Simultaneous lipolytic and oxidative changes in turkey meat stored at different temperatures

Samples from turkey breast and thigh muscle were taken from freshly slaughtered birds under sterile conditions and stored at 37, 4 or ?18°C for up to 24 months. Changes in lipid fractions, fatty acids compositions and oxidised products were determined at intervals. Lipolysis of phospholipids was observed at 37 and at 4°C and to a small extent at ?18°C, with little change in triglyceride levels. Free fatty acid levels in general increased as phospholipids decreased. Oxodienes and conjugable oxidation products increased with time of storage, the latter products being negatively correlated with phospholipid concentrations. Changes in the ratio of tetraene to triene conjugated oxidation products formed indicated that some preferential oxidation of fatty acids more unsaturated than linoleic acid was occurring initially and this was followed by an increase in the proportion of dienes being oxidised. Both lipolysis and oxidation were faster in thigh than in breast muscle (P < 0.01) in the stored meat and in in-vitro systems. It is concluded that lipolysis and oxidation interact in the degradation of lipids during storage of turkey meat.     

Lipid changes during long-term storage of canned tuna (Thunnus alalunga)

 Lipid damage during prolonged storage of canned fish was studied. Albacore tuna was processed under two sterilization conditions (115°C, 74 min; 120°C, 40 min) and then stored for up to 6 years. Analyses (lipid oxidation and hydrolysis, browning and formation of fluorescent compounds) of the lipids extracted from the white muscle of the fish and the packing oils were carried out. Muscle lipids were partially extracted by the packing oil, so that an increase in the storage time produced higher levels of free fatty acids, browning and fluorescence development in the packing oils. As regards the types of muscle, little difference between them throughout the canned storage was detected. Received: 17 February 1997 / Revised version: 12 May 1997     

Effect of frozen storage on lipids and lipolytic activities in the longissimus dorsi muscle of the pig

 Samples of longissimus dorsi muscle from pigs were vacuum-packed and stored at –18  °C for a 6-month period. The quantity of total lipids, non-polar lipids, phospholipids and cholesterol remained unchanged during storage. However, there was a decrease (1.4%) in the polyunsaturated fatty acid percentage of the phospholipid fraction after 6 months of frozen storage, mainly due to the decrease in linoleic fatty acid. Nevertheless, there was no change in fatty acid composition of the non-polar lipid fraction. Phosphatidylethanolamine was the phospholipid most affected during the frozen storage, with a significant decrease from an intial percentage of 26.6% to 23.0% after 6 months of storage. Important activities of muscle lipolytic enzymes were still recovered after the storage, which explains the continuous release of free fatty acids reported during the process, with a net increase of 50.6 mg/100 g dry matter. The highest release of free fatty acids was reported during the 1st month of frozen storage. At the 6th month of frozen storage the compositions of both the free fatty acid and phospholipid fractions were similar. With respect to oxidation, the thiobarbituric acid test number showed a slight increase during the process while the peroxide value remained unchanged. Received: 16 March 1998 / Revised version: 17 June 1998     

Effect of frozen storage on lipids and lipolytic activities in the longissimus dorsi muscle of the pig

 Samples of longissimus dorsi muscle from pigs were vacuum-packed and stored at –18  °C for a 6-month period. The quantity of total lipids, non-polar lipids, phospholipids and cholesterol remained unchanged during storage. However, there was a decrease (1.4%) in the polyunsaturated fatty acid percentage of the phospholipid fraction after 6 months of frozen storage, mainly due to the decrease in linoleic fatty acid. Nevertheless, there was no change in fatty acid composition of the non-polar lipid fraction. Phosphatidylethanolamine was the phospholipid most affected during the frozen storage, with a significant decrease from an intial percentage of 26.6% to 23.0% after 6 months of storage. Important activities of muscle lipolytic enzymes were still recovered after the storage, which explains the continuous release of free fatty acids reported during the process, with a net increase of 50.6 mg/100 g dry matter. The highest release of free fatty acids was reported during the 1st month of frozen storage. At the 6th month of frozen storage the compositions of both the free fatty acid and phospholipid fractions were similar. With respect to oxidation, the thiobarbituric acid test number showed a slight increase during the process while the peroxide value remained unchanged.     

Fatty acid composition, antioxidants and lipid oxidation in chicken breasts from different production regimes

Chicken breast from nine products and from the following production regimes: conventional (chilled and frozen), organic and free range, were analysed for fatty acid composition of total lipids, preventative and chain breaking antioxidant contents and lipid oxidation during 5 days of sub‐ambient storage following purchase. Total lipids were extracted with an optimal amount of a cold chloroform methanol solvent. Lipid compositions varied, but there were differences between conventional and organic products in their contents of total polyunsaturated fatty acids and n‐3 and n‐6 fatty acids and n‐6:n‐3 ratio. Of the antioxidants, α‐tocopherol content was inversely correlated with lipid oxidation. The antioxidant enzyme activities of catalase, glutathione peroxidase and glutathione reductase varied between products. Modelling with partial least squares regression showed no overall relationship between total antioxidants and lipid data, but certain individual antioxidants showed a relationship with specific lipid fractions.     

