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Oxidation of vacuolar and apoplastic phenolic substrates by peroxidase: Physiological significance of the oxidation reactions

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Abstract

Phenolic components and peroxidases are localized in vacuoles. Vacuolar peroxidase can oxidize phenolics when H2O2 is formed in vacuoles or tonoplasts, or when H2O2 formed outside of vacuoles is diffused into the organelles. In a mixture of phenolics containing a good and a poor substrate for peroxidase, a radical transfer reaction is possible from the radicals of the good substrate to the poor substrate, resulting in the enhancement of oxidation of the poor substrate. Phenoxyl radicals formed by peroxidase-dependent reactions are reduced by ascorbate in vacuoles. So, as long as ascorbate is present in vacuoles, the accumulation of oxidation products of phenolics is not significant. This suggests that ascorbate/phenolics/peroxidase systems in the vacuoles can scavenge H2O2. During aging, some phenolics are accumulated in vacuoles and the apoplast, and the accumulated phenolics are oxidized to brown components by peroxidase-dependent reactions. The brown components can produced O2 and H2O2 by autooxidation. The significance and the mechanisms of browning are discussed in tobacco leaves and onion scales.

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References

  • Albrecht C & Kohlenbach, HW(1990) L-DOPA content, peroxidase activity, and response to H 2 O 2 of Vicia faba L. and V. narboneensis L. in situ and in vitro. Protoplasma 154: 144–150.

    Google Scholar 

  • Amborabé B-E, Fleurat-Lessard P, Chollet J-F & Robin G (2002) Antifungal effects of salicylic acid and other benzoic acid deriv-atives towards Eutypa lata: structure-activity relationship. Plant Physiol. Biochem. 40: 1051–1061.

    Google Scholar 

  • Andrews J, Adams SR, Burton KS & Evered CE (2002) Subcellular localization of peroxidase in tomato fruit skin and the possible implication for the regulation of fruit growth. J. Exp. Bot. 53: 2185–2191.

    Google Scholar 

  • Asada K (1992) Ascorbate peroxidase - a hydrogen peroxide-scavenging enzyme in plants. Physiol. Plant. 85: 235–241.

    Google Scholar 

  • Asada K (1999) The water-water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annu. Rev. ]Plant Physiol. Plant Mol. Biol. 50: 601–639.

    Google Scholar 

  • Barz W, Köster J, Weltring K-M & Strack D (1985) Recent advances in the metabolism and degradation of phenolic compounds in plants and animals. Ann. Proc. Phytochem. Soc. Eur. 25: 307–347.

    Google Scholar 

  • Barz W & Welle R (1992) Biosynthesis and metabolism of isoflavones and pterocarpan phytoalexins in chickpea, soybean and phytophathogenic fungi. In: HA Stafford and RK Ibrahim (eds) Phenolic Metabolism in Plants (pp. 139–164), Plenum Press, New York.

    Google Scholar 

  • Bernal MA & Ros Barcelo A (1996) 5,5-Dicapsaicin, 4 -O-5-dicapsaicin ether, and dehydrogenation polymers with high molecular weights are the main products of the oxidation of capsaicin by peroxidase from hot pepper. J. Agric. Food Chem. 44: 3085–3089.

    Google Scholar 

  • Bernards MA, Fleming WD, Llewellyn DB, Priefer R, Yang X, Sabatino A & Plourde GL (1999) Biochemical characterization of the suberization-associated anionic peroxidase of potato. Plant Physiol. 121: 135–145.

    Google Scholar 

  • Bieza K & Lois R (2001) An Arabidopsis mutant tolerant to lethal ultraviolet-B levels shows constitutively elevated accumulation of flavonoids and other phenolics. Plant Physiol. 126: 1105–1115.

    Google Scholar 

  • Bors W, Heller W & Michel C (1997) The chemistry of flavonoids. In: CA Rice-Evans, CA and Packer L (eds), Flavonoids in Health and Disease (pp. 111–136), Marcel Dekker, New York.

