Evaluation of some physico-chemical properties of restructured trout and hake mince during cold gelation and chilled storage

Cold gelation was carried out on trout (Oncorhynchus mykiss) or on hake (Merluccius merluccius) mince with or without addition of fish oil and using microbial transglutaminase (MTGase). Products were stored at 4 °C for 6 days and lipid oxidation, protein oxidation, texture, water binding capacity, and colour were followed. Results indicated that MTGase was able to generate gels with good properties for both trout and hake. Gels prepared with trout were oxidised whilst gels prepared with hake were stable toward oxidation even in the presence of 5% fish oil. However, in the presence of oil, as an alternative for generating omega-3 enriched products, the activity of MTGase was impaired, as the gels took longer to reach maximum hardness. Furthermore, in all samples containing MTGase, protein oxidation was high.     

Antioxidant activity of black currant (Ribes nigrum L.) extract and its inhibitory effect on lipid and protein oxidation of pork patties during chilled storage

This experiment was conducted to assess the antioxidant efficacy of black currant (Ribes nigrum L.) extract (BCE) in raw pork patties during chilled storage. The extracting conditions of frozen BCE including ethanol concentrations (0-100%) and extracting times (0.25-12h) were studied. BCE extracted with 40% ethanol for 2h had the highest anthocyanin content, the strongest radical scavenging activities as well as the second strongest reducing power. BCE was condensed and added to pork patties at 5, 10 or 20 g/kg. Compared with the control, BCE treatments significantly decreased the thiobarbituric acid-reactive substance values and carbonyls formation and reduced the sulfhydryl loss of pork patties in a dose-dependent manner (P<0.05), which showed that the BCE significantly inhibited lipid and protein oxidation. The BCE-treated patties showed significantly higher redness (P<0.05) than the control. The findings demonstrated strong potential for BCE as a natural antioxidant in meat and meat products.     

In vitro antioxidant activity of papain‐treated grass carp (Ctenopharyngodon idellus) protein hydrolysate and the preventive effect on fish mince system

Antioxidant activities of papain‐treated grass carp protein hydrolysate (HP) were investigated using in vitro methods and in grass carp mince system. Lipid oxidation, colour changes and cooking loss in grass carp mince added with 0% (control), 0.5%, 1.0%, 2.0% and 4.0% HP during refrigerated storage (4 °C) for 8 days was studied. HP could chelate 50% of Fe²⁺ and scavenge 50% of hydroxyl radicals at the concentration of 0.81 and 8.12 mg mL^?1, respectively. And HP could effectively decrease peroxide values and inhibit the formation of thiobarbituric acid reactive substances in fish mince throughout storage (P < 0.05), at the application level range from 0.5% to 4.0%. In HP‐treated samples the formation of conjugate dienes (CDs) was retarded 5–30% at day 6 of storage compared to control. In addition, HP could significantly decrease cooking loss of fish mince samples, at the application level range from 1.0% to 4.0%.     

Comparative studies of four different phenolic compounds on in vitro antioxidative activity and the preventive effect on lipid oxidation of fish oil emulsion and fish mince

Antioxidative activities of different phenolic compounds (catechin, caffeic acid, ferulic acid and tannic acid) at various levels were determined by different assays. Among all the phenolic compounds tested, tannic acid exhibited the highest 2,2-diphenyl-1-picryl hydrazyl (DPPH) and 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging activities and ferric reducing antioxidant power (FRAP). Nevertheless, catechin showed the highest metal chelating activity (P < 0.05), whereas caffeic acid had the highest lipoxygenase (LOX) inhibitory activity (P < 0.05). The impact of different phenolic compounds at a level of 100 mg/l on lipid oxidation of menhaden oil-in-water emulsion and mackerel mince was investigated. Tannic acid showed the highest efficacy in retardation of lipid oxidation for both model systems as evidenced by the lower peroxide value (PV), conjugated diene (CD) and thiobarbituric acid-reactive substances (TBARS) values. This was also related with the lower non-heme iron content in tannic acid treated samples. Tannic acid was therefore considered as the most potential natural antioxidant for controlling oxidation of fish oil-in-water emulsion and fish mince, whereas ferulic acid seemed to possess the lowest preventive effect on lipid oxidation.     

