol. 2003, 131:632-642.
15. Collin V.C., Eymery F., Genty B., Rey P., Havaux M. Vitamin E is essential for the tolerance of Arabidopsis thaliana to metal induced oxidative stress. Plant Cell Environ. 2008, 31:99-111.
16. Dahnhardt D., Falk J., Appel J., van der Kooij T.A.W., Schulz-Friedrich R., Krupinska K. The hydroxyphenylpyruvate dioxygenase from Synechocystis sp. PCC 6803 is not required for plastoquinone biosynthesis. FEBS Lett. 2002, 523:177-181.
17. Davletova S., Rizhsky L., Liang H., Shengqiang Z., Oliver D.J., Coutu J., et al. Cytosolic ascorbate peroxidase 1 is a crucial component of the reactive oxyen gene network of Arabidopsis. Plant Cell 2005, 17:268-281.
18. DellaPenna D. A decade of progress in understanding vitamin E synthesis. J. Plant Physiol. 2005, 162:729-737.
19. DellaPenna D., Pogson B.J. Vitamin synthesis in plants: tocopherols and carotenoids. Annu. Rev. Plant Biol. 2006, 57:711-738.
20. Ellouzi H., Hamed K.B., Cela J., Munne-Bosch S., Abdelly C. Early effects of salt stress on the physiological and oxidative status of Cakile maritima (halophyte) and Arabidopsis thaliana (glycophyte). Physiol. Plant. 2011, 142:128-143.
21. Evans N.H., McAinsh M.R., Hetherington A.M., Knight M.R. ROS perception in Arabidopsis thaliana: the ozone-induced calcium response. Plant J. 2005, 41:615-626.
22. Falk J., Krauss N., Dahnhardt D., Krupinska K. The senescence associated gene of barley encoding 4-hydroxyphenylpyruvate dioxygenase is expressed during oxidative stress. J. Plant Physiol. 2002, 159:1245-1253.
23. Farre G., Sudhakar D., Naqvi S., Sandmann G., Christou P., Capell T., et al. Transgenic rice grains expressing a heterologous p-hydroxyphenylpyruvate dioxygenase shift tocopherol synthesis from the γ- to the α-isoform without increasing absolute tocopherols levels. Transgenic Res. 2012, 21:1093-1097.
24. Fey V., Wagner R., Brautigam K., Pfannschmidt T. Photosynthetic redox control of nuclear gene expression. J. Exp. Bot. 2005, 56:1491-1498.
25. Fischer B.B., Hideg É., Krieger-Liszkay A. Production, detection, and signaling of singlet oxygen in photosynthetic organisms. Antiox. Redox Signal. 2013, 18:2145-2162.
26. Foyer C.H., Noctor G. Redox sensing and signaling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiol. Plant. 2003, 119:355-364.
27. Foyer C.H., Noctor G. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 2005, 17:1866-1875.
28. Foyer C.H., Shigeoka S. Understanding oxidative stress and antioxidant function to enhance photosynthesis. Plant Physiol. 2011, 155:93-100.
29. Galvez-Vadivieso G., Mullineaux P.M. The role of reactive oxygen species in signaling from chloroplasts to the nucleus. Plant Physiol. 2010, 138:430-439.
30. Garcia I., Rodgers M., Lenne C., Rolland A., Sailland A., Matringe M. Subcellular localization and purification of a p-hydroxyphenylpyruvate dioxygenase from cultured carrot cells and characterization of the corresponding cDNA. Biochem. J. 1997, 325:761-769.
31. Gechev T.S., van Breusegem F., Stone J.M., Denev I., Laloi C. Reactive oxygen species as signals that modulate plant stress responses and programmed cell death. BioEssay 2006, 28:1091-1101.
32. Giordano M., Chen Y.B., Koblizek M., Falkowski P.G. Regulation of nitrate reductase in Chlamydomonas reinhardtii by the redox state of the plastoquinone pool. Eur. J. Phycol. 2005, 40:345-352.
33. Gruszka J., Kruk J. RP-LC for determination of plastochromanol, tocotrienols and tocopherols in plant oils. Chromatographia 2007, 66:909-913.
34. Halliwell B. Reactive species and antioxidants. Redox biology is a fundamental theme of aerobic life. Plant Physiol. 2006, 141:312-322.
35. Havaux M., Eymery F., Porfirova S., Rey P., Dormann P. Vitamin E protects against photo-inhibition and photooxidative stress in Arabidopsis thaliana. Plant Cell 2005, 17:3451-3469.
