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     

Changes in lipids and proteins of marine catfish (Tachysurus dussumieri) during frozen storage

Changes in lipids and protein of marine catfish ( Tachysurus dussumieri ) were followed over a period of 300 days storage at –20°C. Phospholipids decreased and free fatty acids (FFA) and peroxide value (PV) increased. A linear relationship between the decrease in phospholipid and increase in FFA was observed, suggesting that FFA were formed by hydrolysis of phospholipid. Fatty acid analysis showed that polyunsaturated fatty acids (PUFA) increased in the neutral lipid fraction and decreased in the phospholipid fractions; this also suggests hydrolysis of the latter and release of free PUFA into the neutral fraction.
A decrease in water soluble protein (WSP) and salt soluble protein (SSP) indicated denaturation of proteins on prolonged frozen storage; both changes were strongly associated with the changes in peroxide value and free fatty acids.     

Differential lipid damage in various muscle zones of frozen hake (Merluccius merluccius)

 A comparison of the lipid damage produced in different hake zones was carried out during frozen storage at –11 and –18  °C. Three light muscle zones and the dark muscle were considered. Lipid oxidation [conjugated dienes; thiobarbituric acid index (TBA-i); fluorescence formation] and hydrolysis (free fatty acids, FFA) were determined. The most predominant lipid damage in all zones was hydrolysis, at the end of storage reaching values of about 40% (for the light muscle zones) and 12% (for the dark muscle) of the total lipids at –11  °C. Significant (P<0.05) correlation value (r=0.67–0.85) relationships between the frozen storage time and the FFA content were obtained for the four muscle zones at both temperatures. A comparison of the regression lines slopes in the different zones showed that a lower (P<0.05) lipolitic activity was produced in the dark muscle compared to the three light zones at both temperatures. A low lipid oxidation development was produced in the three light muscle parts, so that no significant differences between them could be assessed. However, the dark muscle showed a higher oxidation development (TBA-i and fluorescence formation) as a result of a higher lipid content and the presence of prooxidant constituents.     

CHANGES IN LIPIDS BOUND TO THE I-Z-I FRACTION RELATED TO THE MYOFIBRILLAR FRAGMENTATION INDEX (MFI) OF OVINE LONGISSIMUS DORSI STORED AT 4C

The lipids bound to the I‐Z‐I fraction and the Myofibrillar Fragmentation Index (MFI) of postmortem ovine Longissimus dorsi stored at 4C were investigated. At zero time of storage total lipids were composed of about 50% neutral lipid and 50% phospholipid. During storage, the neutral lipid fraction showed a significant decrease (P < 0,01) in the relative percentage of triglycerides and a significant increase (P < 0.01) in free fatty adds. The composition ofphospholipids extracted from I‐Z‐I with chloroform:methanol 2:1 (v/v) remained unchanged. Further treatment of the I‐Z‐I fraction with chloroform:methanol (2:1, v/v) containing 0.25% (v/v) of concentrated HCl extracted an additional amount of phospholipids. The content of phospholipid extractable from the I‐Z‐I fraction with acidified organic solvents significantly decreased (P < 0.01) during storage and this change was accompanied by a significant increase (P < 0.01) in the MFI.     

CONTRIBUTION OF PHOSPHOLIPIDS TO HEADSPACE VOLATILES DURING STORAGE OF PECANS

The relationship between headspace volatiles and lipid class fatty acid composition was investigated in pecans subjected to room temperature storage for 8 months. During early stages of storage, pentanal predominated in the pecan headspace, whereas at later stages hexanal predominated. Quantities of triacylglycerols recovered from pecans did not change significantly during storage, whereas a decrease in phospholipid content and an increase in free fatty acid content were seen. While losses of polyunsaturated fatty acids (PUFA) in triacylglycerols and free fatty acids only occurred during the last month of storage, PUFA losses were recorded in the phospholipid fraction by 5 months. Based on a strong negative correlation (R =?0.98) between hexanal and its precursor fatty acid (18:2) in phospholipids, the results suggested that membrane lipids would be a primary site of attack during the early stages of oxidation. Future studies with oilseeds, such as pecans, should therefore examine the possibility that variations in phospholipid fatty acid composition could explain cultivar differences in storage stability.     

