Formation of apocarotenals and epoxycarotenoids from β-carotene by chemical reactions and by autoxidation in model systems and processed foods

Author(s)

Rodriguez‚ E.B. ; Rodriguez-Amaya‚ D.B.

• Document type: Journal article
• Source: Food Chemistry; v. 101, n. 2, p. 563-572, 2007.

Abstract

It is generally accepted that oxidation of carotenoids begins with epoxidation and cleavage to apocarotenals. However, systematic studies to demonstrate occurrence of these reactions are lacking. In this study, the products formed by epoxidation with m-chloroperbenzoic acid (MCPBA), oxidative cleavage with KMnO4 and autoxidation in model systems, in the presence and absence of light, at ambient condition were identified. The presence of oxidation products was also verified in processed products. beta-carotene-5,6-epoxide, beta-carotene-5,8-epoxide, beta-carotene-5,6,5',6'-diepoxide, beta-carotene-5,6,5',8'-diepoxide and P-carotene 5,8,5',8'-diepoxide were formed by the reaction of beta-carotene with MCPBA. The oxidation products with KMnO4 were identified as beta-apo-8'-carotenal, beta-apo-10'-carotenal, beta-apo-12'-carotenal, beta-apo-14'-carotenal and beta-apo-15-carotenal, along with semi-beta-caroten one and monohydroxy-beta-carotene5,8-epoxide. Except for beta-carotene 5,6,5',6'-diepoxide, these products were detected in the model systems. Some of these products were also found in mango juice, acerola juice and dried apricot. Increased Z-isomerization was also observed and Z-isomers of the oxidation products were detected. (c) 2006 Elsevier Ltd. All rights reserved. (AU)

• FAPESP's process: 03/10151-4 - Bioactive substances in food: chemical, biochemical, technological aspects and implications in human health
• Grantee: Delia Rodriguez Amaya
• Support Opportunities: PRONEX Research - Thematic Grants