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Natural Antioxidants: Occurrence and Their Role in Food Preservation  49
  VetBooks.ir  is site for tocol biosynthesis and the aromatic amino acid tyrosine is consid-


            ered to be its precursor. The mechanism of biosynthesis of tocols involves
            coupling of phytyl diphosphate with homogenestic acid (2,5-dihydroxyphen-
            ylacetic acid), followed by cyclization and methylation reactions. Vitamin E
            compounds include the tocopherols and tocotrienols. Tocotrienols have a
            conjugated triene double bond system in the phytyl side chain, while tocoph-
            erols do not.  Methyl  substitution  affects  the  bioactivity  of vitamin  E, as
            well as its in vitro antioxidant activity. Tocopherols or vitamin E have eight
            known homologues, that is, α-, β-, γ-, δ- tocopherols and α-, β-, γ-, δ- toco-
            trienols. Tocopherols are fat-soluble antioxidants that function as scaven-
            gers of lipid peroxyl radicals. Tocopherols’ content is found to be related to
            RSA and antioxidant activity of oils. Tocopherols’ content decreases during
            processing of oils. There have been many reports on the protective effect of
            tocopherols as food antioxidants (Dougherty, 1988). Tocopherols protect PL
            and cholesterol against oxidation (Faustman et al., 1989; Li et al., 1996).
            Total tocopherol content and major tocopherol homologues differ from one
            oil to another (Table 2.1 and Fig. 2.1). The level of tocopherols decreases
            with time of storage and heating of oils (Li et al., 1996).












                         R'
                                      ·  a/p/7a-tocopherol   -CH3   -CH3

                                      beta-tocopherol    -CH3        -H
                                      gamma-tocopherol     -H     -CH3
                                      delta-tocopherol     -H        -H

                         CH3
                  R"




                         R'             tocomeools

            FIGURE 2.1  Different tocopherol homologues of vegetable oils.
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