Fatty acids of a salami-type sausage made of Baltic herring fillets, pork and lard

 The fatty acid composition of "fish wurst", a fermented salami-type sausage made of pork, lard and Baltic herring fillets (Clupea harengus var. membras) was investigated. Changes in the proportions of the 35 most abundant fatty acids were examined throughout the 1-month ripening period followed by a 4-month storage period. The fat composition of the product was stable (32–35%) and retained the characteristics of the main ingredients: oleic acid (37.4%, mean of three production batches) palmitic acid (23.7%) and linoleic acid (10.7%) from lard and fish, stearic acid (11.7%) mainly from lard, and palmitoleic acid (3.0%) and long-chain (C20–C24), polyunsaturated fatty acids (c.a. 6%) mainly from fish. During the 4-week ripening period a statistically significant increase (P≤0.05) was detected in the proportions of minor fatty acids only, i.e. eicosenoic acid (20 : 1n-9), eicosadienoic acid (20 : 2n-6), docosadienoic acid (22 : 2n-6) and docosatrienoic acid (22 : 3n-3). During the 4-month storage of the ripe sausage, the fatty acid composition stabilized. Only the proportion of stearic acid increased significantly during storage, from 11.7% to 12.5%. Received: 23 January 1998 / Revised version: 1 April 1998     

Differential lipid damage in various muscle zones of frozen hake (Merluccius merluccius)

 A comparison of the lipid damage produced in different hake zones was carried out during frozen storage at –11 and –18  °C. Three light muscle zones and the dark muscle were considered. Lipid oxidation [conjugated dienes; thiobarbituric acid index (TBA-i); fluorescence formation] and hydrolysis (free fatty acids, FFA) were determined. The most predominant lipid damage in all zones was hydrolysis, at the end of storage reaching values of about 40% (for the light muscle zones) and 12% (for the dark muscle) of the total lipids at –11  °C. Significant (P<0.05) correlation value (r=0.67–0.85) relationships between the frozen storage time and the FFA content were obtained for the four muscle zones at both temperatures. A comparison of the regression lines slopes in the different zones showed that a lower (P<0.05) lipolitic activity was produced in the dark muscle compared to the three light zones at both temperatures. A low lipid oxidation development was produced in the three light muscle parts, so that no significant differences between them could be assessed. However, the dark muscle showed a higher oxidation development (TBA-i and fluorescence formation) as a result of a higher lipid content and the presence of prooxidant constituents. Received: 16 June 1998     

Lipid Changes in Sea Urchin Gonads during Storage

In lipids of salted sea urchin gonads, the changes in contents of neutral lipids (NL), glycolipids (GL) and phospholipids (PL), in peroxide and carbonyl values, in lipid class compositions of NL and PL, and in fatty acid composition were investigated as a function of storage time. NL increased while GL and PL decreased by autolysis during 180 days storage. The increase of NL resulted from free fatty acids (FFA) [plus fatty acid ethyl esters (FAEE)] generated enzymatically by hydrolysis of PL and GL. Triglycerides were stable throughout a period of storage. In heat-treated and salted gonads, NL, GL and PL remained nearly unchanged during storage, and FFA and FAEE could not be detected. The oxidation of lipids was not detected during 180 days storage, although salted gonads had high content of polyunsaturated fatty acids.     

