SPECIFICITY OF LIPOLYSIS DURING DRY SAUSAGE RIPENING

The amounts of total and individual fatty acids present in tri-glycerides (TG), free fatty acids (FFA), diglycerides (DG), monoglycerides (MG) and polar lipids (PL) were determined at various stages of dry sausage ripening using a combination of thin layer and gas chromatography. Total FFA increased from 1 to 5% of total fatty acids and DG fatty acids from 0.5 to 4%, whereas TG fatty acids showed a corresponding decrease. The rate of liberation of FFA was in the order 18:2 > 18:1 > 18:0 > 16:0 while MG and DG were enriched in 16:0. These results suggest specificity of lipolysis.     

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.     

Lipolytic and oxidative changes in Iberian dry-cured loin

This study was conducted using 61 Iberian pigs from four different genetic lines fattened under two different rearing systems. Fatty acid composition of neutral lipids (NL), polar lipids (PL) and free fatty acids (FFA) of the 61 fresh loins and their corresponding dry-cured loins and indices of lipid oxidation (hexanal, TBARS and rancid flavour) of the dry-cured loins were analyzed. Although the total amount of fatty acids from PL decreased most (89.77%), the fatty acid profile of FFA from dry-cured loin was more similar to that of NL from fresh loins. Monounsaturated fatty acids (MUFA) were the most abundant FFA type (260mg/100g muscle dry matter) followed by saturated fatty acid (SFA) (256mg/100g muscle dry matter) and polyunsaturated fatty acids (PUFA) (148mg/100g muscle dry matter). Neither genetic line nor rearing system showed any significant (P>0.05) effect on the decrease of fatty acids in the lipid fractions studied. The important decrease in PUFA from NL (43.70%) and PL (89%) was not reflected in higher oxidative indices in dry-cured loin. Neither PCA nor Pearson's correlation showed any clear relationships between lipolytic changes and oxidative indices.     

Analysis of lipid classes and the fatty acid composition of the salted fish roe food products,Ikura, Tarako,Tobiko and Kazunoko

This study was designed to clarify the content of lipid classes and the fatty acid composition of total lipids (TL), sterol esters (SE), triacylglycerols (TG), phospholipids (PL), phosphatidylcholine (PC), and phosphatidylethanolamine (PE) of the Japanese fish roe products, Ikura, Tarako, Tobiko and Kazunoko. The TL, total cholesterol, TG, and PL content of Ikura were higher than those of Tarako, Tobiko and Kazunoko. Kazunoko had the lowest cholesterol content among these roe products. PC was the main component in the PL class of each fish roe product. The main fatty acids of all roe products were 16:0, 18:1n−9, 20:5n−3, and 22:6n−3. Docosahexaenoic acid (22:6n−3) was rich in the TL, SE, TG, PL, PC and PE fractions of all roe products. In particulars the 22:6n−3 percentage of PC and PE fractions in Tobiko were higher than those of Ikura, Tarako and Kazunoko. These results indicate that the lipid from fish roe products may be a useful food source for maintaining human health.     

Effect of nitrate and nitrite curing salts on lipolysis in dry sausages produced using a rapid fermentation process

 The effect of nitrite and nitrate curing salts on lipolysis in a typical non-smoked Spanish sausage (salchichón), manufactured using a rapid dry fermentation process, was studied. From the results obtained, one could deduce that nitrite and nitrate per se do not affect the endogenous hydrolysis of the lipids during the rapid fermentation process used to produce dry sausage. Polyunsaturated fatty acids (PUFA) are liberated in greater quantities than monounsaturated (MUFA) and saturated (SFA) ones, which suggests that they are derived mainly from phospholipids. The samples that contained nitrate curing salts contained more free fatty acids (FFA) (548 mg/100 g) than those that contained nitrite curing salts (478 mg/100 g) at the end of the fermentation step, as a consequence of having undergone a preripening stage, during which significant amounts of FFA are formed. However, at the end of the ripening process, although there is a significant increase of FFA levels in all the sausages, no significant differences between samples with nitrite and those with nitrate could be found. This result could have occurred if the oxidative effects of the samples with nitrate balanced the antioxidative properties of nitrite, such that, through different processes, similar concentrations of FFA are obtained at the end of ripening. Phospholipids (PL) and free fatty acids (FFA) are the lipid fractions that undergo the most important changes during ripening. PL are moderately degraded during the drying process, probably due to the combined effects of the drying temperature (10°C) and the presence of starters. However, this degradation does not differ significantly between the samples that contain nitrite and and those that contain nitrate in each control. Received: 23 July 1997 / Revised version: 8 October 1997     

