Abstract

Pretreatments with different chemicals at different concentrations to remove Ca compounds were studied to determine their effects on gelatin extraction from silver carp (Hypophthalmichthys molitrix) scales. During Ca removal with HCl, citric acid, and EDTA, all 3 chemicals were able to decalcify (>90%) scales; however, protein losses with EDTA were lower than with HCl and citric acid (P < 0.05), and protein losses with citric acid were lower than with HCl (P < 0.05). Ca removal with HCl yielded a solution where 4% to 5% of the protein was Hyp, with estimated gelatin losses from 0.9% to 2.5%. After 0.20 mol/L HCl was used for Ca removal, the extracted gelatin solution was 15.4% of the initial scales weight and gave a gel strength of 128 g. After using 1.2 g/L citric acid for Ca removal, the extracted gelatin solution was only 9% of the scales and the gel strength was 97 g. Using 0.20 mol/L EDTA for Ca removal gave a yield of 22% and a gel strength of 152 g. These data suggest that EDTA at 0.20 mol/L provides the best Ca removal with minimal collagen/gelatin removal (estimated gelatin loss was less than 0.013%) during the Ca removal step, and subsequently gave a high gelatin yield and gel strength. Fish gelatin has generally been extracted from fish skins and occasionally fish bones. This article focuses on removing the Ca compounds in fish scales and then producing fish gelatin with a good gel strength and yield. With further studies, this study may help the fish industry to have a new source of fish gelatin for food and pharmaceutical applications.

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