Preparation, structural characterization, and calcium-binding gastrointestinal digestion stability study of phosvitin phosphopeptide-dextran conjugates

  • HAO Chunyan ,
  • ZHI Hongli ,
  • ZHAO Wei ,
  • ZHANG Yaxin ,
  • LIU Huiping ,
  • ZHANG Xiaowei
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  • (College of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin 300457, China)

Received date: 2024-12-11

  Revised date: 2025-02-28

  Online published: 2025-11-03

Abstract

Calcium deficiency has a significant impact on human health, and some calcium supplements (such as peptide-calcium complexes) will reduce the bioavailability due to the gastrointestinal environment.Therefore, the development of new calcium delivery systems with higher calcium binding capacity and better stability is an important strategy to solve this problem.In this study, the conjugates of phosvitin phosphopeptide and dextran (PPP-DX) were prepared by wet Maillard reaction, and the preparation conditions of PPP-DX were optimized by the index of grafting degree.The structure of PPP-DX was characterized by Fourier transform infrared spectroscopy, circular dichroism, fluorescence spectroscopy, and scanning electron microscopy.The calcium-binding capacity and in vitro digestion stability of PPP-DX were also investigated.The results showed that the optimum preparation conditions of PPP-DX were as follows:the mass ratio of PPP to DX was 1∶3, pH was 7, reaction time was 185 min, and reaction temperature was 90 ℃.The grafting degree of PPP-DX was (39.12±0.43)%.Fourier transform infrared spectroscopy showed that the amino group of PPP reacted with the carbonyl group of dextran, and the Maillard reaction could cause CO stretching vibration, as well as C—H and N—H deformation vibration.Compared with PPP, the content of α-helix and β-turn decreased by 52.04% and 47.10%, respectively, and the content of β-sheet increased by 62.93%, which changed the secondary structure of PPP-DX.At the same time, the fluorescence intensity of PPP-DX decreased, and the surface structure of PPP-DX was observed by scanning electron microscopy to be flake and uneven.Compared with PPP-Ca, the calcium-binding capacity of PPP-DX-Ca increased from (74.33±4.39) mg/g to (159.06±2.19) mg/g, increased by 1.14 times, and the calcium release rate in gastric juice decreased from (72.33±2.08)% of PPP-Ca to (43.33±1.52)% of PPP-DX-Ca.PPP-DX resisted the digestion of gastric juice to a certain extent, slowed down the release of calcium ions, made more calcium ions enter the intestinal juice, and improved the stability of calcium in gastric juice.This study indicated that PPP-DX could be used as an effective delivery carrier for new calcium supplements, providing a scientific basis for the development of new high-efficiency calcium supplements.

Cite this article

HAO Chunyan , ZHI Hongli , ZHAO Wei , ZHANG Yaxin , LIU Huiping , ZHANG Xiaowei . Preparation, structural characterization, and calcium-binding gastrointestinal digestion stability study of phosvitin phosphopeptide-dextran conjugates[J]. Food and Fermentation Industries, 2025 , 51(19) : 183 -191 . DOI: 10.13995/j.cnki.11-1802/ts.041825

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