Effect of processing and storage on neutral lipids of buffalo meat

Three muscles viz. Triceps brachii (TB), Longissimus dorsi (LD) and Biceps femoris (BF) from different anatomical locations of adult male buffaloes were stored after broiling and pressure cooking under refrigerated (4°C) condition for 3, 6, 9 days and 30, 60, 90 days under frozen (-10°C) storage. At the end of each storage interval they were analysed for total lipids, cholesterol contents and glyceride fractions i.e. monoglycerides (MG), diglycerides (DG), and triglycerides (TG). Muscles differed significantly in total lipids as well as contents of all glyceride fractions. Muscle LD had significantly higher total lipid content than TB and BF. Muscles differed significantly in their esterfied cholesterol (EC) contents. Heat processing increased total lipids, cholesterol, MG, DG and TG contents of all the buffalo muscles studied. Total cholesterol contents remained unchanged during refrigerated and frozen storage. However, EC, MG, DG and TG contents declined during storage. The influence of anatomical locations on fatty acid composition of neutral lipids was observed. The ratio of unsaturated to saturated fatty acids increased due to cooking. A gradual decrease in mono- and polyunsaturated fatty acids was recorded during refrigerated and frozen storage.     

Effect of essential oils treatment on the frozen storage stability of chub mackerel fillets

The effect of bay leaf (BLO), thyme (TO), rosemary (RO), black seed (BSO), sage (SO), grape seed (GSO), flaxseed (FSO) and lemon (LO) essential oil from vegetable extracted on lipid oxidation and some other quality parameter of frozen chub mackerel during frozen storage at −20°C were examined over a period of 11 months. Taste, odour, texture and overall acceptability of control samples were given ‘unacceptable’ scores by the sixth month. Based primarily on sensory data, the shelf-lives of frozen chub mackerel were found 6 month for samples treated with oil of TO, RO, BSO, SO and LO and 7 month for samples treated with BLO, GSO and FSO. During the 11-months storing process of chub mackerel, the values of pH, total volatile basic nitrogen (TVB-N), trimethylamine nitrogen (TMA-N) both in control group samples and samples treated with oils did not reach to deterioration levels. Thiobarbitüric acid (TBA) and free fatty acid (FFA) values for all treatments remained lower than TBA and FFA values of control samples throughout the 11 month storage period. Particularly, thyme oil treatment is effective in delaying lipid oxidation. Bay leaf, rosemary, sage, lemon, flaxseed and grape seed oils were fallowed.     

Changes in lipids and their contribution to the taste of migaki-nishin (dried herring fillet) during drying

This study was conducted to investigate the changes in lipids and their effect on the taste of migaki-nishin during drying. Lipid was extracted from herring fillets following different drying stages to measure the degree of lipid oxidation and changes in lipid composition, and fatty acid profile. Peroxide value, carbonyl value and acid value of the lipids were significantly increased (P < 0.05) during the drying period. Marked increase in free fatty acids, with decreases in triglyceride and phospholipid content were observed in proportion to drying time and this result suggested that hydrolysis was induced by lipases and phospholipases. The decreases in polyunsaturated fatty acids (PUFAs), especially eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), were observed in the total lipids and phospholipid fraction. In addition, significant increase in PUFAs especially DHA was found in the free fatty acid fraction. Sensory evaluation showed that an addition of DHA to mentsuyu significantly (P < 0.05) enhances the intensities of thickness, mouthfulness and continuity. These results suggest that during drying period lipid oxidation was not only occurred but also lipolysis predominantly released DHA, which might have a contribution to kokumi enhancement of migaki-nishin.     

Changes in Fatty Acid Composition of Papaya Lipids (Carica papaya) During Ripening

Lipids from papayas (Carica papaya L.) Solo cultivar at various stages of ripeness were extracted and fractionated into neutral lipids (NL), glycolipids (GL), and phospholipids (FL). The major fatty acids of the three lipid classes at all levels of ripeness were C16:0, C18:1, C18:2, C18:3. NL increased in unsaturation with maturity as indicated in the decrease of the various saturated/unsaturated fatty acid ratios, GL decreased in the ratio of C16:0/C16:1 due to an increase in C16:1 fatty acid with increasing fruit maturity. The remaining fatty acids in GL remained relatively unchanged. The phospholipid fraction increased in unsaturation with maturity due to increases in C16:1 and C18:3 fatty acids.     

