1995•Journal of the Science of Food and AgricultureRequires access

The effect of frozen storage of mackerel (Scomber scombrus) on its quality when hot‐smoked

Αναστάσιος Ζώτος, Michael Hole, Gillian Smith

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Abstract

Abstract Whole mackerel (Scomber scombrus) were frozen using a horizontal plate freezer, wrapped in plastic bags and frozen stored at ‐ 20°C. At suitable intervals (11, 22 and 33 weeks) the fish were removed from the cold store and subsequently hot smoked (in gutted from) using an AFOS‐Torry Mini Kiln. All smoked mackerel samples, despite their different previous histories, were assessed by the panellists as moderately acceptable products in‐ terms of their texture and flavour, even after 33 weeks frozen storage prior to smoking. Protein denaturation, as related to salt‐soluble protein, was influenced by the frozen storage history (24% drop after 33 weeks frozen storage) and seemed to be affected by the free amino acids formed during frozen storage. After smoking the denaturation was extensive (above 80%) in all mackerel samples. Lipid oxidation was quite extensive (PV 108 meq kg−1) in the 22 and 33 weeks frozen stored mackerel samples. However, no rancid flavour in the latter smoked mackerel samples was detected by taste panellists. A 58% increase in free amino acids during frozen storage was observed. Extensive losses of 74% in available lysine were observed in the 22 and 33 weeks frozen stored mackerel samples after smoking which could be due to aminocarbonyl reactions with the products of lipid oxidation. A 40% loss of thiamine was observed in the 33 weeks frozen stored samples after smoking. The histamine contents did not exceed 94 mg kg−1 and would not be expected to cause symptoms of scombrotoxin poisoning.

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What this paper is about

Abstract Whole mackerel (Scomber scombrus) were frozen using a horizontal plate freezer, wrapped in plastic bags and frozen stored at ‐ 20°C. At suitable intervals (11, 22 and 33 weeks) the fish were removed from the cold store and subsequently hot smoked (in gutted from) using an AFOS‐Torry Mini Kiln. All smoked mackerel samples, despite their different previous histories, were assessed by the panellists as moderately acceptable products in‐ terms of their texture and flavour, even after 33 weeks frozen storage prior to smoking. Protein denaturation, as related to salt‐soluble protein, was influenced by the frozen storage history (24% drop after 33 weeks frozen storage) and seemed to be affected by the free amino acids formed during frozen storage. After smoking the denaturation was extensive (above 80%) in all mackerel samples. Lipid oxidation was quite extensive (PV 108 meq kg−1) in the 22 and 33 weeks frozen stored mackerel samples. However, no rancid flavour in the latter smoked mackerel samples was detected by taste panellists. A 58% increase in free amino acids during frozen storage was observed. Extensive losses of 74% in available lysine were observed in the 22 and 33 weeks frozen stored mackerel samples after smoking which could be due to aminocarbonyl reactions with the products of lipid oxidation. A 40% loss of thiamine was observed in the 33 weeks frozen stored samples after smoking. The histamine contents did not exceed 94 mg kg−1 and would not be expected to cause symptoms of scombrotoxin poisoning.

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Available abstract

Abstract Whole mackerel (Scomber scombrus) were frozen using a horizontal plate freezer, wrapped in plastic bags and frozen stored at ‐ 20°C. At suitable intervals (11, 22 and 33 weeks) the fish were removed from the cold store and subsequently hot smoked (in gutted from) using an AFOS‐Torry Mini Kiln. All smoked mackerel samples, despite their different previous histories, were assessed by the panellists as moderately acceptable products in‐ terms of their texture and flavour, even after 33 weeks frozen storage prior to smoking. Protein denaturation, as related to salt‐soluble protein, was influenced by the frozen storage history (24% drop after 33 weeks frozen storage) and seemed to be affected by the free amino acids formed during frozen storage. After smoking the denaturation was extensive (above 80%) in all mackerel samples. Lipid oxidation was quite extensive (PV 108 meq kg−1) in the 22 and 33 weeks frozen stored mackerel samples. However, no rancid flavour in the latter smoked mackerel samples was detected by taste panellists. A 58% increase in free amino acids during frozen storage was observed. Extensive losses of 74% in available lysine were observed in the 22 and 33 weeks frozen stored mackerel samples after smoking which could be due to aminocarbonyl reactions with the products of lipid oxidation. A 40% loss of thiamine was observed in the 33 weeks frozen stored samples after smoking. The histamine contents did not exceed 94 mg kg−1 and would not be expected to cause symptoms of scombrotoxin poisoning.

Key concepts: Scomber, Mackerel, Chemistry, Food science, Smoked fish, Flavour, Congelation, Lipid oxidation

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