    Google Scholar 

  • Brown DE, Rashotte AM, Murphy AS, Normanly J, Tague BW, Peer WA, Taiz L & Murday GK (2001) Flavonoids act as negative regulators of auxin transport in vivo in Arabidopsis. Plant Physiol. 126: 524–535.

    Google Scholar 

  • Cantos E, Tudela JA, Gil MI & Espín JC (2002) Phenolic compounds and related enzymes are not rate-limiting in browning development of fresh-cut potatoes. J. Agric. Food Chem. 50: 3015–3023.

    Google Scholar 

  • Canvin DT (1990) Photorespiration and CO 2-concentrating mechanism. In: Dennis DT and Turpin DH (eds), Plant Physiology, Biochemistry and Molecular Biology (pp. 253–273), Longman Scientific & Technical, Essex.

    Google Scholar 

  • Chio S-S, Hyde JS & Sealy RC (1982) Paramagnetism in melanins: pH dependence. Arch. Biochem. Biophys. 215: 100–106.

    Google Scholar 

  • Contreras-Padilla M & Yahia EM (1998) Changes in capsaicinoids during development, maturation, and senescence of chile peppers and relation with peroxidase activity. J. Agric Food Chem. 46: 2075–2079.

    Google Scholar 

  • Davin LB, Lewis NG & Umezawa T (1992) Phenylpropanoid metabolism: biosynthesis of monolignols, lignans and neolignans, lignins and suberins. In: Stafford HA and RK Ibrahim RK (eds), Phenolic Metabolism in Plants (pp. 325–375), Plenum Press, New York.

    Google Scholar 

  • Dixon RA & Paiva NL (1995) Stress-induced phenylpropanoid metabolism. Plant Cell 7: 1085–1097.

    Google Scholar 

  • Estrada B, Bernal MA, Díaz J, Pomar F & Merino F (2000) Fruit development in Capsicum annum: Changes in capsaicin, lignin, free phenolics, and peroxidase patterns. J. Agric. Food Chem. 48: 6234–6239.

    Google Scholar 

  • Fujiwake H, Suzuki T & Iwai K (1980) Intracellular localization of capsaicin and its analogues in Capsicum fruit II. The vacuolar as the intracellular accumulation site of capsaicinoid in the protoplast of Capsicum fruit. Plant Cell Physiol. 21: 1023–1030.

    Google Scholar 

  • Fukumoto LR, Toivonen PMA & Delaquis PJ (2002) Effects of wash water temperature and chlorination on phenolic metabolism and browning of stored iceberg lettuce photosynthetic and vascular tissues. J. Agric. Food Chem. 50: 4503–4511.

    Google Scholar 

  • Gális I, Simek P, Van Onckelen HA, Kakiuchi Y & Wabiko H (2002) Resistance of transgenic tobacco seedlings expressing the Agrobacterium tumefaciens C58-6b gene, to growth-inhibitory levels of cytokinin is associated with elevated IAA levels and activation of phenylpropanoid metabolism. Plant Cell Physiol. 43: 939–950.

    Google Scholar 

  • Giersch C (2000) Mathematical modelling of metabolism. Curr. Opin. Plant Biol 3: 249–253.

    Google Scholar 

  • Goodwin DC & Hertwig KM (2003) Peroxidase-catalyzed oxidation of capsaicinoids: Steady-state and transient-state kinetic studies. Arch. Biochem. Biophys. 417: 18–26.

    Google Scholar 

  • Grassmann J, Hippeli S & Elstner EF (2002) Plant's defense and its benefits for animals and medicine: role of phenolics and terpenoids in avoiding oxygen stress. Plant Physiol. Biochem. 40: 471–478.

    Google Scholar 

  • Grommeck R & Markakis P (1965) The effect of peroxidase on anthocyanin pigments. J. Food Sci. 29: 53–57.

