β-Carotene autoxidation: oxygen copolymerization, non-vitamin A products, and immunological activity

Author:

Burton Graham W.1,Daroszewski Janusz1,Nickerson James G.2,Johnston James B.3,Mogg Trevor J.1,Nikiforov Grigory B.1

Affiliation:

1. Avivagen Inc., 100 Sussex Drive, Ottawa, ON K1A 0R6, Canada.

2. Avivagen Inc., 550 University Ave., Charlottetown, PE C1A 4P3, Canada.

3. National Research Council of Canada, 550 University Ave., Charlottetown, PE C1A 4P3, Canada.

Abstract

Carotenoids are reported to have immunological effects independent of vitamin A activity. Although antioxidant activity has been suggested as a basis of action, the ability of carotenoids to autoxidize to numerous non-vitamin A products with immunological activity is an alternative yet to be fully explored. We have undertaken a systematic study of β-carotene autoxidation and tested the product mixture for immunological activity. Autoxidation proceeds predominantly by oxygen copolymerization, leading to a defined, reproducible product corresponding to net uptake of almost 8 molar equivalents of oxygen. The product, termed OxC-beta, empirical formula C40H60O15 versus C40H56 for β-carotene, contains more than 30% oxygen (w/w) and 85% β-carotene oxygen copolymers (w/w) as well as minor amounts of many C8−C18 norisoprenoid compounds. No vitamin A or higher molecular weight norisoprenoids are present. The predominance of polymeric products has not been reported previously. The polymer appears to be a less polymerized form of sporopollenin, a biopolymer found in exines of spores and pollen. Autoxidations of lycopene and canthaxanthin show a similar predominance of polymeric products. OxC-beta exhibits immunological activity in a PCR gene expression array, indicating that carotenoid oxidation produces non-vitamin A products with immunomodulatory potential.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

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