Oxidation of lipid and protein in horse mackerel (Trachurus trachurus) mince and washed minces during processing and storage

Protein and lipid oxidation was followed during processing and storage of mince and washed minces prepared from horse mackerel (Trachurus trachurus). Briefly horse mackerel mince (M0) was washed with three volumes of water, mimicking the surimi production and different washed products were obtained: M1, M2 and M3, with one, two and three washing steps, respectively. The different products were characterised (i.e. lipid content, protein, water, iron, fatty acid profile and tocopherol content) and analysed for protein and lipid oxidation in order to investigate the impact of the washing steps on oxidation. Subsequently the different products were stored for up to 96 h at 5 °C and samples were taken out regularly for analysis. Lipid oxidation was investigated by measuring primary oxidation products (lipid hydroperoxides) and secondary oxidation products (volatiles). Protein oxidation was followed by determination of protein solubility, protein thiol groups and protein carbonyl groups using colorimetric methods as well as western blotting for protein carbonyl groups. Lipid and protein oxidation markers indicated that both lipid and protein oxidation took place during processing and the ranking for oxidation was as follows M0 < M1 < M2 ? M3 with M0 being significantly less oxidised than M3. Results indicated that washing creates an imbalance in the initial prooxidant-antioxidant equilibrium in the muscle tissue and contributes to the observed differences in the oxidative status of the four products obtained. In contrast, during storage of different products, lipid oxidation development was faster in M0 and the ranking was as follows M0 > M1 > M2 ? M3. Lipid and protein oxidation developed simultaneously in different minces during storage, but it was not possible to determine at which level these two reactions were coupled.     

The influence of superchilling and cryoprotectants on protein oxidation and structural changes in the myofibrillar proteins of common carp (Cyprinus carpio) surimi

The objective of the present study was to investigate the effects of superchilling combined with cryoprotectants (a mixture of sucrose and sorbitol, 1:1) on protein oxidation and structural changes in common carp (Cyprinus carpio) surimi. With increasing storage time, the carbonyl content of myofibrillar proteins increased from 31.4 nmol/mg of protein (0 day) to 53.4, 46.3, and 39.7 nmol/mg protein at 35 days (P < 0.05) for −1 °C superchilled, −3 °C superchilled, and −3 °C superchilled with cryoprotectants samples, respectively. The incorporation of cryoprotectants into common carp surimi was found to significantly inhibit the formation of carbonyls (P < 0.05). The protein surface hydrophobicity increased in a similar direction, and the sulfhydryl content and Ca-ATPase stability decreased (P < 0.05). Emulsifying activities, gel textural hardness, springiness, and water binding capacity were also decreased, but they exhibited significant improvements at −3 °C when combined with cryoprotectants (P < 0.05). These results suggest that superchilling treatments at −3 °C combined with cryoprotectants offer an effective approach to reducing protein oxidation in carp surimi, thereby reducing protein structural changes known to impair the texture of surimi products.     

Avocado by-products as inhibitors of color deterioration and lipid and protein oxidation in raw porcine patties subjected to chilled storage

Processing of avocados generates an important amount of by-products such as peels and seeds that are rich in bioactive substances with proven radical suppressing activities. The objective of this study was to evaluate the effectiveness of peel and seed extracts from two avocado varieties-'Hass' and 'Fuerte'-as inhibitors of lipid and protein oxidation and color deterioration of raw porcine patties during chilled storage (4 °C/15 days). Avocado extracts significantly (p<0.05) reduced the loss of redness and the increase of lightness during storage of porcine patties. 'Fuerte' extracts were more efficient at inhibiting discoloration of chilled patties than 'Hass' extracts. Patties treated with avocado extracts had significantly lower amounts of TBA-RS than control ones throughout the storage. 'Hass' avocado extracts significantly inhibited the formation of protein carbonyls in chilled patties at day 15. The present results highlight the potential usage of extracts from avocado by-products as ingredients for the production of muscle foods with enhanced quality traits.     

