Abstract

SUMMARYResearch backgroundUtilization of wheat germ and wheat germ oil is limited due to high enzymatic activity and the presence of unsaturated fatty acids, which require stabilization techniques to overcome this problem.Experimental approachIn this study, the effects of stabilization methods (dry convective oven heating at 90 and 160 °C, microwave radiation at 180 and 360 W, and autoclave steaming) on both wheat germ and its oil were evaluated.Results and conclusionsSteaming caused the most dramatic changes in lipoxygenase activity, free fatty acid content, DPPH radical scavenging activity, and mass fractions of tocopherols and tocotrienols. Lower peroxide values were measured in the oil samples treated with convectional heating (160 °C) and steaming at temperatures above 100 °C. However, p-anisidine values of samples treated at higher temperatures were considerably greater than those of samples stabilized at lower temperatures. Oven heating at 160 °C was also one of the most effective treatments, after steaming, for the inactivation of lipoxygenase. Steaming significantly reduced mass fraction of total tocopherols, which was directly associated with the greater loss of β-tocopherol content. On the contrary, γ- and δ-tocopherol and tocotrienol homologues were abundant with higher amounts in steamed samples. α-Tocopherol and γ-tocotrienol were the most resistant isomers to stabilization processes.Novelty and scientific contributionThis study shows that the high temperature oven heating method, which is widely used in the industry for thermal stabilization of wheat germ, does not provide an advantage in oxidative stability compared to steaming and microwave applications. Steaming delayed oxidation in the germ, while further inhibiting lipoxygenase activity. Moreover, tocotrienols were more conservable. In industrial application, low-power microwave (180 instead of 360 W) and oven heating at lower temperature (90 instead of 160 °C) would be preferable.

Highlights

  • Wheat germ is a highly nutritional product, which contains about 10–15 % lipids, 26– 35 % proteins, 17 % sugars, 1.5–4.5 % fibre and 4 % minerals [1]

  • P-anisidine values of samples treated at higher temperatures were considerably greater than those of samples stabilized at lower temperatures

  • It is well known that the oxidative stability of wheat germ is commonly improved by means of heat treatments which reduce the peroxide number and increase the antioxidant activity

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Summary

Introduction

Wheat germ is a highly nutritional product, which contains about 10–15 % lipids, 26– 35 % proteins, 17 % sugars, 1.5–4.5 % fibre and 4 % minerals [1]. The ratio of polyunsaturated fatty acids, mainly linoleic and linolenic acids, is quite high (almost 80 % of the oil) [3]. Its oil has an important place in the food, medicine and cosmetics industry [6]. The mechanical processes applied during wheat milling cause the cells to break down and the intracellular oil becomes more prone to oxidation. Degradation occurs by the action of oxidative and hydrolytic enzymes such as lipase and lipoxygenase (LOX) on unsaturated fatty acids [1]. Lipase and LOX inactivation are required to prolong the storage stability of the wheat germ.

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