References
- Hu SY. A contribution to our knowledge of ginseng. Am J Chin Med 1977;5:1-23. https://doi.org/10.1142/S0192415X77000026
- Baranov A. Recent advances in our knowledge of the morphology, cultivation and uses of ginseng (Panax ginseng C.A. Meyer). Econ Bot 1966;20:403-6. https://doi.org/10.1007/BF02904062
- Evans BL. Ginseng: root of ChineseeCanadian relations. Can Hist Rev 1985;66:1-26. https://doi.org/10.3138/CHR-066-01-01
- Wang YQ. A preliminary study on cause of ginseng red skin disease in the second ginseng farm of Jinyu county. Spec Wild Econ Anim Plant Res 1963;2:9-15 [in Chinese].
- Zhang YC, Wang ZS, Li JF, Gao KJ, Sun SJ, Wang YL. An investigation of cause and protective method of ginseng red skin disease. Spec Wild Econ Anim Plant Res 1984;1:21-4 [in Chinese].
- Wu KY. The relationship between ginseng red skin disease and inorganic ions. Chin Trad Med 1989;12:13-4 [in Chinese].
- Zhao YF. The progress of diagnosis and comprehensive control of ginseng red skin disease. Spec Wild Econ Anim Plant Res 1998;1:41-6 [in Chinese].
- Li ZH, Tian SZ, Sun YJ, Guo SY, Liu ZR. The relationship between ginseng red skin root disease and soil ecology conditions. Ecol J 1999;19:864-9 [in Chinese].
- Liu X, Yang ZM, Gao LL, Xiang WY, Zhang B, Xie ZL, You JF. Comparison of the characteristics of artificial ginseng bed soils in relation to the incidence of ginseng red skin disease. Exp Agric 2014;50:59-71. https://doi.org/10.1017/S0014479713000367
- Parke JL. Shot well KM. Diseases of cultivated ginseng. Univ Wisconsin Madison Coll Agric Life Sci Res Bull 1989;3465:16.
- Campeau CA. Effects of ethephon on floral abscission and root quality of North American ginseng (Panax quinquefolius L.). MS dissertation. Ontario, Canada: University of Guelph; 2002.
- Campeau CA, Proctor JTA, Jackson CJC, Rupasinghe HPV. Rust-spotted north American ginseng roots: phenolic, antioxidant, ginsenoside and mineral nutrient. Hort Sci 2003;38:179-82.
- Rahman M, Punja ZK. Biochemistry of ginseng root tissues affected by rusty root symptoms. Plant Physiol Biochem 2005;43:1103-14. https://doi.org/10.1016/j.plaphy.2005.09.004
- Dixon RA, Paiva NL. Stress-induced phenyl propanoid metabolism. Plant Cell 1995;7:1805-97.
- Heidarabadi MD, Ghanati F, Fujiwara T. Interaction between boron and aluminum and their effects on phenolic metabolism of Linum usitatissimum L. roots. Plant Physiol Biochem 2011;49:1377-83. https://doi.org/10.1016/j.plaphy.2011.09.008
- Ofei-Manu P, Wagatsuma T, Ishikawa S, Tawaraya K. The plasma membrane strength of the root-tip cells and root phenolic compounds are correlated with Al tolerance in several common woody plants. Soil Sci Plant Nutr 2001;47:359-76. https://doi.org/10.1080/00380768.2001.10408399
- Kidd PS, Lugany M, Poschenreder C, Gunse B, Barcelo J. The role of root exudates in aluminium resistance and silicon-induced amelioration of aluminium toxicity in three varieties of maize (Zea may L.). J Exp Bot 2001;52:1339-52.