Oxidation in HiOx-packaged pork Longissimus muscle predisposes myofibrillar and sarcoplasmic proteins to N-nitrosamine formation in nitrite-curing solution

The effect of meat protein in situ oxidation on the formation of N-nitrosodiethylamine (NDEA) was investigated. Fresh minced pork was untreated (Con) or treated with 700 mg/kg α-tocopherol (Toc) or 300 mg/kg tea polyphenols (PPE), packaged in a HiOx atmosphere (78.8% O₂, 18.8% CO₂, 2.4% N₂), then stored at 2 ± 1 °C for up to 10 days. Crude myofibrillar (MP) or sarcoplasmic (SP) protein (20 mg/mL) extracted from stored meat was reacted with 43 μM sodium nitrite at 80 °C for 1 h. Lipid oxidation was totally inhibited in PPE pork but increased in Con and Toc samples after 10 days. There was significant protein oxidation (losses of sulfhydryls, formation of protein carbonyls) in both MP and SP in all samples during storage. However, the Con group suffered more extensive protein oxidation than Toc and PPE and produced more NDEA (P < 0.05), indicating that protein oxidation promoted nitrosation.     

响应面法优化黄芪蛋白水解工艺及其抗氧化活性研究

目的 优化黄芪蛋白水解液工艺条件,并考察其体外抗氧化活性。方法 采用响应面分析法,在单因素试验的基础上,选择温度、pH值、酶用量、酶解时间为影响因素,以DPPH 自由基清除率为指标,采用中心组合Box-Benhnken法建立数学模型,进行响应面分析。结果 黄芪水解蛋白的最佳酶解条件为酶解温度50℃、pH 3、酶用量800U/g、酶解时间8h,该条件下水解度为52.96%,DPPH清除率为80.64%,O·－2清除率为98.93%,·OH清除率为74.83%,还原能力为2.3。结论 响应面法Box-Benhnken设计可应用于黄芪蛋白水解工艺的优化和分析,且工艺稳定可靠,得到的水解蛋白具有较强的抗氧化活性。     

Analysis of tryptophan oxidation by fluorescence spectroscopy: Effect of metal-catalyzed oxidation and selected phenolic compounds

The suitability of using fluorescence spectroscopy to assess tryptophan (TRYP) depletion by quantifying the loss of natural TRYP fluorescence during metal-catalyzed oxidation (MCO) was assessed. To analyze the effect of the oxidation conditions, N-acetyl-l-tryptophanamide (NATA) solutions were oxidized in the presence of Cu²⁺ and Fe²⁺ (40 and 80 μM), with and without 0.8 mM H₂O₂. Also, the effect of selected phenolic compounds (PhC), namely, catechin, genistein, quercetin, rutin, gallic acid and chlorogenic acid (0.08, 0.8 and 8.0 μM), on TRYP MCO was studied. Oxidation systems catalyzed by Fe²⁺ had a major oxidative potential as a result of a higher amount of free radicals formed through the Fenton reaction. PhC could exert both antioxidant and pro-oxidant effects depending on their concentration, chemical structure of the PhC and the oxidation system. In general, all PhC acted as pro-oxidant agents at the highest dose. The major pro-oxidant effect was displayed by gallic and chlorogenic acid in the presence of Fe²⁺, Cu²⁺ or Cu²⁺/H₂O₂. Quercetin, rutin and gallic acid showed antioxidant effect against TRYP oxidation at low concentrations in Fe²⁺/H₂O₂ systems. Plausible mechanisms for the antioxidant and pro-oxidant effects of PhC on TRYP oxidation are discussed in the present article. The antioxidant efficiency of PhC or PhC-rich extracts must be studied before being used as functional food ingredients.     

