4.7 Article

Flavonoids enhance gel strength of ovalbumin: Properties, structures, and interactions

Journal

FOOD CHEMISTRY
Volume 387, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2022.132892

Keywords

Egg white protein; Flavonoids; Hydrogel; Interaction; Gel strength

Funding

  1. Jiangxi Provincial Natural Science Foundation [20212BAB205037]
  2. High-level Talents' Scientific Research Foundation of Gannan Medical University [QD202123]
  3. National Natural Science Foundation of China [31660471, 32060558]

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This study investigated the effect of ovalbumin-flavonoid interactions on the formation and properties of ovalbumin hydrogels. The results showed that flavonoids were able to promote the gelation of low concentration ovalbumin solution, resulting in more elastic hydrogels. Among the flavonoids tested, naringenin and ovalbumin formed hydrogels with the strongest gel hardness, springiness, and water holding capacity. Fluorescence spectroscopy and molecular docking analysis revealed that the main interactions between ovalbumin and flavonoids were hydrogen bonds or hydrophobic forces, depending on the specific flavonoid. Flavonoids with more phenolic hydroxyl groups and a C2 = C3 double bond had higher affinity to ovalbumin. This research provides new insights into the mechanism of ovalbumin-flavonoid interactions and their influence on hydrogel formation and properties.
The effect of ovalbumin-flavonoids (naringenin, genistein, naringin, puerarin, and daidzein) interactions on the formation and properties of ovalbumin hydrogels was investigated. The results suggested that flavonoids were able to promote the gelation of low concentration ovalbumin solution, which was not able to form hydrogel upon heating. All hydrogels formed by flavonoids and ovalbumin were more elastic than viscous. The hydrogels formed by naringenin and ovalbumin showed the strongest gel hardness, springiness, and water holding capacity. Fluorescence spectroscopy and molecular docking analysis revealed that the main interactions between ovalbumin and naringenin, genistein, puerarin, naringin were hydrogen bond, while the main interaction between ovalbumin and daidzein was hydrophobic force. Flavonoids, which have a structure with more phenolic hydroxyl groups, a C2 = C3 double bond and dehydrogenated glycosides, possessed higher affinity to ovalbumin. This research provides new insights into mechanism of ovalbumin-flavonoids interactions and its influence on the formation and property of hydrogel.

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