Antioxidative peptides derived from enzyme hydrolysis of bone collagen after microwave assisted acid pre-treatment and nitrogen protection.

Int J Mol Sci

School of Food Science and Technology, Jiangnan University, Wuxi 214122, China; E-Mails: (Y.-J.L.); (J.-Y.W.); (Y.-X.L.).

Published: November 2010

AI Article Synopsis

  • - The study explored creating antioxidant peptides through enzymatic hydrolysis of bone collagen, utilizing microwave-assisted acid pre-treatment and nitrogen protection.
  • - Phosphoric acid was identified as the most effective hydrolyzing agent, achieving a highest degree of hydrolysis (9.5%) under specific conditions involving microwave intensity and time.
  • - The use of neutral proteinase yielded better results than other proteases, with optimal conditions determined, and the antioxidant capacity peaked at 3 hours of hydrolysis before declining.

Article Abstract

This study focused on the preparation method of antioxidant peptides by enzymatic hydrolysis of bone collagen after microwave assisted acid pre-treatment and nitrogen protection. Phosphoric acid showed the highest ability of hydrolysis among the four other acids tested (hydrochloric acid, sulfuric acid and/or citric acid). The highest degree of hydrolysis (DH) was 9.5% using 4 mol/L phosphoric acid with a ratio of 1:6 under a microwave intensity of 510 W for 240 s. Neutral proteinase gave higher DH among the four protease tested (Acid protease, neutral protease, Alcalase and papain), with an optimum condition of: (1) ratio of enzyme and substrate, 4760 U/g; (2) concentration of substrate, 4%; (3) reaction temperature, 55 °C and (4) pH 7.0. At 4 h, DH increased significantly (P < 0.01) under nitrogen protection compared with normal microwave assisted acid pre-treatment hydrolysis conditions. The antioxidant ability of the hydrolysate increased and reached its maximum value at 3 h; however DH decreased dramatically after 3 h. Microwave assisted acid pre-treatment and nitrogen protection could be a quick preparatory method for hydrolyzing bone collagen.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000083PMC
http://dx.doi.org/10.3390/ijms11114297DOI Listing

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