    Google Scholar 

  • Halliwell B (1999) Food-derived antioxidants. Evaluating their importance in food and in vivo. Food Sci. Agric. Chem. 1: 67–109.

    Google Scholar 

  • Halliwell B & Gutteridge JMC (1999) Free Radicals in Biology and Medicine. Oxford University Press, Oxford.

    Google Scholar 

  • Halliwell B, Zhao K & Whiteman M (2000) The gastrointestinal tract: A major site of antioxidant action? Free Radic. Res. 33: 819–830.

    Google Scholar 

  • Heber U, Miyake C, Mano J, Ohno C & Asada K (1996) Monode-hydroascorbate radical detected by electron spin magnetic reson-ance spectrometry is a sensitive probe of oxidative stress in intact leaves. Plant Cell Physiol 37: 1066–1072.

    Google Scholar 

  • Hertog MGL & Katan MB (1997) Quercetin in foods, cardiovascular disease and cancer. In: Rice-Evans CA and Packer L (eds), Flavonoids in Health and Disease (pp. 447–467), Marcel Dekker, New York.

    Google Scholar 

  • Hirota S, Shimoda T & Takahama U (1998) Tissue and spatial distribution of flavonol and peroxidase in onion bulbs and stability of flavonol glucosides during boiling of the scales. J. Agric. Food Chem. 46: 3497–3502.

    Google Scholar 

  • Hirota S, Shimoda T & Takahama U (1999) Distribution of flavonols and enzymes participating in the metabolism in onion bulbs: mechanism of accumulation of quercetin and its glucosides in the abaxial epidermis. Food Sci. Technol. Res. 5: 384–387.

    Google Scholar 

  • Hirota S, Takahama U, Ansai T & Yoshitama K (2002) Oxidation of quercetin by salivary components II. Effects of quercetin on reactive oxygen metabolism by salivary polymorphonuclear leukocytes. Food Sci. Technol. Res. 8: 276–280.

    Google Scholar 

  • Horemans N, Asard H & Caubergs J (1994) The role of ascorbic acid free radical as an electron acceptor to cytochrome b-mediated trans-plasma membrane electron transport in higher plants. Plant Physiol. 104: 1455–1458.

    Google Scholar 

  • Horemans N, Asard H & Caubergs J (1997) The ascorbate carrier of higher plant plasma membranes preferentially translocate the fully oxidized (dehydroascorbate) molecule. Plant Physiol. 114: 1247–1253.

    Google Scholar 

  • Housti F, Andary C, Gargadennec A & Amssa M (2002) Effects of wounding and salicylic acid on hydroxycinnamic acids in Thunbergia alata. Plant Physiol. Biochem. 40: 761–769.

    Google Scholar 

  • Ishikawa T, Yoshimura K, Sakai K, Tamoi M, Takeda T & Shigeoka S (1998) Molecular characterization and physiological role of a glyoxysome-bound ascorbate peroxidase from spinach. Plant Cell Physiol. 39: 23–34.

    Google Scholar 

  • Jan C-Y, Takahama U & Kimura M (1991) Inhibition of photooxidation of á-tocopherol by quercetin in human blood cell membranes in the presence of hematoporphyrin as a photosensitizer. Biochim. Biophys. Acta 1086: 7–14.

    Google Scholar 

  • Jansen MAK, van den Noort RE, Tan MYA, Prinsen E, Lagrimini LM & Thorneley RNF (2001) Phenol-oxidizing peroxidases con-tribute to the protection of plants from ultraviolet radiation stress. Plant Physiol. 126: 1012–1023.

    Google Scholar 

  • Jiménez M. & Garcia-Carmona F (1999) Oxidation of the flavonol quercetin by polyphenol oxidase. J. Agric. Food Chem. 47: 56–60.