Enantioseparation of catechin and epicatechin in plant food by chiral capillary electrophoresis

The enantiomers of catechin and epicatechin were separated by chiral capillary electrophoresis using modified cyclodextrins as chiral selectors. Various conditions for the separation system were optimized, including the pH value and the concentration of the running buffer. A baseline separation of the catechin and epicatechin enantiomers could be achieved by using 0.1 mol l⁻¹ borate buffer (pH 8.5) with 12 mmol l⁻¹ (2-hydroxypropyl)-γ-cyclodextrin as chiral selector, a fused-silica capillary with 40 cm effective length (75 μm I.D.), +18 kV applied voltage, a temperature of 20 °C and direct UV detection at 280 nm. The method was applied to different plant food samples. (+)-Catechin and (−)-epicatechin could be verified as the most common flavan-3-ols. In the case of guaraná, however, we were able to identify all four enantiomers, both (+)- and (−)-catechin and (+)- and (−)-epicatechin, as naturally occurring compounds. This finding was verified by further isolation and purification of the flavan-3-ols and subsequent LC–MS analysis. This method allows for the identification of the authenticity of guaraná through the analysis of the catechin and epicatechin enantiomers, additionally to the conventional methods like HPLC.     

Effect of grape antioxidant dietary fibre on the prevention of lipid oxidation in minced fish: Evaluation by different methodologies

The effect of grape antioxidant dietary fibre (GADF) addition to minced fish muscle (MFM) on lipid stability during frozen storage (6 months) was studied. Concentrations of 0%, 2%, and 4% GADF were added to MFM samples. Analyses were carried out immediately after preparation of samples and during and after storage at −20 °C. GADF was characterized in terms of dietary fibre, total polyphenols and antioxidant capacity, and multifunctional antioxidant assays were carried out on all the MFM samples. The addition of red grape fibre considerably delayed lipid oxidation in minced horse mackerel muscle during the first 3 months of frozen storage.     

Effect of animal (lamb) diet and meat storage on myofibrillar protein oxidation and in vitro digestibility

Effect of pasture- or concentrate-diet on myofibrillar protein oxidation and in vitro digestibility was measured in lamb meat (M. longissimus dorsi) during a refrigerated storage of 7days under gas permeable film. Protein oxidation was measured by the carbonyl content determined chemically using 2,4-dinitrophenylhydrazine (DNPH) and specific targets of oxidation were identified by immunoblotting. Carbonyl content significantly increased during storage and diet affected protein oxidation where animals fed concentrate showed higher carbonyl group levels than animals fed pasture. To evaluate effect of diet and storage time on protein digestibility, myofibrillar proteins were exposed to proteases of the digestive tract (pepsin, and a mixture of trypsin and α-chymotrypsin) in conditions of pH and temperature which mimic digestive process. The myofibrillar protein digestibility was not influenced by the diet. Storage time had no significant effect on myofibrillar protein susceptibility to pepsin while an important increase in digestibility by trypsin and α-chymotrypsin was detected during storage.     

Potato peel extract as a natural antioxidant in chilled storage of minced horse mackerel (Trachurus trachurus): Effect on lipid and protein oxidation

The present work was undertaken to examine the utilisation of potato peel, a waste material, as a source of natural antioxidants for retarding lipid and protein oxidation in minced mackerel. Mackerel mince with two different concentrations (2.4 or 4.8 g/kg) of water or ethanol extracts of potato peel and a control with no added extracts were prepared. The samples were stored at 5 °C for 96 h and the sampling was done at time points 0, 24, 48 and 96 h. The ethanol extracts, which contained high amounts of phenolic compounds, was found to be very effective in retarding lipid and protein oxidation as it resulted in low levels of peroxide value, volatiles, carbonyl compounds and protected against the loss of α-tocopherol and tryptophan and tyrosine residues. Water extracts was less efficient especially at higher concentrations, which might be due to lower phenolic content or due to the pro-oxidative nature of some of the phenolic acids/co-extracted compounds.     

