Sachiko Takagi

Bio: Sachiko Takagi is an academic researcher from Kobe Gakuin University. The author has contributed to research in topics: Roasting & Fatty acid. The author has an hindex of 12, co-authored 16 publications receiving 548 citations.

Effects of seed roasting temperature and time on the quality characteristics of sesame (Sesamum indicum) oil

Abstract: The quality characteristics and composition of sesame oils prepared at different roasting temperatures (160–250°C) from sesame seeds using a domestic electric oven were evaluated as compared to an unroasted oil sample: only minor increases (P<0·05) in characteristics, such as peroxide value, carbonyl value, anisidine value and thiobarbituric acid reactive substances, of sesame oils occurred in relation to increasing roasting temperature and time between 160 and 200°C, but colour units of oils increased markedly over a 220°C roasting temperature. Significant decreases (P<0·05) were observed in the amounts of triacylglycerols and phospholipids in the oils prepared using a 250°C roasting temperature. The amounts of γ-tocopherol and sesamin still remained over 80 and 90%, respectively, of the original levels after roasting at 250°C. In the oil prepared using a 250°C roasting temperature, sesamol was detected at 3370 mg per kg oil, but sesamolin was almost depleted after 25 min of roasting. Burning and bitter tastes were found in the oils prepared at roasting temperatures over 220°C. The results suggested that a high-quality product would be obtained by roasting for 25 min at 160 or 180°C, 15 min at 200°C and 5 min at 220°C when compared with the other samples. © 1997 SCI.

Variations in the composition of various acyl lipids, tocopherols and lignans in sesame seed oils roasted in a microwave oven

Abstract: Seeds from various strains of cultivated Sesamum indicum Linn (colour of seeds : black, brown and white) were exposed to microwave roasting for 16 and 30 min at a frequency of 2450 MHz and were studied not only for different acyl lipids and their fatty acid compositions, but also for the contribution of antioxidants to the oxidative stability of the oils. Lipids from all-seeded strains were comparable in their total fatty acid composition, with linoleic, oleic, stearic and palmitic acids as the major acids. The total lipids were isolated by thin-layer chromatography into the following five fractions : triacylglycerols (TAG), di-acylglycerols, free fatty acids, polar lipids and steryl esters. The TAG were slightly and randomly hydrolysed by microwaves, but was still representing 900 g kg -1 of the total lipids at 30 min of roasting. Although burning and bitter tastes occurred at the time, the tocopherols and lignans still amounted to over 80% of the original level. The results suggested that the oxidative stability of the oils would probably be due to the synergism between endogenous antioxidants and browning substances produced during microwave roasting.

Antioxidative effects of sesamol and tocopherols at various concentrations in oils during microwave heating

Abstract: The effectiveness of sesamol and tocopherols or their mixtures at different concentrations (50 to 800 ppm) on the oxidative stability of tocopherol-stripped oils was studied under microwave heating conditions. Microwave heating accelerated the oxidation of the purified substrate oils. The oxidative deterioration of the oils was significantly (P<0.05) retarded during microwave heating by the addition of sesamol or tocopherols, and also mixtures of these antioxidants. A combination of sesamol and γ-tocopherol was more efficient than that of sesamol and the other tocopherol homologues in inhibiting hydroperoxide formation in the oils. Useful levels of these antioxidants were 400 ppm for tocopherols and 50–400 ppm for sesamol. In general, the residual amount of sesamol in the oils during microwave heating was significantly greater (P<0.05) than that of tocopherols. Very effective combinations of tocopherols and sesamol as antioxidants for the purified oils were 200 or 400 ppm of γ-tocopherol and 50, 200 or 400 ppm of sesamol, respectively. © 1999 Society of Chemical Industry

Roasting effects on fatty acid distributions of triacylglycerols and phospholipids in sesame (Sesamum indicum) seeds

Abstract: Sesame seeds were roasted at different temperatures (180–220 °C) using a domestic electric oven. The positional distribution of fatty acids in triacylglycerols (TAGs) and phosphatidylcholine (PC) isolated from total lipids in these seeds was investigated as well as the naturally occurring antioxidants that are present. Major lipid components were TAGs and phospholipids (PLs), while steryl esters (SEs), free fatty acids (FFAs) and sn-1,3- and sn-1,2-diacylglycerols (DAGs) were minor ones. Following roasting, a significant increase (P < 0.05) was observed in FFAs and in both forms of DAG (primarily sn-1,3-DAG). The greatest PL losses (P < 0.05) were observed in phosphatidylethanolamine (PE), followed by PC and phosphatidylinositol (PI). On the other hand, the amounts of γ-tocopherol and sesamin remained at over 80 and 90% respectively of the original levels after roasting at 220 °C. The principal characteristics of the positional distribution of fatty acids were still retained after 25 min of roasting: unsaturated fatty acids, especially linoleic and/or oleic, were predominantly concentrated in the sn-2-position, and saturated fatty acids, especially stearic and/or palmitic, primarily occupied the sn-1- or sn-3-position. The results suggest that unsaturated fatty acids located in the sn-2-position are significantly protected from oxidation during roasting at elevated temperatures. © 2001 Society of Chemical Industry

Mechanisms and Factors for Edible Oil Oxidation

Abstract: : Edible oil is oxidized during processing and storage via autoxidation and photosensitized oxidation, in which triplet oxygen (3O2) and singlet oxygen (1O2) react with the oil, respectively. Autoxidation of oils requires radical forms of acylglycerols, whereas photosensitized oxidation does not require lipid radicals since 1O2 reacts directly with double bonds. Lipid hydroperoxides formed by 3O2 are conjugated dienes, whereas 1O2 produces both conjugated and nonconjugated dienes. The hydroperoxides are decomposed to produce off-flavor compounds and the oil quality decreases. Autoxidation of oil is accelerated by the presence of free fatty acids, mono- and diacylglycerols, metals such as iron, and thermally oxidized compounds. Chlorophylls and phenolic compounds decrease the autoxidation of oil in the dark, and carotenoids, tocopherols, and phospholipids demonstrate both antioxidant and prooxidant activity depending on the oil system. In photosensitized oxidation chlorophyll acts as a photosensitizer for the formation of 1O2; however, carotenoids and tocopherols decrease the oxidation through 1O2 quenching. Temperature, light, oxygen concentration, oil processing, and fatty acid composition also affect the oxidative stability of edible oil.

Characterization of the total free radical scavenger capacity of vegetable oils and oil fractions using 2,2-diphenyl-1-picrylhydrazyl radical.

Abstract: The total free radical scavenger capacity (RSC) of 57 edible oils from different sources was studied: olive (24 brands of oils), sunflower (6), safflower (2), rapeseed (3), soybean (3), linseed (2), corn (3), hazelnut (2), walnut (2), sesame (2), almond (2), mixture of oils for salad (2), “dietetic” oil (2), and peanut (2). Olive oils were also studied according to their geographical origins (France, Greece, Italy, Morocco, Spain, and Turkey). RSC was determined spectrophotometrically by measuring the disappearance of the radical 2,2-diphenyl-1-picrylhydrazyl radical (DPPH•) at 515 nm. The disappearance of the radical followed a double-exponential equation in the presence of oils and oil fractions, which suggested the presence of two (fast and slow) groups of antioxidants. RSC was studied for the methanol-soluble phase (“methanolic fraction”, MF) of the oil, the fraction nonsoluble in methanol (“lipidic fraction”, LF), and the nonfractionated oil (“total oil”; TF = MF + LF). Only olive, linseed, rapeseed...