    Google Scholar 

  • Jovanovic SV, Steenken S, Simic MG & Hara Y (1997) Antioxidant properties of flavonoids: reduction potentials and electron transfer reactions of flavonoid radicals. In: CA Rice-Evans, CA and Packer L (eds), Flavonoids in Health and Disease (pp. 137–161), Marcel Dekker, New York.

    Google Scholar 

  • Kono Y, Kobayashi K, Tagawa S, Adachi K, Ueda A, Sawa Y & Shibata H (1997) Antioxidant activity of polyphenolics in diets. rate constants of reactions of chlorogenic acid and caffeic acid with reactive species of oxygen and nitrogen. Biochim. Biophys. Acta 1335: 335–342.

    Google Scholar 

  • Lamb C & Dixon RA (1997) The oxidative burst in plant disease resistance. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48: 251–275.

    Google Scholar 

  • Laukkanen H, Haggman H, Kontunen-Soppela S & Hohtola A (1999) Tissue browning of in vitro culture of Scots pine: role of peroxidase and polyphenol oxidase. Physiol. Plant. 106: 337–343.

    Google Scholar 

  • Long LH, Lan ANB, Hsuan FTY & Halliwell B (1999) Generation of hydrogen peroxide by 'antioxidant' beverages and the effect of milk addition. In cocoa the best beverage? Free Radic. Res. 31: 67–71.

    Google Scholar 

  • Marfak A, Trouillas P, Allais D-P, Champavier, Y, Calliste, C-A & Duroux J-L (2002) Radiolysis of quercetin in methanol solu-tion: Observation of depside formation. J. Agric Food Chem. 50: 4827–4833.

    Google Scholar 

  • Matsuda F, Morino K, Miyashita M & Miyagawa H (2003) Metabolic flux analysis of the phenylpropanoid pathway in wound-healing potato tuber tissueusing stable isotope-labeled tracer and LC-MS. Plant Cell Physiol. 44: 510–517.

    Google Scholar 

  • McDougall GJ (1991) Cell wall-associated peroxidases and lignification during growth of flax fibers. J. Plant Physiol. 139: 182–186.

    Google Scholar 

  • McDougall GJ (1992) Changes in cell wall-associated peroxidases during the lignification of flax fibers. Phytochemistry 31: 3385–3389.

    Google Scholar 

  • Mehdy MC, Sharma YK, Sathasivan K & Bays NW (1996) The role of activated oxygen species in plant disease resistance. Physiol. Plant. 98: 365–374.

    Google Scholar 

  • Mehlhorn H, Lelandais M, Korth HG & Foyer CH (1996) Ascorbate is the natural substrate for plant peroxidases. FEBS Lett. 378: 203–206.

    Google Scholar 

  • Niyogi KK (1999) Photoprotection revised: genetic and molecular approaches. Annu. Rev. Plant Physiol. Plant Mol. Biol. 50: 333–359.

    Google Scholar 

  • Noctor G & Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu. Rev. Plant Physiol. Plant Mol. Biol. 49: 249–279.

    Google Scholar 

  • Ogawa K, Kanematsu S & Asada K (1996) Intra-and extra-cellular localization of 'cytosolic' CuZn-superoxide dismutase in spinach leaf and hypocotyl. Plant Cell Physiol. 37: 790–799.

    Google Scholar 

  • Oldreive C. & Rice-Evans C (2001) The mechanisms for nitration and nitrotyrosine formation in vitro and in vivo: Impact of diet. Free Radic. Res. 35: 215–231.

    Google Scholar 

  • Olsson LC, Veit M & Bornman JF (1999) Epidermal transmittance and phenolic composition in leaves of atrazine-tolerant and atrazin-sensitive cultivars of Brassica napus grown under enhanced UV-B radiation. Physiol. Plant. 107: 259–266.

    Google Scholar 

  • Otter T & Polle A (1994) The influence of apoplastic ascorbate on the activities of cell-wall associated peroxidase and NADH oxidase in needles of Norway spruce (Picea abies L.). Plant Cell Physiol. 35: 1231–1238.