- Horemas N, Foyer CH, Asard H. Transport and action of ascorbate at the plasma membrane. Trends in Plant Sci 2000;5:263-7. https://doi.org/10.1016/S1360-1385(00)01649-6
- Pignocchi C, Foyer CH. Apoplastic ascorbate metabolism and its role in the regulation of cell signaling. Curr Opin Plant Biol 2003;6:379-89. https://doi.org/10.1016/S1369-5266(03)00069-4
- Dipierro N, Mondelli D, Paciolla C, Brunetti G, Dipierro S. Changes in the ascorbate system in the response of pumpkin (Cucurbita pepo L.) roots to aluminum stress. J Plant Physiol 2005;162:529-36. https://doi.org/10.1016/j.jplph.2004.06.008
- Koukol J, Conn EE. The metabolism of aromatic compounds in higher plants, purification and properties of the phenylalanine deaminase of Herdeum vulagare. J Biol Chem 1961;236:2690-8.
- Anderson JV, Morris CF. An improved whole seed assay for screening wheat germplasm for polyphenol oxidase activity. Crop Sci 2001;41:1697-705. https://doi.org/10.2135/cropsci2001.1697
- Hodges DM, Delong JM, Forney CF. Improving the thiobarbituric acid reactive substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 1999;207:604-11. https://doi.org/10.1007/s004250050524
- Patterson BD, MacRae EA, Ferquson IB. Estimation of hydrogen peroxide in plant extracts using titanium (IV). Anal Biochem 1984;139:487-92. https://doi.org/10.1016/0003-2697(84)90039-3
- Able AJ, Guest DI, Sutherland MW. Use of a new tetrazolium-based assay to study the production of superoxide radicals by tobacco cell cultures challenged with avirulent zoospores of Phytophthora parasitica var nicotinae. Plant Physiol 1998;117:491-9. https://doi.org/10.1104/pp.117.2.491
- Castillo FI, Penel I, Greppin H. Peroxidase release induced by ozone in Swdum album leaves. Plant Physiol 1984;74:846-51. https://doi.org/10.1104/pp.74.4.846
- Asada K. Chloroplasts: formation of active oxygen and its scavenging. Methods Enzymol 1984;105:422-9.
- Dhindsa RS, Plumb-Dhindsa P, Throne TA. Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation and decreased levels of superoxide dismutase and catalase. J Exp Bot 1981;32:93-101. https://doi.org/10.1093/jxb/32.1.93
- Hossain MA, Nakano Y, Asada K. Monodehydroascorbate reductase in spinach chloroplasts and its participation in the regeneration of ascorbate for scavenging hydrogen peroxide. Plant Cell Physiol 1984;25:385-95.
- Foyer CH, Halliwell B. The presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta 1976;133:21-5. https://doi.org/10.1007/BF00386001
- Griffith OW. Determination of glutathione and glutathione disulphide using glutathione reductase and 2-vinypyridine. Anal Biochem 1980;106:207-12. https://doi.org/10.1016/0003-2697(80)90139-6
- Gatzek S, Wheeler GL, Smirnoff N. Antisense suppression of l-galactose dehydrogenase in Arabidopsis thaliana provides evidence for its role in ascorbate synthesis and reveals light modulated l-galactose synthesis. Plant J 2002;30:541-53. https://doi.org/10.1046/j.1365-313X.2002.01315.x
- Hodges D, Andrews C, Johnson D, Hamilton R. Antioxidant compound response to chilling stress in differentially sensitive inbred maize 23 lines. Physicol Plant 1996;98:685-92. https://doi.org/10.1111/j.1399-3054.1996.tb06672.x
- Zhang XB, Liu CJ. Multifaceted regulations of gateway enzyme phenylalanine Ammonia-lyase in the biosynthesis of phenylpropanoids. Mol Plant 2015;8:17-27. https://doi.org/10.1016/j.molp.2014.11.001
- Pourcel L, Routaboul JM, Cheynier V, Lepiniec L, Debeaujon I. Flavonoid oxidation in plants: from biochemical properties to physiological functions. Trends Plant Sci 2006;12:29-36.