Influence of fatty acid composition on chemical changes in blends of sunflower oils during thermoxidation and frying

The influence of fatty acid composition on formation of new compounds at frying temperatures has been studied in seven samples of sunflower oils widely differing in their fatty acid composition. Thermal oxidation assays as well as frying experiments were carried out and samples were evaluated by measuring the new compounds formed, i.e. polymers, polar compounds and their distribution by molecular weight, and polar fatty acids and their distribution by molecular weight. The levels of all the new compounds analysed strongly depended on the degree of oil unsaturation; the two least unsaturated oils with low content of linoleic acid and high content of palmitic acid behaved exceptionally well. When considering polar compounds or polar fatty acids, the polymers/oxidised monomers ratio increased significantly as the level of degradation increased. The new compounds formed are practically identical when analysed in the used frying oils or in the lipids extracted from the counterpart fried potatoes, independently of the level of degradation.     

Influence of the oxidative quality of dietary oil on broiler meat storage stability

Broilers were fed a high fat diet containing 11% oil (9% rapeseed oil, 2% soya bean oil) and the oil was given either as fresh (peroxide value of 1 meqv. O₂kg⁻¹ oil) or as highly oxidised (peroxide value of 156 meqv. O₂kg⁻¹ oil). Diets were supplemented with 46 mg all-rac--tocopheryl acetate kg⁻¹ diet, resulting in a tocopherol content of 80.8 mg -tocopherol and 58.6 mg γ-tocopherol per kg diet in the fresh oil diet and of 44.0 mg -tocopherol and 18.3 mg γ-tocopherol per kg diet in the oxidised oil diet, respectively, reflecting the degradation of the natural occurring tocopherols in the oxidised diet. Only minor differences were seen with respect to fatty acid composition in muscles from birds fed the two diets. The oxidation of the dietary oil lowered lipid stability significantly (p < 0.01) in both raw and precooked meats during chill storage, whereas only minor effects on the stability of frozen meat were seen. Tocopherol levels were significantly lower (p < 0.01) in muscles from birds fed the oxidised oil diet, explaining the decreased lipid stability of meat from these birds. Thigh meat was more susceptible to lipid oxidation during storage than breast meat, regardless of dietary treatment, although thigh meat had markedly higher tocopherol levels than breast meat. The molar ratio of PUFA > 18:2 (polyunsaturated fatty acids with three or more double bonds) to -tocopherol was significantly (p < 0.01) higher in thigh meat compared with breast meat, explaining the lower stability of the former during storage.     

Evolution of available lysine and lactose contents in supplemented microencapsulated fish oil infant formula powder during storage

In this work we report the evolution of available lysine, lactose and lipid hydroperoxide contents as indicators of food quality and stability of two types of infant formula powder stored at 25° and 37 °C for 12 months. The first type was supplemented with microencapsulated fish oil (MFO), made of little powder particles in a food starch‐coated matrix of caseinate and saccharose to prevent the oxidation of polyunsaturated fatty acid (PUFA). The second type was not supplemented and was used for reference. MFO might not be stable during storage and affect negatively the quality of the formula in two ways: by oxidation of PUFA, which may also easily react with lysine upon oxidation, blocking lysine, or by hydrolysis of saccharose, producing reducing sugars and increasing the Maillard reaction. Slight changes were observed in lysine and lactose evolution. By comparing the two formulae, this study shows that the MFO material did not negatively affect the studied parameters, indicating therefore acceptable stability in the conditions tested.     

Oxidative changes during ice storage of rainbow trout (Oncorhynchus mykiss) fed different ratios of marine and vegetable feed ingredients

Recently fish meal and oil have increasingly been replaced with proteins and oils from vegetable sources in the diets of farmed salmonids, but the consequences for the oxidative stability of the resulting fish products have not been investigated. The aim of the present study was to evaluate the influence of feeding regime on composition of rainbow trout fillets, as well as on lipid and protein oxidation during storage on ice. Rainbow trout were fed six different diets, which differed in their levels of marine oil and proteins vs. vegetable oil and protein. Fish fillets were characterised by measurement of fatty acid and amino acid composition, primary and secondary lipid oxidation products, astaxanthin and tocopherol content. Protein oxidation was assessed by measuring protein carbonyl content, oxidised amino acids, sulfhydryl groups and immuno-blotting against carbonyl groups. Feeding regimes significantly influenced fatty acid composition. Replacement of fish oil with vegetable oil reduced formation of primary oxidation products, but the effect on secondary oxidation products differed between different types of volatiles. The differences in protein and amino acid composition were not significant, and there were no clear effects of diets on protein oxidation, but data indicated that compounds present in the marine ingredients might have had an effect on protein oxidation.     