    Google Scholar 

  • Otter T & Polle A (1997) Characterization of acidic and basic apoplastic peroxidase form needles of Norway spruce (Picea abies L., Karrsten) with respect to lignifying substrates. Plant Cell Physiol. 38: 595–602.

    Google Scholar 

  • Pedreño MA, Bernal MA, Calderon AA, Ferrer MA, Lopez-Serrano M, Merino de Caceres F, Muñoz R & Ros Barceló A (1993) A general pattern for peroxidase isoenzyme localization and function in Vitaceae, Solanaceae and Leguminoseae. In: Welinder, KG, Rasmussen, SK Penel, C & Greppin H (eds), Plant Peroxidases. Biochemistry and Physiology (pp. 307–314), Rochat-Baumann, Inprimerie Nationale, Geneva.

    Google Scholar 

  • Pedreño MA, Ferrer MA, Gaspar Th, Muñoz R & Ros Barceló A (1995) The polyfunctionality of cell wall peroxidases avoids the necessity of an independent H 2 O 2-generating system for phenolic coupling in the cell wall. Plant Peroxidase Newslett. 5: 3–8.

    Google Scholar 

  • Peer WA, Brown DE, Tague BW, Muday GK, Taiz L & Murphy AS (2001) Flavonoid accumulation patterns of transparent testa mutants of Arabidopsis. Plant Physiol. 126: 536–548.

    Google Scholar 

  • Phillips DA (1992) Flavonoids: plant signals to soil microbes. In: Stafford HA and RK Ibrahim RK (eds), Phenolic Metabolism in Plants (pp 201–231), Plenum Press, New York.

    Google Scholar 

  • Rautenkranz, AAF, Li L, Machler F, Martinoia E & Oertli JJ (1994) Transport of ascorbic acid and dehydroascorbic acid across protoplast and vacuolar membranes isolated from barley (Hordeum vulgare L. cv. Gerbel.). Plant Physiol. 106: 187–193.

    Google Scholar 

  • Reichling J (1999) Plant-microbe interactions and secondary metabolites with antiviral, antibacterial and antifungal properties. In: Wink M (ed.), Functions of Plant Secondary Metabolites and their Exploitation in Biotechnology (pp. 187–273), Sheffield Academy Press, Sheffield.

    Google Scholar 

  • Rice-Evans CA & Packer L <nt >(eds) </nt > (1998) Flavonoids in Health and Disease. Marcel Dekker, New York.

    Google Scholar 

  • Ros Barceló A, Ferrer MA, Garcia-Florenciano E & Muñoz R (1991) The tonoplast localization of two basic isoperoxidases of high pI in Lupinus. Bot. Acta 104: 272–278.

    Google Scholar 

  • Rozema J, van der Staaij J, Björn LO & Caldwell M (1997) UV-B as an environmental factor in the plant life: Stress and regulation. Trends Ecol. Evol. 12: 22–28.

    Google Scholar 

  • Sánchez M, Queijeiro E, Revilla G & Zarra I (1997) Changes in ascorbate levels in apoplastic fluid during growth of pine hypo-cotyls. Effect on peroxidase activities associated with cell walls. Physiol. Plant. 101: 815–820.

    Google Scholar 

  • Sato Y, Sugiyama M, Gorecki RJ, Fukuda H & Komamine A (1993) Interrelationship between lignin deposition and the activities of peroxidase isozymes in differentiating tracheary elements of Zinnia. Planta 189: 584–589.

    Google Scholar 

  • Schreier P & Miller E (1985) Studies on flavonol degradation by peroxidase (donor: H 2 O 2-oxidoreductase, EC 1.11.1.7): Part 2-quercetin. Food Chem. 18: 301–317.

