2003
DOI: 10.1271/bbb.67.1443
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New Potent Antioxidative Hydroxyflavanones Produced withAspergillus saitoifrom Flavanone Glycoside in Citrus Fruit

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Cited by 57 publications
(42 citation statements)
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“…13,14) Furthermore, the production of the potent antioxidant, 8-hydroxyhesperetin, by the fermentation of hesperidin (hesperetin 7-O--rutinoside) with A. saitoi has been reported. 23) The filamentous fungus of A. saitoi of used in fermented foods has been shown to have the capability for hydrolysis to the aglycone from a flavonoid glycoside and for hydroxylation to o-dihydroxyflavonoid. 21,22) The koji made by the fermentation of soybeans with A. awamori reportedly has high antioxidative activity, although the antioxidants linked to this activity are not clear.…”
Section: Resultsmentioning
confidence: 99%
“…13,14) Furthermore, the production of the potent antioxidant, 8-hydroxyhesperetin, by the fermentation of hesperidin (hesperetin 7-O--rutinoside) with A. saitoi has been reported. 23) The filamentous fungus of A. saitoi of used in fermented foods has been shown to have the capability for hydrolysis to the aglycone from a flavonoid glycoside and for hydroxylation to o-dihydroxyflavonoid. 21,22) The koji made by the fermentation of soybeans with A. awamori reportedly has high antioxidative activity, although the antioxidants linked to this activity are not clear.…”
Section: Resultsmentioning
confidence: 99%
“…Based on experimentation with free-radical scavenging system 1, 1-diphenyl-2-picrylhydrazyl and the methyl linoleate oxidation system, fermentation produced hydroxyflavone forms (8-hydroxyhesperitin, 6-hydroxynaringenin, and 8-hydroxynaringenin) are more potent free-radical scavengers with greater antioxidant activity than the aglycones hesperitin and naringenin. Aglycone derivatives are, however, more successful antioxidants than flavonone glycosides hesperidin and naringin (81).…”
Section: Orange Pulp Components and Their Effectsmentioning
confidence: 99%
“…In this regard, it is noteworthy that other researchers have focused on the significant hypolipidaemic effects exhibited by hesperidin, a result that may be also correlated to its antioxidant capacity, as has been proposed (Fraga et al, 1987;Lonchampt et al, 1989;Monforte et al, 1995). Surprisingly, however, other researchers have reported that neither naringin nor hesperidin has antioxidative activity (Chen et al, 1990;Wang and Zheng, 1992), while others have supported the notion that both of these substances are weak antioxidants (Miyake et al, 2003). This controversy might be attributed either to the material itself and its purity, since it has been derived from different parts of the world along with the subsequent processing used for the extraction, or to the method applied to assess the antioxidant potential of these substances.…”
Section: Introductionmentioning
confidence: 98%