包封生物活性大豆蛋白水解物脂质体的制备与表征

Neda Pavlović, J. Jovanovic, Verica B Djordjević, Bojana D. Balanč, B. Bugarski, Z. Knežević-Jugović
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引用次数: 2

摘要

大豆蛋白以其高营养价值和显著的技术功能特性而闻名,可以通过蛋白水解酶水解,从而转化为富含二肽、三肽和寡肽的水解产物。由此产生的肽是有价值的生物活性的载体,这使得大豆水解物作为技术功能和生物活性成分在功能食品中具有重要的应用价值。然而,大豆蛋白水解物的生物利用度低、不稳定、苦味、吸湿性和与食物基质相互作用的可能性阻碍了它们的商业结合和应用。本研究的目的是将大豆蛋白水解物包封在脂质体中,以克服上述缺点,同时保留蛋白水解物所表现出的生物活性。大豆水解物是用商业食品级蛋白酶、解淀粉芽孢杆菌的内蛋白酶(中和酶?)和米曲霉的鸡蛋和内蛋白酶(风味酶?)对大豆浓缩蛋白进行两步酶解制备的,并包被在脂质体中。脂质体是用商用脂质混合物(Phospolipon?90G),主要含有磷脂酰胆碱。然后,用(1)频率为20 kHz的超声波探头和(2)频率为40 kHz的超声波浴产生的高强度超声波处理含有大豆蛋白水解物的多层囊泡(MLV)。探针超声获得了最小(310 nm)和均匀(单峰大小分布)的脂质体,肽包封效率最高(19%)。结果表明,大豆蛋白水解物的掺入是在脂质体膜内实现的,并导致脂质体尺寸在所有测试配方中增加,即:使用超声波探针从297 nm增加到310 nm,使用超声波浴从722 nm增加到850 nm,而在没有超声波处理的配方中,从2818 nm增加到3464 nm。多肽包埋导致脂质体体积增大,zeta电位值负电荷增加,其中MLV脂质体的zeta电位值在-30 mV以下,具有较高的稳定性。通过对ABTS的清除能力和铁螯合活性,证实了探针超声脂质体制剂具有显著的抗氧化活性。在模拟胃肠道条件下进行的释放研究证实,与游离水解物的扩散相比,脂质体可以延长胶囊化大豆蛋白水解物的释放时间。在前75分钟,脂质体包封的大豆肽只有20%扩散,比未包封的大豆水解产物的扩散低2.2倍。脂质体包膜大豆蛋白水解物在食品科学和技术等领域具有广阔的应用前景,可提高食品的营养价值和保质期,开发功能性食品。
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Production and characterization of liposomes with encapsulated bioactive soy protein hydrolysate
Soy proteins known for their high nutritional value and pronounced techno-functional properties, can be hydrolyzed by using proteolytic enzymes and thus converted into hydrolysates rich in di-, tri- and oligopeptides. The resulting peptides are carriers of valuable biological activities, which make the soy hydrolysates very important in functional food applications as techno-functional and bioactive ingredients. However, commercial incorporation and application of soy protein hydrolysates can be hinderedby their low bioavailability and instability, bitter taste, hygroscopicity and possibility to interact with the food matrix. The aim of this research is encapsulation of the soy protein hydrolysate in liposomes in order to overcome the stated shortcomings, while preserving the biological activities that protein hydrolysates exhibit. The soy hydrolysate was prepared by a two-step enzymatic hydrolysis of a soy protein concentrate using commercial food-grade proteases, endoprotease from Bacillus amyloliquefaciens (Neutrase?) and egzo- and endoprotease from Aspergillus oryzae (Flavourzyme?) and encapsulated within liposomes. The liposomes were produced by a thin film method using a commercial lipid mixture (Phospolipon? 90G) containing mainly phosphatidylcholine. Next, the obtained multilamellar vesicles (MLV) with the soy protein hydrolysate were treated by high-intensity ultrasound waves generated by using (1) an ultrasonic probe at a frequency of 20 kHz and (2) an ultrasonic bath with a frequency 40 kHz. The smallest (310 nm) and uniform (unimodal size distribution) liposomes with the highest efficiency of peptide encapsulation (19 %) were obtained by the probe sonication. The presented results showed that incorporation of the soy protein hydrolysates was achieved within the liposome membrane and caused an increase in the liposome size in all tested formulations, namely: from 297 to 310 nm by using the ultrasonic probe, from 722 to 850 nm by using the ultrasonic bath, while in formulations without the ultrasonic treatments the increase from 2818 to 3464 nm was recorded. The entrapped peptides caused enlargement of all liposomes and the increase in negative charge of zeta potential values, which in the case of MLV liposomes was below -30 mV, indicating high stability of these liposomes. Significant antioxidant activity of the probe-sonicated liposomal formulation was confirmed by the ABTS scavenging ability and iron-chelating activity. Release studies conducted under simulated gastrointestinal conditions confirmed that liposomes provide prolonged release of encapsulated soy protein hydrolysates as compared to diffusion of the free hydrolysate. In the first 75 min, only 20 % of liposome encapsulated soy peptides diffused, which is 2.2-fold lower as compared to the diffusion of the non-encapsulated soy hydrolysate. Liposome encapsulated soy protein hydrolysates may provide the possibility for application in the areas such as food science and technology, with the aim to enhance the nutritional value and shelf life of food products, and develop functional foods.
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