    Google Scholar 

  • Sealy RC, Felix CC, Hyde JS & Swartz HM (1980) Structure and reactivity of melanins: Influence of free radicals and metal ions. In: Pryor WA (ed), Free Radicals in Biology, Vol. 4 (pp. 209- 259), Academic Press, London.

    Google Scholar 

  • Solecka D, Boudet AM & Kacperska A (1999) Phenylpropanoid and anthocyanin changes in low temperature treated winter oilseed rape leaves. Plant Physiol. Biochem. 33: 585–591.

    Google Scholar 

  • Stefanowska M, Kuras M & Kacperska A (2002) Low temperature-induced modifications in cell ultrastructure and localization of phenolics in winter oilseed rape (Brassica napus L. var. oleifera L.) leaves. Ann. Bot. 90: 637–645.

    Google Scholar 

  • Takahama U (1986) Spectrophotometric study on the oxidation of rutin by horseradish peroxidase and characteristics of the oxidation products. Biochim. Biophys. Acta 882: 445–451.

    Google Scholar 

  • Takahama U (1987) Oxidation products of kaempferol by superoxide anion radical. Plant Cell Physiol. 28: 953–957.

    Google Scholar 

  • Takahama U (1988) Oxidation of flavonols by hydrogen peroxide in epidermal and guard cells of Vicia faba L. Plant Cell Physiol. 29: 433–438.

    Google Scholar 

  • Takahama U (1992) Hydrogen peroxide scavenging systems in vacuoles of mesophyll cells of Vicia faba. Phytochemistry 31: 1127–1133.

    Google Scholar 

  • Takahama U (1993) Regulation of peroxidase-dependent oxidation of phenolics by ascorbic acid: different effects of ascorbic acid on the oxidation of coniferyl alcohol by the apoplastic soluble and cell wall-bound peroxidases from epicotyls of Vigna angularis. Plant Cell Physiol. 34: 809–817.

    Google Scholar 

  • Takahama U (1995) Oxidation of hydroxycinnamic acid and hydroxycinnamyl alcohol derivatives by laccase and peroxidase. Interactions among p-hydroxyphenyl, guaiacyl and syringyl groups during the oxidation reactions. Physiol. Plant. 93: 61–68.

    Google Scholar 

  • Takahama U & Egashira T (1991) Peroxidases in vacuoles of Vici a faba leaves. Phytochemistry 30: 73–77.

    Google Scholar 

  • Takahama U & Hirota S (2000) Transformation of quercetin glucosides to the aglycone and formation of antifungal agents by peroxidase-dependent oxidationof quercetin on browning of onion scales. Plant Cell Physiol. 41: 1021–1029.

    Google Scholar 

  • Takahama U, Hirotsu M & Oniki T (1999) Age-dependent changes in levels of ascorbic acid and chlorogenic acid, and activities of peroxidase and superoxide dismutase in the apoplast of tobacco leaves: Mechanism of the oxidation of chlorogenic acid in the apoplast. Plant Cell Physiol 40: 716–724.

    Google Scholar 

  • Takahama U & Oniki T (1991) Participation of peroxidase in the metabolism of 3,4-dihydroxyphenylalanine and hydrogen per-oxide in vacuoles of Vicia faba L. mesophyll cells. Plant Cell Physiol. 32: 745–754.

    Google Scholar 

  • Takahama U & Oniki T (1992) Regulation of peroxidase-dependent oxidation of phenolics in the apoplast of spinach leaves by ascorbate. Plant Cell Physiol. 33: 379–387.

    Google Scholar 

  • Takahama U & Oniki T (1997a) A peroxidase/phenolics/ascorbate system can scavenge hydrogen peroxide in plant cells. Physiol. Plant. 101: 845–852.

    Google Scholar 

  • Takahama U & Oniki T (1997b) Enhancement of peroxidase-dependent oxidation of sinapyl alcohol by an apoplastic component, 4-coumaric acid ester isolated from epicotyls of Vigna angularis L. Plant Cell Physiol. 38: 456–462.