Lipolysis and Oxidation in Ultra‐High Temperature Milk Depend on Sampling Month,Storage Duration,and Temperature

During storage, some factors (for example, storage duration and temperature) can affect milk stability and consumer acceptability. Thiobarbituric acid reactive substances (TBARSs), lipid classes, and fatty acid profiles in stored ultra‐high temperature (UHT) milk were analyzed to assess the effects of storage time and temperature on lipid oxidation and lipolysis. With storage duration up to 12 months, the milk fat phase was separated and showed high levels of oxidation and lipolysis, manifested as increased levels of TBARS and free fatty acids. High oxidation levels decreased the percentage of unsaturated fatty acids (UFAs) in triacylglycerol and phospholipids. Higher storage temperatures (20, 30, and 37 °C) resulted in a higher degree of fat aggregation, oxidation, and lipolysis compared with refrigerated storage (4 °C). Additionally, sampling month of raw milk (May, July, and November) affected the lipid profiles of UHT milk during storage, with more UFA oxidized in July than in the other 2 months.     

Effects of Oxygen Absorber and Temperature on ω3 Polyunsaturated Fatty Acids of Sardine Oil during Storage

To prevent loss of w3 polyunsaturated fatty acids over long-term preservation, the effects of temperature and oxygen absorber on the fatty acids of sardine oil stored in air-tight film were studied. The fatty acids of sardine oil and lipids in the diet of experimental animals rapidly decreased over 1 month at 22°C. The amounts in the diet decreased slowly at 2°C; however, no alterations in the oil samples were observed for 6 months. Also, the amounts did not change at -30°C. Significant changes in samples treated with oxygen absorber were not observed under all temperatures during 6 months storage (P > 0.05). These results indicate that treatment with an oxygen absorber and/or freezing can prevent ω3 polyunsaturated fatty acids of fish oil from decreasing during storage.     

Partitioning of organic chemicals to storage lipids: elucidating the dependence on Fatty Acid composition and temperature

Lipids serve as important compartments in partitioning of neutral organic chemicals into organisms. Storage lipids, made up of triglycerides with various fatty acids, are among the major classes of lipids. Here, we present experimental equilibrium partition data for diverse chemicals in fish oil, linseed oil, and goose fat at 37 °C. These data, in combination with data from the literature for olive oil and milk fat, show that the fatty acid composition of triglycerides has no significant influence on the partition coefficient. This result allows the derivation of a general predictive model for partitioning into storage lipids. We have collected storage lipid/water partition coefficients for 247 compounds to calibrate polyparameter linear free energy relationships (pp-LFERs) for 37 °C, which achieved a model fit with a root mean squared error of 0.20 log units. To extend the applicability of this model toward the aquatic food chain, we also measured fish oil partition data at 7 °C. The resulting enthalpies were used to calibrate an additional pp-LFER for the temperature dependence of storage lipid/water partitioning. This model allows us to estimate partition coefficients at desired temperatures that occur under typical ambient conditions.     

Development of a spectroscopic method to determine the content of free radical scavenging compounds and oxidation products in thermally oxidised oils

A simple spectroscopic method using 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) was developed to simultaneously monitor the contents of free radical scavenging antioxidants (FRSs) and oxidised lipid products during oxidation through selection of proper solvents. Validation of the DPPH method was conducted in a stripped oil matrix, and practical applicability of the method was tested with heated oils. The absorbance of DPPH in isooctane simultaneously reflected the changing amounts of both FRSs and oxidised lipid products, whereas the absorbance in methanol mainly reflected changes in FRSs. Total polar materials (TPMs) were found to be representative of oxidised lipid products, which reacted with DPPH in isooctane better than in methanol. Validation parameters including accuracy, precision, linearity, limit of detection and limit of quantification were determined using α‐tocopherol as a model for FRSs and TPMs for oxidised lipid products. The DPPH protocol in isooctane and in methanol is useful for assessing the degree of oxidation in heated oils through comparing the contents of FRSs and oxidised lipids.     

Quality of Crude Fish Oil Extracted from Herring Byproducts of Varying States of Freshness

ABSTRACT: Herring byproducts were stored at 2 and 15 °C for up to 72 h. Over time, significant increases of total volatile bases (TVB), histamine, putrescine, cadaverine, and tyramine were detected. However, only tyramine and TVB levels were temperature-dependent. The level of total polyunsaturated fatty acids (PUFAs) was constant. Longer byproducts storage gave rise to an oil with higher levels of free fatty acids, eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), and total PUFAs, while fluorescent compounds were lower. A higher storage temperature led to oil higher in α-tocopherol and EPA levels and lower in anisidine value. Surprisingly, the oil with the highest content of PUFAs was not produced from the freshest byproducts, and oil with low oxidation products can be extracted from stored byproducts.     

