2013
DOI: 10.1111/1750-3841.12044
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Compositional Characteristics of Materials Recovered from Headed Gutted Silver Carp (Hypophthalmichthys molitrix) by Isoelectric Solubilization and Precipitation Using Organic Acids

Abstract: This research presents a reliable method for extracting nutritionally valuable fish protein and oils from otherwise hard to process fish and its byproducts. Replacing the traditionally used strong acids with organic acids might further accomplish bacterial load reduction while resulting in similar to or improved protein recovery yields. Therefore, this technology may increase the commercial viability of hard to process fish.

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Cited by 13 publications
(42 citation statements)
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“…A package of vacuum‐packaged fish containing 500 g paste was thawed at 4 °C for 24 h prior to processing. The thawed paste was diluted with distilled deionized water at a 1: 6 (fish: water) ratio in a glass beaker and homogenized (PowerGen 700, Fisher Scientific, Pittsburgh, PA, USA) for 5 min . Proteins were solubilized by increasing the pH of the solution to either 11.0, 11.5, 12.0 or 12.3 with 1 mol L −1 calcium hydroxide (Ca(OH) 2 ) or 10 mol L −1 sodium hydroxide (NaOH).…”
Section: Methodsmentioning
confidence: 99%
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“…A package of vacuum‐packaged fish containing 500 g paste was thawed at 4 °C for 24 h prior to processing. The thawed paste was diluted with distilled deionized water at a 1: 6 (fish: water) ratio in a glass beaker and homogenized (PowerGen 700, Fisher Scientific, Pittsburgh, PA, USA) for 5 min . Proteins were solubilized by increasing the pH of the solution to either 11.0, 11.5, 12.0 or 12.3 with 1 mol L −1 calcium hydroxide (Ca(OH) 2 ) or 10 mol L −1 sodium hydroxide (NaOH).…”
Section: Methodsmentioning
confidence: 99%
“…The solution was homogenized for 10 min after the final pH was reached and confirmed with a calibrated pH/ion analyzer (Oakton, Eutech Instruments, Singapore). The slurry was transferred into 1 L centrifuge bottles and centrifuged at 98 066.5 m s −2 for 15 min at 4 °C (Sorvall RC‐SB refrigerated superspeed centrifuge, Du Pont, Wilmington, DE, USA) to separate the lipids and insolubles (skin, bones and scales) from the protein solution . Following centrifugation, lipids formed the top layer, protein remained solubilized in the liquid fraction and the insoluble components were at the bottom.…”
Section: Methodsmentioning
confidence: 99%
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