CHVÁTALOVÁ, Kateřina, Iva SLANINOVÁ, Lenka BŘEZINOVÁ and Jiří SLANINA. Influence of dietary phenolic acids on redox status of iron: Ferrous iron autoxidation and ferric iron reduction. Food Chemistry. Elsevier Ltd., 2008, vol. 106, No 2, p. 650-660. ISSN 0308-8146.
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Basic information
Original name Influence of dietary phenolic acids on redox status of iron: Ferrous iron autoxidation and ferric iron reduction
Name in Czech Vliv fenolových kyselin na redoxní stav železa: oxidace železnatých iontů a redukce železitých iontů
Authors CHVÁTALOVÁ, Kateřina (203 Czech Republic), Iva SLANINOVÁ (203 Czech Republic), Lenka BŘEZINOVÁ (203 Czech Republic) and Jiří SLANINA (203 Czech Republic, guarantor).
Edition Food Chemistry, Elsevier Ltd. 2008, 0308-8146.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 21101 Food and beverages
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.696
RIV identification code RIV/00216224:14110/08:00024823
Organization unit Faculty of Medicine
UT WoS 000250038400029
Keywords in English Iron; Phenolic acids; Polyphenols; Ferrous ion; Ferric ion; Autoxidation; Ferric iron reduction; Metal chelation; Ferroxidase-like activity
Tags Autoxidation, Ferric ion, Ferric iron reduction, Ferrous ion, Ferroxidase-like activity, Iron, Metal chelation, phenolic acids, Polyphenols
Tags International impact, Reviewed
Changed by Changed by: Mgr. Jiří Slanina, Ph.D., učo 689. Changed: 18/6/2009 17:57.
Abstract
All phenolic acids bearing 3,4-dihydroxy (catechol) or 3,4,5-trihydroxy (galloyl) moiety formed chelates with ferric iron and significantly increased the rate of Fe2+ autoxidation. The carboxylate group and catechol substitution instead of galloyl moiety facilitated the ferrous ion oxidation more effectively. Caffeic acid and protocatechuic acid, the strongest accelerators of Fe2+ autoxidation, were able to facilitate autoxidation at concentrations lower than 1% of the initial amount of Fe2+. Therefore chelates of these catecholic acids with iron displayed ferroxidase-like activity. Conversely, when we started from ferric ions, catechols partially formed ferrous ions in the presence of ferrozine. Thus, catecholic acids formed stable chelates with iron, in which ferric ion is the dominant species, but the redox cycling of iron between Fe2+ and Fe3+ in chelates probably plays a crucial role in the catalysis of ferrous iron autoxidation. Interestingly, 3-hydroxybenzoic acid, 4-hydroxybenzoic acid and vanillic (4-hydroxy-3-methoxybenzoic) acid protected ferrous ions from autoxidation as effectively as ascorbic acid and cysteine.
Abstract (in Czech)
Všechny fenolové kyseliny nesoucí 3,4-dihydroxy (katechol) or 3,4,5-trihydroxy (galloyl) skupiny tvořily chelaty s železitými ionty a významně zvyšovaly rychlost autooxidace iontů Fe2+.
Links
GA303/00/D062, research and development projectName: Biologická dostupnost a mechanismus antioxidačního účinku fenolických kyselin a lignanů
Investor: Czech Science Foundation, Bioavailability and mechanism of antioxidant activity of phenolic acids and lignans
GD301/03/H005, research and development projectName: Molekulární a buněčná biologie v biomedicíně
Investor: Czech Science Foundation, Molecular and cell biology in biomedicine
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