- Marusck CM, Trobough NM, Flurkey WH, Inlow JK. Comparative analysis of polyphenol oxidase from plant and fungal species. J Inorg Chem 2006;100:108-23.
-
Asada K. The role of ascorbate peroxidase and monodehydroascorbate reducases in
$H_2O_2$ scavenging in plants. In: Scandalions JG, editor. Oxidative stress and the molecular biology of antioxidant defenses. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 1987. p. 715-35. - Noctor G, Foyer CH. Ascorbic and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 1998;49:249-79. https://doi.org/10.1146/annurev.arplant.49.1.249
- Richards KD, Schott EJ, Sharma YK, Davis KR, Gardner RC. Aluminum induces oxidative stress genes in Arabidopsis thaliana. Plant Physiol 1998;116:409-18. https://doi.org/10.1104/pp.116.1.409
- Sakihama Y, Yamasaki H. Lipid peroxidation induced by phenolics in conjunction with aluminum ions. Biol Plant 2002;45:249-54. https://doi.org/10.1023/A:1015152908241
- Vermerris W, Nicholson R. Phenolic compound biochemistry (Chapter 2). Chemical properties of phenolic compounds. e-ISBN: 978-1-4020-5164-7. 2009p.43. Spinger.com.
- Ayala-Silva T, Al-Hamadani S. Interactive effects of polyactic acid with different aluminum concentrations on growth, pigment concentrations, and carbohydrate accumulation of Azolla. Am Fern J 1997;87:120-6. https://doi.org/10.2307/1547833
- Yang DC, Kim YH, Yun KY, Lee SS, Kwon JN, Kang HM. Red-colored phenomena of ginseng (Panax ginseng C. A. Meyer): root and soil environment. J Ginseng Sci 1997;21:91-7.
- Wang YP, Li ZH, Sun YJ, Guo SW, Tian SZ, Liu ZR. Studies on the genesis of ginseng rust spots. Korean J Ginseng Sci 1997;21:69-77.
- You JF, Liu X, Zhang B, Xie ZL, Hou ZG, Yang ZM. Seasonal changes in soil acidity and related properties in ginseng artificial bed soils under a plastic shade. J Ginseng Res 2015;39:81-8. https://doi.org/10.1016/j.jgr.2014.08.002
- Wissemeier AH, Horst WJ. Effect of light intensity on manganese toxicity symptoms and callose formation in cowpea (Vigna unguiculata (L.) Walp.). Plant Soil 1992;143:299-309. https://doi.org/10.1007/BF00007886
- Appel HM. Phenolics in ecological interactions: the importance of oxidation. J Chem Ecol 1993;9:1521-52.
- Takahama U. Redox state of ascorbic acid in the apoplast of stems of Kalanchoe daigremontiana. Physiol Plant 1993;89:791-8. https://doi.org/10.1111/j.1399-3054.1993.tb05286.x
- Takahama U, Oniki T. Regulation of peroxidase-dependent oxidation of phenolics in the apoplast of spinach leaves by ascorbate. Plant Cell Physiol 1992;33:379-87.
- Sakihama Y, Cohen MF, Grace SC. Plant phenolic antioxidant and prooxidant activities: phenolics-induced oxidative damage mediated by metals in plants. Toxicology 2002;177:67-80. https://doi.org/10.1016/S0300-483X(02)00196-8
- Kalyanaraman B. Characterization of O-semiquinoe radicals in biological systems. Methods Enzymol 1990;186:333-43.
- Sanchez M, Queijeiro E, Revilla G, Zarra I. Changes in ascorbate levels in apoplastic fluid during growth of pine hypocotyls. Effect on peroxides activities associated with cell walls. Physiol Plant 1997;101:815-20. https://doi.org/10.1111/j.1399-3054.1997.tb01068.x
- Isaacs NS, van Eldik R. A mechanistic study of the reduction of quinines by ascorbic acid. J Chem Soc Dalton Trans 1997;2:1465-8.
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