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Xanthine Oxidase Inhibitory Peptide from Distiller’s Grains: Virtual Screening and Uric Acid-Lowering Effect
Food Science 2025, 46(24): 200-207
Published: 25 December 2025
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Objective

To achieve high-value utilization of distiller’s grains, this study explored xanthine oxidase (XOD) inhibitory peptides from distiller’s grains and determined their anti-hyperuricemic effect in mice.

Methods

Potential XOD inhibitory peptides from an enzymatic hydrolysate of distiller’s grains were isolated by ultrafiltration and identified by liquid chromatography-mass spectrometry (LC-MS) and in silico analysis. The action mechanism of XOD inhibitory peptides was elucidated using molecular docking, and the anti-hyperuricemic effect in mice was evaluated.

Results

The < 1 kDa fraction exhibited the highest XOD inhibitory activity. Four XOD inhibitory peptides were obtained, namely WDLPF, WPQ, WFPE, and LQKW. Among them, LQKW demonstrated the highest activity, with a half maximal inhibitory concentration (IC50) of 2.70 mg/mL. After gastrointestinal digestion, (61.84 ± 0.82)% of its activity remained. Molecular docking revealed that LQKW primarily bound to the receptor protein 1FIQ through hydrogen bonds and hydrophobic interactions. Compared with the model group, low-, medium-, and high-dose (200, 400, and 800 mg/kg) LQKW significantly (P < 0.01) reduced serum uric acid levels by 32.59%, 35.96%, and 37.28%, respectively. Additionally, medium- and high-dose LQKW significantly (P < 0.01) decreased kidney index, creatinine, and blood urea nitrogen levels while markedly alleviating renal pathological damage in hyperuricemic mice.

Conclusion

The distiller’s grain-derived XOD inhibitory peptide LQKW exerts its inhibitory activity by binding to 1FIQ via hydrogen bonds and hydrophobic interactions, thereby effectively reducing serum uric acid levels in HUA mice and providing renal protection. This study provides theoretical support for the development of anti-hyperuricemic peptides from distiller’s grains.

Open Access Issue
Preparation of Heat-Resistant Peptides from Hongqu Rice Distiller’s Grains and Its Effect on the Thermally Induced Oxidative Tolerance in Saccharomyces cerevisiae
Food Science 2024, 45(19): 49-56
Published: 15 October 2024
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Thermally resistant peptides were obtained from enzymatical hydrolysis of Hongqu rice distiller’s grains and evaluated for its effect on resistance to thermally induced oxidative stress in Saccharomyces cerevisiae. Various proteases were screened for the survival rate of S. cerevisiae under heat stress. The enzymatic hydrolysis conditions were optimized based on the yield of thermally resistant peptides, and the peptides were identified by mass spectroscopy and its antioxidant activity was investigated. The expression of genes in the pentose phosphate pathway and the contents of intracellular coenzyme, glutathione (GSH) and reactive oxygen species (ROS) were analyzed to explore the protective effects of the peptides on S. cerevisiae from heat-induced oxidative stress. The results indicated that the optimal enzymatic hydrolysis conditions were as follows: Hongqu rice distiller’s grains/water ratio 1:10, hydrolysis temperature 50 ℃, hydrolysis time 3 h, protamex dosage 3000 U/g, and pH 8.5. Under these conditions, the yield of thermally resistant peptides was 62.44%, and the survival rate of S. cerevisiae in the presence of the prepared peptides under heat stress was 73.97%, which was 22.76% higher than that of the control group (pure water). Sequence identification showed that 16 out of the top 20 most abundant peptides had hydrophobic amino acid contents of over 50%. The peptides exhibited 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) cation radical scavenging activity with a half-maximal effective concentration (EC50) of 4.53 and 1.82 mg/mL, respectively, indicating good antioxidant activity. Besides, the thermally resistant peptides upregulated gene expression in the pentose phosphate pathway, elevated NADH kinase activity, increased GSH content by 5.74 times, and restored intracellular ROS to almost the same level as before heat stress treatment, thus enhancing resistance to heat-induced oxidative stress in S. cerevisiae.

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