王 静,方 丹,刘诗佳,邓雅之,毛招羽,李 佳,王婧扬,冯莉萍.核桃多肽-硒螯合物的制备及其理化性质研究[J].食品安全质量检测学报,2025,16(15):213-221
核桃多肽-硒螯合物的制备及其理化性质研究
Preparation and physicochemical properties research of Juglans regia L. polypeptide-selenium chelate
投稿时间:2025-01-21  修订日期:2025-05-18
DOI:
中文关键词:  核桃多肽-硒螯合物,理化性质,稳定性,体外消化,抗氧化能力
英文关键词:Juglans regia L. polypeptide-selenium chelate  physicochemical properties  stability  in vitro digestion  antioxidant capacity
基金项目:
作者单位
王 静 1.陕西学前师范学院生物食品与化学学院 
方 丹 1.陕西学前师范学院生物食品与化学学院 
刘诗佳 1.陕西学前师范学院生物食品与化学学院 
邓雅之 1.陕西学前师范学院生物食品与化学学院 
毛招羽 1.陕西学前师范学院生物食品与化学学院 
李 佳 1.陕西学前师范学院生物食品与化学学院 
王婧扬 1.陕西学前师范学院生物食品与化学学院 
冯莉萍 1.陕西学前师范学院生物食品与化学学院 
AuthorInstitution
WANG Jing 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
FANG Dan 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
LIU Shi-Jia 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
DENG Ya-Zhi 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
MAO Zhao-Yu 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
LI Jia 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
WANG Jing-Yang 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
FENG Li-Ping 1.College of Biology, Food and Chemistry, Shaanxi Xueqian Normal University 
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中文摘要:
      目的 探究核桃多肽-硒螯合物的制备方法及其理化性质。方法 采用碱溶酸沉法提取核桃蛋白, 经碱性蛋白酶酶解后制得核桃多肽。核桃多肽再与亚硒酸钠反应, 生成核桃多肽-硒螯合物。通过单因素试验和正交试验, 优化制备工艺。结果 在多肽与亚硒酸钠质量比为3:1、螯合温度45 ℃、螯合时间50 min、pH 8的条件下, 硒螯合率达到最高, 为58.99%±1.44%。该螯合物耐热、耐酸碱, 消化稳定性好, 硒生物利用率高。与核桃多肽相比, 核桃多肽-硒螯合物具有更强的1,1-二苯基-2-苦味酰肼(1,1-diphenyl-2-picrylhydrazyl, DPPH)自由基、羟基自由基和2,2’-联氮-二(3-乙基-苯并噻唑-6-磺酸)二铵盐[2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), ABTS]阳离子自由基清除能力。结论 本研究制备了核桃多肽-硒螯合物, 优化了制备工艺, 并发现其具有良好的理化性质和抗氧化能力, 为开发补硒产品提供了原料参考。
英文摘要:
      Objective To study the preparation and physicochemical properties of polypeptide-selenium chelate from Juglans regia L.. Methods Juglans regia L. protein was extracted by alkali-soluble acid precipitation method, and Juglans regia L. polypeptide was prepared by alkaline protease. Juglans regia L. polypeptide reacted with sodium selenite to produce Juglans regia L. polypeptide-selenium chelate. The preparation technology was optimized by single factor test and orthogonal test. Results When the mass ratio of polypeptide to sodium selenite was 3:1, the chelating temperature was 45 ℃, the chelating time was 50 min, and the pH was 8, the chelating rate was 58.99%±1.44%. The chelate was resistant to heat, acid and alkali, had good digestive stability and high bioavailability of selenium. Compared with Juglans regia L. polypeptide, Juglans regia L. polypeptide-selenium chelate had stronger scavenging ability of 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical, hydroxyl free radical and 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) cation free radical. Conclusion In this study, Juglans regia L. polypeptide-selenium chelate is successfully prepared through optimized synthesis conditions. The resulting complex demonstrates favorable physicochemical properties and significant antioxidant capacity, providing a potential raw material reference for developing selenium-enriched nutritional supplements.
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