Chromatographic Column Fractionation and Fatty Acid Composition of Different Lipid Classes of Linseed Oil

Linseed oil is fractionated on silicic acid column, with subsequent identification of different lipid classes by thin layer chromatography. Sterol esters, triglycerides, free fatty acids, sterols and phospholipids represent 0.15, 92.25, 3.30, 1.15 and 1.16%, respectively of linseed lipids. The total saturated fatty acid content of the phospholipid fraction is higher than that of the oil, the triglyceride fraction and the free fatty acid fraction. Linolenic acid, which is the major fatty acid in linseed triglycerides (47.5%), makes 18.2% of the phospholipid fatty acids. Oleic acid is the major fatty acid in the phospholipid fraction (35.2%), while it constitutes 19.3% of the triglycerides fatty acids.     

Changes in lipids of whole and minced rayfish (Raja clavata) muscle during frozen storage

The effects of the storage temperature (?18 °C and ?40 °C) and the addition of butylhydroxytoluene (BHT) on the different classes of lipids (phospholipids, triacylglycerides, free fatty acids, sterols and sterol esters plus waxes) and the fatty acid composition of minced (8 and 12 mm) and whole rayfish wing muscle stored for 1 year in the frozen state were studied. The phospholipid content decreased significantly and the free fatty acid content increased significantly at both storage temperatures, but more pronounced, at ?18 °C. Significant differences were found between phospholipid and free fatty acid contents of the minced and the whole samples, which again were more pronounced at ?18 °C. A significant increase of the major fatty acids (22∶: 6n-3 and 16:0) was observed after 1 year in the frozen state. Significant differences were also obtained between the samples stored at ?18 °C and at ?40 °C; the lower the storage temperature, the higher their content. The polyunsaturated fatty acid (PUFA) content increased significantly in all the samples. Significant differences were found between the samples stored at ?18°C and at ?40°C. The lower the temperature, the higher the PUFA content. Nonsignificant differences were observed between the 8-mm and the 12-mm minced samples. Non-significant differences were found between the samples stored in the presence and in the absence of BHT. Mincing hastened hydrolytic and oxidative processes, which were slowed down at the lower storage temperature. Nonetheless, nonsignificant differences were found between both particle sizes.     

Changes in the fatty acid composition of dietetic ready-to-cook chicken meat products during frozen storage

A study was made on the fatty acid composition of dietetic ready-to-cook products of boneless chicken legs or breasts prepared by curing using several curing mixtures during frozen storage. Leg muscles were found to be richer in unsaturated fatty acids than breast muscles, substantial differences having been found in the contents of palmitoleic and linolenic acids. During frozen storage, the contents of unsaturated fatty acids were reduced, especially intensively in the leg muscle ready-to-cook products. The fastest changes occurred in linolenic and linolic acids and partly in palmitic acid. The level of oleic acid remained substantially unchanged throughout the storage period. Irrespective of the changes found, the ratio of unsaturated and saturated fatty acids in all the groups studied remained greater than 1 for both types of meat. The application of citrate in the curing mixture had a favourable effect on the changes, in that a minimum alteration in the contents of unsaturated fatty acids was achieved.     

Fatty acids of a salami-type sausage made of Baltic herring fillets, pork and lard

 The fatty acid composition of "fish wurst", a fermented salami-type sausage made of pork, lard and Baltic herring fillets (Clupea harengus var. membras) was investigated. Changes in the proportions of the 35 most abundant fatty acids were examined throughout the 1-month ripening period followed by a 4-month storage period. The fat composition of the product was stable (32–35%) and retained the characteristics of the main ingredients: oleic acid (37.4%, mean of three production batches) palmitic acid (23.7%) and linoleic acid (10.7%) from lard and fish, stearic acid (11.7%) mainly from lard, and palmitoleic acid (3.0%) and long-chain (C20–C24), polyunsaturated fatty acids (c.a. 6%) mainly from fish. During the 4-week ripening period a statistically significant increase (P≤0.05) was detected in the proportions of minor fatty acids only, i.e. eicosenoic acid (20 : 1n-9), eicosadienoic acid (20 : 2n-6), docosadienoic acid (22 : 2n-6) and docosatrienoic acid (22 : 3n-3). During the 4-month storage of the ripe sausage, the fatty acid composition stabilized. Only the proportion of stearic acid increased significantly during storage, from 11.7% to 12.5%. Received: 23 January 1998 / Revised version: 1 April 1998     