36. Hofius D., Hajirezaei M., Geiger M., Tschiersch H., Meizer M., Sonnewald U. RNAi-mediated tocopherol deficiency impairs photoassimilate export in transgenic potato plants. Plant Physiol. 2004, 135:1256-1268.
37. Inoue S., Ejima K., Iwai E., Hayashi H., Appel J., Tyystjärvi E., et al. Protection by α-tocopherol of the repair of photosystem II during photoinhibition in Synechocystis sp. PCC 6803. Biochim. Biophys. Acta 2011, 1807:236-241.
38. Kalyanaraman B., Darley-Usmar V., Davies K.J., Dennery P.A., Forman H.J., Grisham M.B., et al. Measuring reactive oxygen and nitrogen species with fluorescent probes: challenges and limitations. Free Radic. Biol. Med. 2012, 52:1-6.
39. Kanwischer M., Porforova S., Bergmuller E., Dormann P. Alternation of tocopherol cyclase activity in transgenic and mutant plants of Arabidopsis affect tocopherol content, tocopherol composition and oxidative stress. Plant Physiol. 2005, 137:713-723.
40. Karpinski S., Reynolds H., Karpinska B., Wingsle G., Creissen G., Mullineaux P.M. Systemic signaling and acclimation in response to excess excitation energy in Arabidopsis. Science 1999, 284:654-657.
41. Krause G.H., Winter K., Matsubara S., Krause B., Jahns P., Virgo A., et al. Photosynthesis, photoprotection, and growth of shade-tolerant tropical tree seedlings under full sunlight. Photosynth. Res. 2012, 113:273-285.
42. Kreslavsky V.D., Los D.A., Allakhverdiev S.I., Kuznetsov V.I.V. Signaling role of reactive oxygen species in plants under stress. Russ. J. Plant Physiol. 2012, 59:141-154.
43. Kriger-Liszkay A. Singlet oxygen production in photosynthesis. J. Exp. Bot. 2005, 56:337-346.
44. Kruk J., Strzałka K. Occurrence and function of α-tocopherol quinone in plants. J. Plant Physiol. 1995, 145:405-409.
45. Kruk J., Trebst A. Plastoquinol as a singlet oxygen scavenger in photosystem II. Biochim. Biophys. Acta 2008, 1777:154-162.
46. Kruk J., Hollander-Czytko H., Oettmeier W., Trebst A. Tocopherol as a singlet oxygen scavenger in photosystem II. J. Plant Physiol. 2005, 162:749-757.
47. Kusmic C., Barsacchi R., Barsanti L., Gualtieri P., Passarelli V. Euglena gracilis as source of the antioxidant vitamin E. Effects of culture conditions in the wild strain and in the natural mutant WZSL. J. App. Phycol. 1999, 10:555-559.
48. Lepetit B., Sturm S., Rogato A., Gruber A., Sachse M., Falciatore A., et al. High light acclimation in the secondary plastids containing diatom Phaeodactylum tricornutum is triggered by the redox state of the plastoquinone pool. Plant Physiol. 2013, 161:853-865.
49. Li Y., Wang Z., Sun X., Tang K. Current opinions on the functions of tocopherol based on the genetic manipulation of tocopherol biosynthesis in plants. J. Integr. Plant Biol. 2008, 50:1057-1069.
50. Li Z., Keasling J.D., Niyogi K.K. Overlapping photoprotective function of vitamin E and carotenoids in Chlamydomonas. Plant Physiol. 2012, 158:313-323.
51. Liu X., Hua X., Guo J., Qi D., Wang L., Liu Z., et al. Enhanced tolerance to drought stress in transgenic tobacco plants overexpressing VTE1 for increased tocopherol production from Arabidopsis thaliana. Biotechnol. Lett. 2008, 30:1275-1280.
52. Lushchak V.I., Semchuk N.M. Tocopherol biosynthesis: chemistry, regulation and effects of environmental factors. Acta Physiol. Plant 2012, 34:1607-1628.
53. Maeda H., DellaPenna D. Tocopherol functions in photosynthetic organisms. Curr. Opin. Plant Biol. 2007, 10:260-265.
54. Maeda H., Song W., Sage T.L., DellaPenna D. Tocopherols play a crucial role in low-temperature adaptation and phloem loading in Arabidopsis. Plant Cell 2006, 18:2710-2732.
55. Marder J.B., Droppa M., Caspi V., Raskin V.I., Horvath G. Light-dependent thermoluminescence from thylakoids from greening barely leaves: evidence for involvement of oxygen radicals and free chlorophyll. Physiol. Plant. 1998, 104:713-719.
56. Mene-Saffrane L., DellaPenna D. Biosynthesis, regulation and functions of tocochromanols in plants. Plant Physiol. Biochem. 2010, 48:301-309.