Tocopherol content,peroxide value and sensory attributes in roasted peanuts during storage

The objective of this study was to determine changes in tocopherol content, peroxide value (PV) and sensory attributes from roasted peanuts during storage at 40 °C. There were no differences in tocopherol contents between roasted and raw peanuts except in α‐tocopherol content that decreased after roasting. All tocopherol contents decreased during storage. On the contrary, lipid oxidation indicators such as PV and the intensity ratings of oxidised and cardboard flavour increased during storage. On the other hand, the intensity ratings of roasted peanutty flavour decreased with storage time. Good correlations were observed between tocopherol contents and PVs. Tocopherol contents could be used as indicator of oxidative state in peanut products.     

Stability of Crude Herring Oil Produced from Fresh Byproducts: Influence of Temperature during Storage

ABSTRACT: Crude herring oil, extracted from fresh byproducts, was stored at 0, 20, and 50°C in order to study the effect of temperature on lipid oxidation. The oil had an initial peroxide value (PV), anisidine value (AV), and free fatty acids of 0.7 meq peroxides/kg of lipid, 0.4, and 0.6%, respectively. During storage, the oil reached the secondary oxidation stage for all 3 temperatures. The formation of fluorescent compounds was inhibited at 0°C. Significant decrease of the α-tocopherol content was found after storage at 0 and 20°C, but no consumption occurred at 50°C. The development of oxidation products over time exhibited a temperature-dependency with a very good correlation.     

Phospholipids of marine origin. III.—The pilchard (Sardina ocellata,Jenyns) with particular reference to oxidation in pilchard meal manufacture

The progress of the oxidation of phospholipids and non-phosphorylated lipids in the manufacturing process of pilchard meal was examined. It was shown that pilchard phospholipids were oxidised to a certain extent in the laboratory drying process, but a severe destruction of phospholipid and non-phosphorylated lipid fatty acids took place on storage of the meal at room temperature. Phospholipid oxidation was determined by the drop in average unsaturation of the fatty acids and also by the drop in free amino-nitrogen. In addition, the composition of pilchard phospholipids was determined.     

Effect of the addition of air-classified barley flours on the lipid stability of bakery products

Whole grains are a potential source of dietary antioxidants, and their phenolic compounds play a potential role in the prevention of lipid oxidation. In the present study, the barley coarse fraction was tested as a source of phenolic compounds to minimize lipid oxidation in bakery products (tarallini) during storage. The content of phenolic compounds in wheat and barley flours and in their mixtures was evaluated by capillary electrophoresis. Three recipes of tarallini were formulated containing different levels of barley coarse fraction (0, 20, 50%, w/w) and either extravirgin olive oil or sunflower oil. Samples were stored for 6 months and analysed every 3 months. The peroxide value was used to establish the primary oxidation state; secondary oxidation products were also evaluated (oxidized fatty acid and diene and triene conjugated by UV). All samples showed an increase in lipid oxidation during storage. The increase in peroxide values after 6 months was in the range of 183–574%. Tarallini prepared with sunflower oil showed the highest lipid oxidation. Antioxidant effects were not observed with the coarse fraction phenolic compounds.     

草鱼片热风干制过程中脂质氧化特性研究

探讨热风干燥过程中青鱼片油脂的变化情况。在青鱼片的不同干燥阶段提取油脂,检测油脂氧化程度,油脂成分及脂肪酸组成的含量变化。在干燥过程中鱼片油脂的过氧化值、羰基价和酸价显著性升高(P<0.05)。随着甘油三酯和磷脂含量的下降,游离脂肪酸含量明显增加,表明在干制过程中油脂在酯酶和磷酸化酶的催化下发生了水解反应。在总油脂和总磷脂中多不饱和脂肪酸,尤其是二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)含量下降。在游离脂肪酸中,除DHA以外的多不饱和脂肪酸含量均显著升高。研究结果表明,青鱼片热风干燥过程中其油脂被氧化,同时发生脂质降解,特别是不饱和脂肪酸被释放为游离态。     

Stability of Ethanol-Extracted Brown Rice to Hydrolytic and Oxidative Deterioration

Brown rice kernels extracted with EtOH at 7°C for 60 min were the most stable to lipolytic hydrolysis; free fatty acids (FFA) level in these kernels increased from 1.0–1.4% during 6 mo storage at 36°C. At lower extraction temperatures and times, kernels were less stable to lipolytic hydrolysis. The higher the temperature of extraction, the more susceptible kernels were to oxidative deterioration during storage; extraction time was not a factor. Kernels extracted with recycled EtOH were no more susceptible to oxidation than those extracted with fresh EtOH.