Tang Xuhua, Feng Shouyu, Liu Yanwei, Zhu Wenhui, Bu Ying, Li Jianrong, Liu Cikun, Li Xuepeng
College of Food Science and Engineering, Bohai University, Jinzhou 121013, China.
College of Food Science and Engineering, Bohai University, Jinzhou 121013, China.
Int J Biol Macromol. 2025 Apr;304(Pt 1):140876. doi: 10.1016/j.ijbiomac.2025.140876. Epub 2025 Feb 12.
Umami peptides were screened and identified from the enzymatic hydrolysate of Spanish mackerel head and its Maillard reaction products using ultrafiltration, gel chromatography, and LC-MS/MS (Liquid Chromatography-Tandem Mass Spectrometry). The umami properties of these peptides were subsequently evaluated and characterized using electronic tongue analysis and molecular docking. This study is the first to employ enzymatic hydrolysis combined with Maillard reaction for the preparation of umami peptides from Spanish mackerel head. Following this approach, a total of nine novel umami peptides were identified, including five from enzymatic hydrolysate (YDDKIY, ITPDEKGTTF, DAITTDDAGK, LEDGYPKEIQE, DAITPDEKGTTF) and four from Maillard reaction products (KDEGSDV, TPDEKGT, TEKAKGEP, FDAITPDEKGTTF). Sensory evaluation and electronic tongue analysis confirmed their distinct umami properties, with taste recognition thresholds ranging from 0.125 to 0.25 mg/mL. Molecular docking analysis revealed that these peptides interact with the T1R1/T1R3 umami receptor through hydrogen bonding and hydrophobic interactions, with key binding residues identified as Ser150, Ser256, and Glu128. This study provides a novel methodology for screening umami peptides from seafood by-products and lays the groundwork for their application as natural umami enhancers in the food industry.
利用超滤、凝胶色谱和液相色谱-串联质谱法(LC-MS/MS)从鲅鱼头酶解产物及其美拉德反应产物中筛选并鉴定了鲜味肽。随后,采用电子舌分析和分子对接对这些肽的鲜味特性进行了评估和表征。本研究首次采用酶解结合美拉德反应从鲅鱼头制备鲜味肽。按照这种方法,共鉴定出9种新型鲜味肽,其中5种来自酶解产物(YDDKIY、ITPDEKGTTF、DAITTDDAGK、LEDGYPKEIQE、DAITPDEKGTTF),4种来自美拉德反应产物(KDEGSDV、TPDEKGT、TEKAKGEP、FDAITPDEKGTTF)。感官评价和电子舌分析证实了它们独特的鲜味特性,味觉识别阈值为0.125至0.25mg/mL。分子对接分析表明,这些肽通过氢键和疏水相互作用与T1R1/T1R3鲜味受体相互作用,确定关键结合残基为Ser150、Ser256和Glu128。本研究为从海产品副产物中筛选鲜味肽提供了一种新方法,并为其在食品工业中作为天然鲜味增强剂的应用奠定了基础。