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A novel directed enzymolysis strategy for the preparation of umami peptides in Stropharia rugosoannulata and its mechanism of taste perception

文献类型: 外文期刊

作者: Chen, Daoyou 1 ; Rong, Mingli 1 ; Tang, Shuting 4 ; Zhang, Chuanxi 3 ; Wei, Hao 3 ; Yuan, Zhaoting 1 ; Miao, Tingwei 1 ; Song, Hucheng 1 ; Jiang, Haiming 5 ; Yang, Yan 2 ; Zhang, Lujia 1 ;

作者机构: 1.East China Normal Univ, Shanghai Engn Res Ctr Mol Therapeut & New Drug Dev, Sch Chem & Mol Engn, Shanghai 200062, Peoples R China

2.Shanghai Acad Agr Sci, Inst Edible Fungi, Natl Engn Res Ctr Edible Fungi, Key Lab Edible Fungi Resources & Utilizat South,Mi, 1000 Jinqi Rd, Shanghai 201403, Peoples R China

3.Shanghai Jiao Tong Univ, Sch Elect Informat & Elect Engn, Dept Micro Nano Elect, Shanghai 200240, Peoples R China

4.Shihezi Univ, Sch Food Sci & Technol, Shihezi 832000, Peoples R China

5.Inner Mongolia Univ Sci & Technol, Sch Life Sci & Technol, Baotou 014010, Peoples R China

关键词: Stropharia rugosoannulata; Directed enzymolysis; Virtual screening; Umami peptide; Molecular simulation

期刊名称:FOOD CHEMISTRY ( 影响因子:9.8; 五年影响因子:9.7 )

ISSN: 0308-8146

年卷期: 2025 年 468 卷

页码:

收录情况: SCI

摘要: This study aimed to explore the effect of directed enzymolysis on the umami characteristics of S. rugosoannulata, clarify the flavour formation mechanism of umami peptides. We expressed a new aminopeptidase (DNPEP) and obtained the umami peptides of S. rugosoannulata by alkaline protease and DNPEP. The optimal enzymolysis conditions were temperature 55 degrees C, solid-liquid ratio 1:20 (g/mL), alkaline protease enzymolysis (60 min, 0.5 %, pH 9.0), and DNPEP enzymolysis (80 min, 0.3 %, pH 8.0). The umami peptide components were separated by ultrafiltration and gel filtration chromatography. Six umami peptides (EEAKFN, KAELDLH, LADVEEDK, LKEAHDVA, AHLDYGDGK, and LGKSEDDVSK) were identified by LC-MS/MS and virtual screening, and the umami thresholds of the peptides were 0.15-1.09 mmol/L. Molecular simulations revealed that the amino acid residues Glu301, Ser217, Asp218, and Arg277 were crucial in the binding of the umami peptide to the T1R1/ T1R3. Therefore, this study provides a theoretical basis for the development of mushroom condiments.

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