Anuduang Artorn, Ounjaijean Sakaewan, Phongphisutthinant Rewat, Pitchakarn Pornsiri, Chaipoot Supakit, Taya Sirinya, Parklak Wason, Wiriyacharee Pairote, Boonyapranai Kongsak
Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.
The Traditional Food Research and Development Unit, Multidisciplinary Research Institute (MDRI), Chiang Mai University, Chiang Mai 50200, Thailand.
Foods. 2024 Sep 25;13(19):3041. doi: 10.3390/foods13193041.
The non-enzymatic conjugation of peptides through the Maillard reaction has gained attention as an effective method to enhance biological functions. This study focuses on two conjugate mixtures: crude soy protein hydrolysate (SPH) conjugated with mannose (SPHM) and crude soy protein hydrolysate conjugated with allulose (SPHA). These two mixtures were products of the Maillard reaction, also known as non-enzymatic glycation. In vitro experiments were conducted to evaluate the antioxidant, anti-pancreatic lipase, inhibition of Bovine Serum Albumin (BSA) denaturation, and anti-angiotensin converting enzyme (ACE) activities of these conjugated mixtures. The results indicate that conjugated mixtures significantly enhance the antioxidant potential demonstrated via the DPPH and FRAP assays. SPHA exhibits superior DPPH scavenging activity (280.87 ± 16.39 µg Trolox/mL) and FRAP value (38.91 ± 0.02 mg Trolox/mL). Additionally, both conjugate mixtures, at a concentration of 10 mg/mL, enhance the BSA denaturation properties, with SPHM showing slightly higher effectiveness compared to SPHA (19.78 ± 2.26% and 5.95 ± 3.89%, respectively). SPHA also shows an improvement in pancreatic lipase inhibition (29.43 ± 1.94%) when compared to the SPHM (23.34 ± 3.75%). Furthermore, both the conjugated mixtures and rare sugars exhibit ACE inhibitory properties on their own, effectively reducing ACE activity. Notably, the ACE inhibitory effects of the individual compounds and their conjugate mixtures (SPHM and SPHA) are comparable to those of positive control (Enalapril). In conclusion, SPHM and SPHA demonstrate a variety of bioactive properties, suggesting their potential use in functional foods or as ingredients in supplementary products.
通过美拉德反应进行肽的非酶共轭作为增强生物学功能的有效方法已受到关注。本研究聚焦于两种共轭混合物:与甘露糖共轭的粗大豆蛋白水解物(SPH-M)和与阿洛酮糖共轭的粗大豆蛋白水解物(SPH-A)。这两种混合物是美拉德反应的产物,也称为非酶糖基化。进行了体外实验以评估这些共轭混合物的抗氧化、抗胰脂肪酶、抑制牛血清白蛋白(BSA)变性和抗血管紧张素转换酶(ACE)活性。结果表明,共轭混合物通过DPPH和FRAP测定法显著增强了抗氧化潜力。SPH-A表现出优异的DPPH清除活性(280.87±16.39μg Trolox/mL)和FRAP值(38.91±0.02mg Trolox/mL)。此外,两种共轭混合物在浓度为10mg/mL时均增强了BSA变性特性,与SPH-A相比,SPH-M显示出略高的有效性(分别为19.78±2.26%和5.95±3.89%)。与SPH-M(23.34±3.75%)相比,SPH-A在抑制胰脂肪酶方面也有所改善(29.43±1.94%)。此外,共轭混合物和稀有糖自身均表现出ACE抑制特性,有效降低了ACE活性。值得注意的是,各化合物及其共轭混合物(SPH-M和SPH-A)的ACE抑制作用与阳性对照(依那普利)相当。总之,SPH-M和SPH-A表现出多种生物活性特性,表明它们在功能性食品或作为补充产品成分方面具有潜在用途。