57. Mene-Saffrane L., Jones A.D., DellaPenna D. Plastochromanol-8 and tocopherols are essential lipid-soluble antioxidants during seed desiccation and quiescence in Arabidopsis. Proc. Natl. Acad. Sci. USA 2010, 107:17815-17820.
58. Miller G., Shulaev V., Mittler R. Reactive oxygen signaling and abiotic stress. Physiol. Plant. 2008, 133:481-489.
59. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 2002, 7:405-410.
60. Mittler R., Vanerauwera S., Gollery M., Van Breusegem F. Reactive oxygen network of plants. Trends Plant Sci. 2004, 9:490-498.
61. Mullineaux P., Ball L., Escobar C., Karpinska B., Creissen G., Karpinski S. Are diverse signaling pathways integrated in the regulation of Arabidopsis antioxidant defense gene expression in response to excess excitation energy?. Phil. Trans. R. Soc. Lond. B 2000, 355:1531-1540.
62. Munné-Bosch S. The role of α-tocopherol in plant stress tolerance. J. Plant Physiol. 2005, 162:743-748.
63. Munné-Bosch S. Alpha-tocopherol: a multifaceted molecule in plants. Vitam. Horm. 2007, 76:375-392.
64. Munne-Bosch S., Alegre L. The function of tocopherols and tocotrienols in plants. Crit. Rev. Plant Sci. 2002, 21:31-57.
65. Munné-Bosch S., Weiler E., Alegre L., Muller M., Duchting P., Falk J. α-Tocopherol may influence cellular signaling by modulating jasmonic acid levels in plants. Planta 2007, 225:681-691.
66. Nishiyama Y., Allakhverdiev S., Murata N. A new paradigm for the action of reactive oxygen species in the photo-inhibition of photosystem II. Biochim. Biophys. Acta 2006, 1757:742-749.
67. Norris S.R., Shen X., DellaPenna D. Complementation of the Arabiopsis pds1 mutation with the gene encoding p-hydroxyphenylpyruvate dioxygenase. Plant Physiol. 1998, 117:1317-1323.
68. Nowicka B., Kruk J. Occurrence, biosynthesis and function of isoprenoid quinones. Biochim. Biophys. Acta 2010, 1797:1587-1605.
69. Nowicka B., Kruk J. Plastoquinol is more active than α-tocopherol in singlet oxygen scavenging during high light stress of Chlamydomonas reinhardtii. Biochim. Biophys. Acta 2012, 1817:389-394.
70. Nowicka B., Gruszka J., Kruk J. Function of plastochromanol and other biological prenyllipids in the inhibition of lipid peroxidation - a comparative study in model systems. Biochim. Biophys. Acta 2013, 1828:233-240.
71. Op den Camp R.G.L., Przybyla D., Ochsenbein C., Laloi C., Kim C., Danon A., et al. Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis. Plant Cell 2003, 15:2320-2332.
72. O'Brien J., Daudi A., Butt V.S., Bolwell G.P. Reactive oxygen species and their role in plant defense and cell wall metabolism. Planta 2012, 236:765-779.
73. Petrov V., Schippers J., Benina M., Minkov I., Mueller-Roeber B., Gechev T. In search for new players of the oxidative stress network by phenotyping an Arabidopsis T-DNA mutant collection on reactive oxygen species-eliciting chemicals. Plant Omics J. 2013, 6:46-54.
74. Pfannschmidt T., Nilsson A., Allen J.F. Photosynthetic control of chloroplast gene expression. Nature 1999, 397:625-628.
75. Piller L.E., Abraham M., Dörmann P., Kessler F., Besagni C. Plastid lipid droplets at the crossroads of prenylquinone metabolism. J. Exp. Bot. 2012, 63:1609-1618.
76. Porfirova S., Bergmuller E., Tropf S., Lemke R., Dormann P. Isolation of an Arabidopsis mutant lacking vitamin E and identification of cyclase essential for tocopherol biosynthesis. Proc. Natl. Acad. Sci. USA 2002, 99:12495-12500.
77. Pospisil P. Production of reactive oxygen species by Photosystem II. Biochim. Biophys. Acta 2009, 1787:1151-1160.
78. Provencher L.M., Miao L., Sinha N., Lucas W.J. Sucrose export defective1 encodes a novel protein implicated in chloroplast-to-nucleus signaling. Plant Cell 2001, 13:1127-1141.
79. Rastogi A., Yadav D.K., Szymanska R., Kruk J., Sedlarova M., Pospisil P. Singlet oxygen scavenging activity of tocopherol and plastochromanol in Arabidopsis thaliana: relevance to photooxidative stress. Plant Cell Environ. 2013, 10.1111/pce.12161.
