High-pressure homogenization pretreatment enhances flavonoid release and bioactive peptide production in quinoa protein hydrolysates: In vitro and in silico analysis of bioactive properties
2025
Carvalho Oliveira, Ludmilla de | Peñas, Elena | Frías, Juana | Cartea González, María Elena | Francisco, Marta | Martínez-Villaluenga, Cristina | Cristianini, Marcelo | Fundação de Amparo à Pesquisa do Estado de São Paulo | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brasil) | Agencia Estatal de Investigación (España) | Ministerio de Ciencia, Innovación y Universidades (España) | European Commission
This research explored the impact of high-pressure homogenization (HPH) at 50, 100, and 180 MPa as a pretreatment for enzymatic hydrolysis of quinoa protein isolate (QPI) using Alcalase, focusing on protein solubility, protein profile, degree of hydrolysis (DH), free amino acids, total soluble phenolic compounds (TSPC), angiotensin-converting enzyme-inhibitory (ACEI) and antioxidant activities (AA), and characterization of phenolics and peptides. Pretreatment at 50 MPa (QPH50) reduced DH from 15.98 % (non-pretreated hydrolysates) to 13.53 %. The hydrolysates comprised low free amino acid levels (2.5–2.7 g/100 g). Soluble protein decreased, and SDS-PAGE confirmed globulin hydrolysis (>25 kDa) for all hydrolysate samples, with an increase in small peptides (<5 kDa). QPI hydrolysis increased TSPC and AA in methanol-acetone and aqueous extracts, reaching their highest levels at 50 MPa (aqueous extract). The 3 kDa permeates showed strong ACEI activity at 0.5 mg/mL (91.5–93.2 %), with QPH50 exhibiting the highest inhibition (92.6 %; IC50 = 0.04 mg/mL). Further characterization of QPH50 showed enhanced flavonoid content (10.1 mg/100 g). Peptidomic analysis of QPH50 identified 236 peptide sequences, 27 predicted bioactive, with SPGYYDGR and AGLQFPVGR ranking highest for multifunctional potential. This study highlights the effectiveness of combining HPH with enzymatic hydrolysis to release phenolics and bioactive peptides, with high bioavailability and promising safety profiles.
Mostrar más [+] Menos [-]This work was supported by the Sao Paulo Research Foundation (FAPESP) [grant numbers 2022/00512-0 and 2019/05578-7]; the Coordination for the Improvement of Higher Education Personnel - Brazil (CAPES) [Finance Code 001] and Grant PID2022-138978OB-I00 funded by MCIN/AEI/10.13039/501100011033 and “FEDER A way of making Europe".
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Información bibliográfica
Este registro bibliográfico ha sido proporcionado por Instituto de Ciencia y Tecnología de Alimentos y Nutrición