Contribution of low molecular weight antioxidants to the antioxidant screen of germinated soybean seeds

Abstract

Soybean seed of the Mazovia variety (Glycine max) were germinated in the dark at a constant temperature of 25°C up to 168 h (24 h × 7). Changes in content of low molecular weight antioxidants (LMWA) in the course of germination were studied. The analyzed compounds were: total phenolics, soluble proteins, tocopherols (α-T, β-T, γ -T, δ -T), reduced and oxidized glutathione, L-ascorbic acid and L-dehydroascorbic acid. The changes in total antioxidant status (TAS) and the peroxyl radical-trapping capacity (PRTC) of the processed seeds were measured and compared to those of the raw seeds. On the basis of data obtained, the contribution of LMWA to the TAS of raw and germinated soybean seeds was calculated. The results showed a very high molar percentage contribution of phenolic compounds (49.7%) in opposition to glutathione (7.0%), tocopherols (4.0%) and soluble protein (5.7%) to the total TAS of raw soybean seeds. The germination process led to the increased contribution of phenolic compounds (67.7%), soluble proteins (9.3%) and ascorbic acid (4.4%) to the total TAS of germinated seeds and as a result, a decrease in the antioxidant gap was observed compared to the total TAS of raw soybean seeds. This study showed that the contribution of experimentally obtained total PRTC to the total TAS of raw and germinated soybean seeds after seven days ofthe process was 48% and 25.2%, respectively. The PRTC results were comparable to those obtained in TAS only when calculation was done by multiple mean values for content of investigated compounds and their relative potency with respect to Trolox. The PRTC values obtained in this manner were higher than those obtained experimentally indicating that high molecular weight antioxidants as well as are able to quench peroxyl radicals as well as low molecular weight antioxidants. Therefore, calculation of PRTC is a more accurate method that eliminates the puzzling question of unidentified antioxidants shown as the antioxidant gap in the TAS assay.