Stability of lipids and fatty acids in frozen and gamma irradiated Patagonian toothfish (Dissostichus eleginoides) from the Southwestern Atlantic

Patagonian toothfish were captured in the Southwestern Atlantic Ocean (FAO Zone N° 41). The fatty acid profile of total lipids and the triacylglycerol and phospholipid content of control and irradiated samples (1 and 5 kGy) stored at −18 °C were analyzed at 0 and 293 days post irradiation. The fatty acids are mainly monounsaturated acids (47 g/100 g total fatty acids), the most abundant one being oleic acid (18:1 n-9). This is followed in order of abundance by saturated fatty acids (26 g/100 g total fatty acids), consisting mainly of palmitic acid (16:0). Polyunsaturated fatty acids were less abundant (17 g/100 g total fatty acids) and consisted mainly of eicosapentaeonic (20:5 n-3) and docosahexaenoic (22:6 n-3) acids. Triacylglycerol content was 563.07 mg/mL oil, whereas phospholipids were 11.21 mg/mL oil. Gamma irradiation did not significantly affect the fatty acid profile or triacylglycerol and phospholipid content of P. toothfish stored for 293 days at −18 °C. The results suggest that the species exhibits a marked stability when subjected to irradiation and prolonged storage in the frozen state.     

Time-related changes in intramuscular lipids of French dry-cured ham

The aim of this study was to investigate the changes in intramuscular lipids during the processing of French dry-cured hams. In the fresh biceps femoris muscle, the lipid content was on average, 105 mg/g DM with a large individual variation. Glycerides accounted for about 75% of total lipids. During processing for 273 days, phospholipid content decreased markedly whereas free fatty acid content rose from 1·9 mg/g DM to 9·4 mg/g DM. Little change affected the fatty acid composition of both glycerides and phospholipids during processing. After a decrease in the proportion of polyunsaturated fatty acids during the first 2 months, free fatty acid composition remained stable. The results suggest that lipid alteration during dry-curing of hams is due to lipolysis and that lipid oxidation is limited.     

Fatty Acids of Neutral and Phospholipids, Rancidity Scores and TBA Values as Influenced by Packaging and Storage

The fatty acid (FA) of neutral lipids (NL) and phospholipids (PL) and this composition's relationship to rancidity score and TBA values of cooked beef patties, during frozen storage at times up to 4½ months under vacuum and nonpackaged conditions were studied. The predominant FA in the NL was C_18:1 (46.0%), followed by C_16:0 at 29.2%. However, the PL fraction gave a more balanced distribution of FA. In the neutral lipid fractions, reduction in the C_16:1 and C_18:2 fatty acids made significant contributions to increased rancidity scores and TBA values but in the phospholipid fraction, changes in the C_18:3 and C_20:4 were of greatest importance. After 3 months of frozen storage a regression model containing the neutral lipid fatty acids C_18:1 and C_18:2 and the phospholipid fatty acids C_18:3 and C_20:4 accounted for 88% and 85% of the variation in rancidity score and TBA value.     

Composition of Lipids in Some Beef Muscles

SUMMARY— The lipids extracted from five different muscles of four Angus steers were separated into phospholipids, free fatty acids, and a fraction containing the triglycerides. The phospholipid concentration for a given muscle was relatively constant in all four animals. The concentration of total lipids varied considerably more than that of phospholipids. The diaphragm had the highest total lipid and phospholipid content. The diaphragm also differed from the other muscles studied in the palmitic and steak acid concentration of the phospholipids. The free fatty acid concentration varied from muscle to muscle, however, two distinct patterns of free fatty acid distribution were observed in the four animals. The triglycerides and phospholipids differed in the qualitative composition of their fatty acids. Approximately 20% of the phospholipid fatty acids, but only a trace of triglyceride fatty acids, were above C₂₀. The phospholipids contained a much greater amount of polyunsaturated acids than the triglycerides.