Arslan Derya, Demir M Kürşat, Acar Ayşenur, Arslan Fatma Nur
Department of Food Engineering, Faculty of Engineering and Architecture, Necmettin Erbakan University, Koycegiz Campus, Konya, Turkey.
Department of Chemistry, Faculty of Science, Karamanoğlu Mehmetbey University, Karaman, Turkey.
Food Technol Biotechnol. 2020 Sep;58(3):348-355. doi: 10.17113/ftb.58.03.20.6638.
Utilization 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.
In 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.
Steaming 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, -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.
This 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.
由于小麦胚芽和小麦胚芽油具有较高的酶活性且含有不饱和脂肪酸,其利用受到限制,这需要采用稳定化技术来解决该问题。
在本研究中,评估了稳定化方法(90℃和160℃的干对流烘箱加热、180W和360W的微波辐射以及高压釜蒸煮)对小麦胚芽及其油脂的影响。
蒸煮导致脂氧合酶活性、游离脂肪酸含量、DPPH自由基清除活性以及生育酚和生育三烯酚的质量分数发生最显著变化。在经对流加热(160℃)和100℃以上蒸煮处理的油样中测得较低的过氧化值。然而,高温处理样品的对茴香胺值明显高于低温稳定化处理的样品。160℃的烘箱加热也是蒸煮后最有效的脂氧合酶失活处理方法之一。蒸煮显著降低了总生育酚的质量分数,这与β - 生育酚含量的更大损失直接相关。相反,γ - 和δ - 生育酚以及生育三烯酚同系物在蒸煮样品中的含量更高。α - 生育酚和γ - 生育三烯酚是对稳定化过程最具抗性的异构体。
本研究表明,工业上广泛用于小麦胚芽热稳定化的高温烘箱加热方法,与蒸煮和微波处理相比,在氧化稳定性方面并无优势。蒸煮延缓了胚芽中的氧化,同时进一步抑制了脂氧合酶活性。此外,生育三烯酚更易于保存。在工业应用中,低功率微波(180W而非360W)和较低温度(90℃而非160℃)的烘箱加热更为可取。