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Polyphenols complexes were extracted from Common millet (CM), Long-grain rice (LGR) and Huaihe wheat (HW), purification method, components and functional characteristics were studied. Higher phenol content (18.7 in CM, 12.9 in LGR and 22.3 mg g −1 in HW) was obtained by the high-speed shear, with high antioxidants (DPPH 89.2% in HW, ABTS 81.6% in LGR, FRAP 0.83 in HW) after purified. Thirteen typical polyphenol complexes were identified from 21 peaks by UHPLC-LTQ-Orbitrap-MS/MS. Gingerenone A was first detected in CM, HW and LGR; (+/−)-Gingerol was first detected in CM and HW. Morphology by TEM displayed a rough spherical structure with 200-500 nm. Peculiarly contained hydroxyl polyphenol (5-(3,4-Dihydroxyphenyl) valeric acid, Apigenin-8-C-xylosyl-6-C-glucoside), polyphenols with B-rings (Trans-cinnamic acid, Gingerenone A) and the highest contents (+/−)-Gingerol with hydroxyl and Sinapinic acid with B-rings, CM had a higher α-amylase inhibition rate (80.5%) than LGR and HW, which providing a foundation for the development of hypoglycaemic drugs.

BACKGROUND Whey protein‐epigallocatechin gallate (WP‐EGCG) covalent conjugates and non‐covalent nanocomplexes were prepared and compared using Fourier‐transform infrared spectra. The effect of pH (at 2.6, 6.2, 7.1, and 8.2) on the non‐covalent nanocomplexes' functional properties and the WP‐EGCG interactions were investigated by studying antioxidant activity, emulsification, fluorescence quenching, and molecular docking, respectively. RESULTS With the formation of non‐covalent and covalent complexes, the amide band decreased; the ‐OH peak disappeared; the antioxidant activity of WP‐EGCG non‐covalent complexes was 2.59‐ and 2.61‐times stronger than WP‐EGCG covalent conjugates for 1‐diphenyl‐2‐picryl‐hydrazyl (DPPH) and ferric reducing ability of plasma (FRAP), respectively (particle size: 137 versus 370 nm). The antioxidant activity (DPPH 27.48–44.32%, FRAP 0.47–0.63) was stronger at pH 6.2–7.1 than at pH 2.6 and pH 8.2 (DPPH 19.50% and 26.36%, FRAP 0.39 and 0.41). Emulsification was highest (emulsifying activity index 181 m2 g−1, emulsifying stability index 107%) at pH 7.1. The interaction between whey protein (WP) and EGCG was stronger under neutral and weakly acidic conditions: KSV (5.11–8.95 × 102 L mol−1) and Kq (5.11–8.95 × 1010 L mol s−1) at pH 6.2–7.1. Binding constants (pH 6.2 and pH 7.1) increased with increasing temperature. Molecular docking suggested that hydrophobic interactions played key roles at pH 6.2 and pH 7.1 (∆H > 0, ∆S > 0). Hydrogen bonding was the dominant force at pH 2.6 and pH 8.2 (∆H < 0, ∆S < 0). CONCLUSION Environmental pH impacted the binding forces of WP‐EGCG nanocomplexes. The interaction between WP and EGCG was stronger under neutral and weakly acidic conditions. Neutral and weakly acidic conditions are preferable for WP‐EGCG non‐covalent nanocomplex formation. © 2023 Society of Chemical Industry.

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