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- W4255773802 abstract "Using classic haem protein quantification methods, the extraction step in buffer or acid acetone often becomes limiting if muscle is oxidised and/or stored; haem-proteins then tend to bind to muscle components like myofibrils and/or biomembranes. The objective of this study was to develop a new haem protein determination method for fish muscle overcoming such extractability problems. The principle was to homogenise and heat samples in an SDS-containing phosphate buffer to dissolve major muscle components and convert ferrous/ferric haem proteins to hemichromes with a unique absorption peak at 535 nm.Hb-recovery tests with the new and classic methods showed that the new method and Hornsey’s method performed significantly better on fresh Hb-enriched cod mince than Brown’s and Drabkin’s methods; recovery was ⩾98%. However, in highly oxidised samples and in cod protein isolates made with acid pH-shift processing, the new method performed better than Hornsey’s method (63% and 87% vs. 50% and 68% recovery). Further, the new method performed well in fish muscle with ⩽30% lipid, <5% NaCl and pH 5.5–7.0; it was also unaffected by freezing/frozen storage." @default.
- W4255773802 created "2022-05-12" @default.
- W4255773802 date "2012-09-01" @default.
- W4255773802 modified "2023-09-26" @default.
- W4255773802 title "Special Issue Title page" @default.
- W4255773802 doi "https://doi.org/10.1016/s0044-8486(12)00494-2" @default.
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