Abstract
Recent studies have revealed that dietary flavonoids are potent radical scavengers, acting in a manner similar to ascorbate and [alpha]-tocopherol. However, it is still not clear whether flavonoids have a similar antioxidative function in plants. We examined the possibility that flavonoids could function as stress protectants in plant cells by scavenging H2O2. Two major flavonoids, quercetin and kaempferol glycosides, were isolated from leaves of the tropical tree Schefflera arboricola Hayata. Both glycosides and aglycones of isolated flavonols were oxidized by H2O2 in the presence of horse-radish peroxidase and/or in a soluble fraction of S. arboricola leaf extract. The rates of oxidation were in the order quercetin > kaempferol > quercetin glycoside >> kaempferol glycoside. Judging from the effects of inhibitors such as KCN, p-chloromercuribenzoate, and 3-amino-1H-1,2,4-triazole, we conclude that guaiacol peroxidase in the soluble fraction catalyzes H2O2-dependent oxidation of flavonols. In the flavonol-guaiacol peroxidase reaction, ascorbate had the potential to regenerate flavonols by reducing the oxidized product. These results provide further evidence that the flavonoid-peroxidase reaction can function as a mechanism for H2O2 scavenging in plants.
Full Text
The Full Text of this article is available as a PDF (1.3 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bors W., Heller W., Michel C., Saran M. Flavonoids as antioxidants: determination of radical-scavenging efficiencies. Methods Enzymol. 1990;186:343–355. doi: 10.1016/0076-6879(90)86128-i. [DOI] [PubMed] [Google Scholar]
- Bors W., Michel C., Saran M. Flavonoid antioxidants: rate constants for reactions with oxygen radicals. Methods Enzymol. 1994;234:420–429. doi: 10.1016/0076-6879(94)34112-5. [DOI] [PubMed] [Google Scholar]
- Castelluccio C., Paganga G., Melikian N., Bolwell G. P., Pridham J., Sampson J., Rice-Evans C. Antioxidant potential of intermediates in phenylpropanoid metabolism in higher plants. FEBS Lett. 1995 Jul 10;368(1):188–192. doi: 10.1016/0014-5793(95)00639-q. [DOI] [PubMed] [Google Scholar]
- Conklin P. L., Williams E. H., Last R. L. Environmental stress sensitivity of an ascorbic acid-deficient Arabidopsis mutant. Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9970–9974. doi: 10.1073/pnas.93.18.9970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dixon R. A., Paiva N. L. Stress-Induced Phenylpropanoid Metabolism. Plant Cell. 1995 Jul;7(7):1085–1097. doi: 10.1105/tpc.7.7.1085. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grace S. C., Logan B. A. Acclimation of Foliar Antioxidant Systems to Growth Irradiance in Three Broad-Leaved Evergreen Species. Plant Physiol. 1996 Dec;112(4):1631–1640. doi: 10.1104/pp.112.4.1631. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hrazdina G., Marx G. A., Hoch H. C. Distribution of Secondary Plant Metabolites and Their Biosynthetic Enzymes in Pea (Pisum sativum L.) Leaves : Anthocyanins and Flavonol Glycosides. Plant Physiol. 1982 Sep;70(3):745–748. doi: 10.1104/pp.70.3.745. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jan C. Y., Takahama U., Kimura M. Inhibition of photooxidation of alpha-tocopherol by quercetin in human blood cell membranes in the presence of hematoporphyrin as a photosensitizer. Biochim Biophys Acta. 1991 Oct 15;1086(1):7–14. doi: 10.1016/0005-2760(91)90148-b. [DOI] [PubMed] [Google Scholar]
- Landry L. G., Chapple C. C., Last R. L. Arabidopsis mutants lacking phenolic sunscreens exhibit enhanced ultraviolet-B injury and oxidative damage. Plant Physiol. 1995 Dec;109(4):1159–1166. doi: 10.1104/pp.109.4.1159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mount D. W. DNA repair. Reprogramming transcription. Nature. 1996 Oct 31;383(6603):763–764. doi: 10.1038/383763a0. [DOI] [PubMed] [Google Scholar]