80. Rautenkranz A.A.F., Li L., Mauchler F., Mautinoia E., Oertli J.J. Transport of ascorbic acid and dehydroascorbic acids across protoplast and vacuole membranes isolated from barley (Hordeum vulgare L. cv Gerbel) leaves. Plant Physiol. 1994, 106:187-193.
81. Riewe D., Koohi M., Lisec J., Pgeiffer M., Lippmann R., Schmeiche J., et al. A tyrosine aminotransferase involved in tocopherol synthesis in Arabidopis. Plant J. 2012, 71:850-859.
82. Rizhsky L., Hallak-Herr E., van Breusegem F., Rachmilevitch S., Barr J.E., Rodermel S., et al. Double antisense plants lacking ascorbate peroxidase and catalase are less sensitive to oxidative stress than single antisense plants lacking ascorbate peroxidase or catalase. Plant J. 2002, 32:329-342.
83. Rochaix J.D. Redox regulation of thylakoid protein kinases and photosynthetic gene expression. Antiox. Redox Signal. 2013, 18:2184-2201.
84. Rochaix J.D., Lemeille S., Shapiguzov A., Samol I., Fucile G., Willig A., et al. Protein kinases and phosphatases involved in the acclimation of the photosynthetic apparatus to a changing light environment. Phil. Trans. R. Soc. Lond. B 2012, 367:3466-3474.
85. Sadre R., Pfaff C., Buchkremer S. Plastoquinone-9 biosynthesis in cyanobacteria differs from that in plants and involves a novel 4-hydroxybenzoate solanesyltransferase. Biochem. J. 2012, 442:621-629.
86. 6f complex from Bryopsis corticulans as detected by EPR spectroscopy. Biophys. Chem. 2009, 146:7-12.
87. Sattler S.E., Cahoon E.B., Coughlan S.J., DellaPenna D. Characterization of tocopherol cyclase from higher plants and cyanobacteria. Evolutionary implications for tocopherol synthesis and function. Plant Physiol. 2003, 132:2184-2195.
88. Sattler S.E., Gilliland L.U., Magallanes-Lundback M., Pollard M., DellaPenna D. Vitamin E is essential for seed longevity and for preventing lipid peroxidation during germination. Plant Cell 2004, 16:1419-1432.
89. Sattler S.E., Mene-Saffrane L., Farmer E.E., Krischke M., Mueller M.J., DellaPenna D. Non-enyzmatic lipid peroxidation reprograms gene expression and activates defense markers in Arabidopsis tocopherol-deficient mutans. Plant Cell 2006, 18:3706-3720.
90. Scheler C., Durner J., Astier J. Nitric oxide and reactive oxygen species in plant biotic interactions. Curr. Opin. Plant Biol. 2013, doi:org/10.1016/j.pbi.2013.06.020.
91. Schmidt K., Fufezan C., Kriger-Liszkay A., Satoh H., Paulsen H. Recombinant water-soluble chlorophyll protein from Brassica oleracea var. botrys binds various chlorophyll derivatives. Biochemistry 2003, 42:7427-7433.
92. Schneider C. Chemistry and biology of vitamin E. Mol. Nutr. Food Res. 2005, 49:7-30.
93. Semchuk N.M., Lushchak O.V., Falk J., Krupinska K., Lushchak V.I. Inactivation of genes, encoding tocopherol biosynthetic pathway enzymes, results in oxidative stress in outdoor grown Arabidopsis thaliana. Plant Physiol. Biochem. 2009, 47:384-390.
94. Sharma P., Jha A.B., Dubey R.S., Pessarakli M. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J. Bot. 2012, 2012. http://dx.doi.org/10.1155/2012/217037.
95. Shigeoka S., Onishi T., Nakano Y., Kitaoka S. The contents and subcellular distribution of tocopherols in Euglena gracilis. Agric. Biol. Chem. 1986, 50:1063-1065.
96. Shintani D., DellaPenna D. Elevating the vitamin E content of plants through metabolic engineering. Science 1998, 282:2098-2100.
97. Shintani D.K., Cheng Z., DellaPenna D. The role of 2-methyl-6-phytylbenzoquinone methyltransferase in determining tocopherol composition in Synechocystis sp. PCC6803. FEBS Lett. 2002, 511:1-5.
98. Sierla M., Rahikainen M., Salojärvi J., Kangasjärvi J., Kangasjärvi S. Apoplastic and chloroplastic redox signaling networks in plant stress responses. Antiox. Redox Signal. 2013, 18:2220-2239.