    Google Scholar 

  • Takahama U & Oniki T (1998) 3,4-Dihydroxyphenylalanine is oxidized by phenoxyl radicals of hydroxycinnamic acid esters in leaves of Vicia faba L. J. Plant Res. 111: 487–494.

    Google Scholar 

  • Takahama U, Oniki T & Shimokawa H (1996) A possible mechanism for the oxidation of sinapyl alcohol by peroxidase-dependent reactions in the apoplast: enhancement of the oxidation by hydroxycinnamic acid and components of the apoplast. Plant Cell Physiol. 37: 499–504.

    Google Scholar 

  • Takahama U, Oniki T & Hirota S (2001) Phenolic components of brown scales of onion bulbs produce hydrogen peroxide by autooxidation. J. Plant Res. 114: 395–402.

    Google Scholar 

  • Takahashi A, Takeda K & Ohnishi T (1991) Light-induced anthocyanin reduces the extent of damage to DNA in UV-irradiated Centaurea cyanus cells in culture. Plant Cell Physiol. 32: 541–547.

    Google Scholar 

  • Thomas LT & Jen JJ (1980) The cytochemical localization of peroxidase in tomato fruit cells. J. Food Biochem. 4: 247–259.

    Google Scholar 

  • Tsushida T & Suzuki M (1995) Content of flavonol glucosides and some properties of enzymes metabolizing the glucosides in onion. Nippon Shokuhin Kogyo Gakkaishi 43: 642–649.

    Google Scholar 

  • Veljovic-Jovanovic S, Oniki T & Takahama U (1998) Detection of monodehydroascorbic acid radical in sulfitetreated leaves and mechanism of its formation. Plant Cell Physiol. 39: 1203–1208.

    Google Scholar 

  • Walker JC & Stahmann MA (1955) Chemical nature of disease resistance in plants. Annu. Rev. Plant Physiol. 6: 351–366.

    Google Scholar 

  • Welinder KG & Gajhede M. (1993) Structure and evolution of peroxidase. In: Welinder KG, Rasmussen SK, Penel C & Greppin H (eds), Plant Peroxidases. Biochemistry and Physiology (pp. 35–42), Rochat-Baumann, Imprimerie Nationale, Geneva.

    Google Scholar 

  • Winkel-Shirley B (2001) Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology. Plant Physiol. 126: 485–493.

    Google Scholar 

  • Wu J and Lin L (2002) Ultrasound-induced stress responses of Panax ginseng cells: Enzymatic browning and phenolics production. Biotechnol. Prog. 18: 862–866.

    Google Scholar 

  • Yamasaki H & Grace S (1998) EPR detection of phytophenoxyl radicals by zinc ions: evidence for the redox-coupling of plant phenolics with ascorbate in the H 2 O 2-peroxidase system. FEBS Lett. 422: 377–380.

    Google Scholar 

  • Yamasaki H, Sakihama Y & Ikehara N (1997) Flavonoid-peroxidase reaction as a detoxification mechanism of plant cells against H 2 O 2. Plant Physiol. 115: 1405–1412.

    Google Scholar 

  • Yamasaki H, Uefuji H & Sakihama Y (1996) Bleaching of the red anthocyanin induced by superoxide. Arch. Biochem. Biophys. 332: 183–186.

    Google Scholar 

  • Yamaguchi K, Mori H & Nishimura M (1995) A novel isoenzymes of ascorbate peroxidase localized on glyoxysomal and leaf peroxisomal membranes in pumpkin. Plant Cell Physiol. 36: 1157–1162.

    Google Scholar 

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Takahama, U. Oxidation of vacuolar and apoplastic phenolic substrates by peroxidase: Physiological significance of the oxidation reactions. Phytochemistry Reviews 3, 207–219 (2004). https://doi.org/10.1023/B:PHYT.0000047805.08470.e3

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