绿原酸抑制猪肉肌原纤维蛋白氧化及NDEA生成的作用研究

在羟自由基氧化体系中,研究不同添加量的绿原酸对猪肉肌原纤维蛋白(MP)理化性质和亚硝基二乙胺(NDEA)生成的影响。结果表明,氧化导致羰基含量升高,疏水性增加,蛋白结构展开。添加绿原酸后,0.1~0.5 mmol/L能有效抑制羰基的生成(p<0.05),而0.8~1.0 mmol/L未能抑制羰基的生成。0.1~2.0 mmol/L的绿原酸使肌原纤维蛋白疏水性增加,内源色氨酸荧光强度降低。绿原酸对NDEA的生成具有浓度依赖性,0.1~0.8 mmol/L的绿原酸促进NDEA生成,而0.8~2.0 mmol/L的绿原酸抑制NDEA生成。结论:适量的绿原酸抑制了肌原纤维蛋白的氧化和NDEA的生成。     

Inhibition of hemoglobin-mediated lipid oxidation in washed fish muscle by cranberry components

Fractions enriched in phenolic acids (Fraction 1), anthocyanins (Fraction 2), flavonols (Fractions 3 and 4) and proanthocyanidins (Fractions 5 and 6) were prepared from cranberry powder using Sephadex LH-20 chromatography. Fractions 2, 3, 4, and 5 had nearly equivalent reactivity in the total phenolate assay employed per mg dry weight of each fraction while Fractions 1 and 6 were less reactive. The ability of cranberry fractions to scavenge 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals as well as their inhibitory effects on hemoglobin (Hb)-mediated lipid oxidation in washed cod muscle were assessed. Addition of cranberry fractions at a level of 74 μmol quercetin equivalents per kg of washed cod muscle extended the induction time of thiobarbituric acid reactive substances (TBARS) formation in the order: Fraction 1, Fraction 3, Fraction 4 > Fraction 2 > Fraction 5 > Fraction 6. This suggests that oligomeric polyphenols (e.g., proanthocyanidins) were least effective at inhibiting Hb-mediated lipid oxidation in washed cod muscle compared to the other classes of polyphenolics in cranberry. The ability of the different cranberry fractions to scavenge DPPH radicals did not reflect their relative ability to inhibit lipid oxidation in the washed cod muscle system. Quercetin was tentatively identified as a component in cranberry that was especially effective at inhibiting Hb-mediated lipid oxidation. The ability of flavonol and proanthocyanidin-enriched fractions to inhibit Hb-mediated lipid oxidation in spite of efforts to wash away the added polyphenolics prior to Hb addition indicated these classes of polyphenolics had binding affinities for insoluble components of washed cod muscle.     

Physicochemical changes of myofibrillar proteins during processing of Cantonese sausage in relation to their aggregation behaviour and in vitro digestibility

The physicochemical changes of myofibrillar proteins, especially oxidation behaviour, were measured to determine their mechanism of action on in vitro protein digestibility during Cantonese sausage processing. The results indicated that the carbonyl level significantly increased (p < 0.05) during the process. The SH group level decreased, while S–S group level increased gradually. Protein aggregation was induced by oxidation and heat treatment. Result from Fourier transform infrared (FTIR) spectroscopy confirmed protein aggregation occurred. The analysis of in vitro digestibility showed a highly significant (p < 0.05) correlation between pepsin activity and carbonyl group formation, S–S group level, protein surface hydrophobicity, D_4,3. A negative and highly significant correlation between trypsin, α-chymotrypsin activity and carbonyl group formation was measured, while no significant correlation with S–S groups, protein surface hydrophobicity, D_4,3 was observed. It indicated that not only protein oxidation and aggregation but also degradation by pepsin would influence proteolysis with trypsin and α-chymotrypsin.     