99. Sies H., Menck C.F. Singlet oxygen induced DNA damage. Mutat. Res. 1992, 275:367-375.
100. Stocker A., Rüttimann A., Woggon W.-D. Identification of the tocopherol cyclase in the blue-green algae Anabaena variabilis Kutzing (cyanobacteria). Helv. Chim. Acta 1993, 76:1729-1738.
101. Strzałka K., Szymanska R., Swiezewska E., Skorupinska-Tudek K., Suwalsky M. Tocochromanols, plastoquinone and polyprenols in selected plant species from Chilean Patagonia. Acta Biol. Crac. Bot. 2009, 51:39-44.
102. Strzałka K., Szymanska R., Suwalsky M. Prenyllipids and pigments content in selected Antarctic lichens and mosses. J. Chilean Chem. Soc. 2011, 56:808-811.
103. 6f complex as an indigenous photodynamic generator of singlet oxygen in thylakoid membranes. Photochem. Photobiol. 2000, 71:10-109.
104. Suzuki N., Koussevitzky S., Mittler R., Miller G. ROS and redox signalling in the response of plants to abiotic stress. Plant Cell Environ. 2012, 35:259-270.
105. Szymanska R., Kruk J. Tocopherol content and isomer's composition in selected plant species. Plant Physiol. Biochem. 2008, 46:29-33.
106. Szymanska R., Kruk J. γ-tocopherol dominates in young leaves of runner bean (Phaseolus coccineus) under a variety of growing conditions: the possible functions of γ-tocopherol. Phytochemistry 2008, 69:2142-2148.
107. Szymanska R., Kruk J. Plastoquinol is the main prenyllipid synthesized during acclimation to high-light conditions in Arabidopsis and converted to plastochromanol by tocopherol cyclase. Plant Cell Physiol. 2010, 51:537-545.
108. Szymanska R., Kruk J. Identification of hydroxy-plastochromanol in Arabidopis leaves. Acta Biochim. Pol. 2010, 57:105-107.
109. Szymanska R., Latowski D., Strzalka K. Chloroplasts and strong photoprotective mechanisms. Curr. Chem. Biol. 2012, 6:254-264.
110. 4 excess on lipoic acid and tocopherols in Genovese and Fine basil (Ocimum basilicum). Ann. Appl. Biol. 2013, 163:23-32.
111. Telfer A. What is β-carotene doing in the photosystem II reaction centre? Phil. Trans. R. Soc. Lond. B 2002, 357:1431-1440.
112. Torres M.A., Dangl J.L. Functions of the respiratory burst oxidase in biotic interactions, abiotic stress and development. Curr. Opin. Plant Biol. 2005, 8:397-403.
113. Trebst A. A specific role for tocopherol and of chemical singlet oxygen quenchers in the maintenance of photosystem II structure and function in Chlamydomonas reinhardii. FEBS Lett. 2002, 516:156-160.
114. Trebst A. Function of β-carotene and tocopherol in photosystem II. Z Naturforsch. C 2003, 58:609-620.
115. Trianthaphylides C., Krischke M., Hoeberichts A., Ksas B., Gresser G., Havaux M., et al. Singlet oxygen is a major reactive oxygen species involved in photooxidative damage in plants. Plant Physiol. 2008, 148:960-968.
116. Valentin H.E., Lincoln K., Moshiri F., Jensen P.K., Qi Q., Venkatesh T.V. The Arabidopsis vitamin E pathway gene 5-1 mutant reveals a critical role for phytol kinase in seed tocopherol biosynthesis. Plant Cell 2006, 18:212-224.
117. Vanderauwera S., Zimmermann P., Rombauts S., Vandenabeele S., Langebartels C., Gruissem W., et al. Genome-wide analysis of hydrogen peroxide-regulated gene expression in Arabidopsis reveals a high-light induced transcriptional cluster involved in anthocyanins biosynthesis. Plant Physiol. 2005, 139:806-821.
118. Vranova E., Inze D., van Breusegem F. Signal transduction during oxidative stress. J. Exp. Bot. 2002, 53:1227-1236.
119. Weber H. Fatty acid-derived signals in plants. Trend Plant Sci. 2002, 7:217-224.
120. White D.A., Fisk I.D., Gray D.A. Characterization of oat (Avena sativa L.) oil bodies and intrinsically associated E-vitamers. J. Cer. Sci. 2006, 43:244-249.
121. Zbierzak A.M., Kanwischer M., Wille C., Vidi P.A., Giavalisco P., Lohmann A., et al. Intersection of tocopherol and plastoquinol metabolic pathways at the plastoglobule. Biochem. J. 2010, 425:389-399.