HPLC determination of ethoxyquin and its major oxidation products in fresh and stored fish meals and fish feeds

A new method was developed to determine 1,2‐dihydro‐6‐ethoxy‐2,2,4‐trimethylquinoline (EQ, ethoxyquin), 2,6‐dihydro‐2,2,4‐trimethyl‐6‐quinolone (QI) and 1,8′‐di(1,2‐dihydro‐6‐ethoxy‐2,2,4‐trimethylquinoline) (DM) in fish meals or fish feeds, QI and DM being the oxidation products of EQ. The sample was first extracted with hexane. After the removal of hexane the three analytes were extracted from the resulting oil with acetonitrile and determined by C₁₈ reverse phase high‐performance liquid chromatography with a UV detector set at λ = 280 nm. The mobile phase was acetonitrile–0.01 M ammonium acetate (80:20 v/v). The recoveries for EQ, QI and DM from the samples spiked at different levels varied in the ranges 90–100 per cent, 75–85 per cent and 90–100 per cent respectively. At room temperature, QI and DM were the major oxidation products of EQ in stored fish meals and fish feeds. Loss of EQ from fish meals is faster than that from feeds, resulting in relatively higher accumulations of QI and DM in the fish meals. Both QI and DM, especially the former, were not stable during storage of either and could be further oxidised to unidentified compounds. The residue levels of these two compounds were thus unpredictable during storage intervals. When the storage temperature was increased to 50 °C, EQ disappeared more rapidly, but neither QI nor DM accumulated. © 2000 Society of Chemical Industry     

Functional and nutritional characteristics of proteins and lipids recovered by isoelectric processing of fish by-products and low-value fish: A review

Several fisheries are over-exploited and may collapse; yet the amounts of fish processing by-products containing muscle proteins and ω-3-rich oil are staggering. The by-products are land-filled, ground and discarded or otherwise diverted from human consumption. Due to the lack of technology to recover proteins and lipids from by-products or low-value species, this tremendous resource is unavailable for human consumption. Isoelectric solubilisation/precipitation (ISP) allows efficient recovery of fish proteins and oil which retain functionality and nutritional value of food products. Isoelectric point (pI) is a pH where protein maintains zero electrostatic charge. At pI, protein–protein hydrophobic attraction overcomes protein–water electrostatic attraction resulting in isoelectric precipitation. Conversely, isoelectric solubilisation occurs at a pH different from pI, whereby protein–water attraction and protein–protein electrostatic repulsion are favoured. Therefore, protein solubility/insolubility is induced by ISP, respectively. Consequently, ISP allows selective protein recovery. Lipids are also recovered during ISP processing. This article reviews recent ISP developments to recover proteins and lipids from by-products and low-value marine species.     

The combined effect of antioxidants and modified atmosphere packaging on protein and lipid oxidation in beef patties during chill storage

Effect of rosemary extract and ascorbate/citrate (1:1) in combination with modified atmosphere packaging (100% N(2), 80% O(2)/20% N(2)) on protein and lipid oxidation in minced beef patties during storage in the dark for up to 6 days at 4°C was investigated. A high level of oxygen in the packaging atmosphere was found to increase both lipid and protein oxidation during storage as evaluated by TBARS analysis of secondary lipid oxidation products and by 2,4-dinitrophenylhydrazine derivatization of protein carbonyls. Both antioxidant systems tested were found to inhibit lipid oxidation but not protein oxidation. In contrast, ascorbate/citrate was found to promote protein oxidation. Rosemary extract was found to regenerate or protect α-tocopherol whereas the packaging atmospheres had no effect on α-tocopherol stability. In high oxygen atmospheres both antioxidants protected the fresh red meat colour with ascorbate/citrate being more efficient than the rosemary extract, whereas no effect of antioxidant on meat colour was found in beef patties stored in 100% nitrogen.