Effect of nitrate and nitrite curing salts on lipolysis in dry sausages produced using a rapid fermentation process

 The effect of nitrite and nitrate curing salts on lipolysis in a typical non-smoked Spanish sausage (salchichón), manufactured using a rapid dry fermentation process, was studied. From the results obtained, one could deduce that nitrite and nitrate per se do not affect the endogenous hydrolysis of the lipids during the rapid fermentation process used to produce dry sausage. Polyunsaturated fatty acids (PUFA) are liberated in greater quantities than monounsaturated (MUFA) and saturated (SFA) ones, which suggests that they are derived mainly from phospholipids. The samples that contained nitrate curing salts contained more free fatty acids (FFA) (548 mg/100 g) than those that contained nitrite curing salts (478 mg/100 g) at the end of the fermentation step, as a consequence of having undergone a preripening stage, during which significant amounts of FFA are formed. However, at the end of the ripening process, although there is a significant increase of FFA levels in all the sausages, no significant differences between samples with nitrite and those with nitrate could be found. This result could have occurred if the oxidative effects of the samples with nitrate balanced the antioxidative properties of nitrite, such that, through different processes, similar concentrations of FFA are obtained at the end of ripening. Phospholipids (PL) and free fatty acids (FFA) are the lipid fractions that undergo the most important changes during ripening. PL are moderately degraded during the drying process, probably due to the combined effects of the drying temperature (10°C) and the presence of starters. However, this degradation does not differ significantly between the samples that contain nitrite and and those that contain nitrate in each control. Received: 23 July 1997 / Revised version: 8 October 1997     

LIPOLYTIC AND OXIDATIVE CHANGES OF BARLEY LIPIDS DURING MALTING AND MASHING

Lipolytic and oxidative changes of barley lipids were studied during malting and mashing. The amount of lipid decreased by 23% during malting and changes in the composition of lipid classes were minor. On the other hand, during mashing the amount of free fatty acids (FFA) increased which indicated, that lipid hydrolysis had occurred. The same phenomenon was seen when malt flour was soaked in water at 23°C. The triglyceride (TG) and polar lipid (PL) contents were reduced and the proportion of FFA in total lipids was increased. Following similar soaking of barley flour, TG and PL were reduced but the accumulation of FFA and especially linoleic acid (LA) was slight. The results were consistent with the data on lipoxygenase activity (LOX) during malting. During steeping LOX decreased and was 15–20% of the activity of raw barley at the beginning of germination. The activity remained low during germination but rose sharply in the middle of kilning only to decrease again to a very low level at the end of kilning (5%). This in combination with the fact that the proportion of FFA remained high in the soaked malt samples suggests that the oxidation by LOX is negligible in the malt samples. However, the data suggest that mashing of barley, but not that of malt, includes the potential for the formation of highly polar lipid oxidation products.     

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。     

摄食不同来源磷脂对大鼠脂质代谢及脑内磷脂脂肪酸组成的影响

研究了摄食不同来源磷脂对大鼠脂质代谢及其脑内磷脂脂肪酸组成的影响。雄性SD大鼠按体重随机分为大豆油对照组(添加9%)、牛乳磷脂组(添加5%)、大豆磷脂组(添加5%)、蛋黄磷脂组(添加5%),喂食3周。检测了血清总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、游离脂肪酸(FFA)及肝脏TC、TG、磷脂(PL)的含量,并用气相色谱法测定了脑内磷脂脂肪酸的组成变化。结果显示:与大豆油对照组相比,3种磷脂均不同程度提高了大鼠体重、脏器指数,蛋黄磷脂效果显著;3种磷脂不同程度降低了血清TC、TG和FFA含量,牛乳磷脂降低血清FFA显著,大豆磷脂降低血清TC、TG显著,蛋黄磷脂降低FFA显著,大豆磷脂显著提升了血清HDL-C含量;3种磷脂不同程度降低了肝脏TC、TG、PL含量,牛乳磷脂与大豆磷脂降低肝脏TG、TC显著,而蛋黄磷脂降低肝脏TG显著;3种磷脂对脑内磷脂脂肪酸组成的影响各不相同,牛乳磷脂显著提高了脑内磷脂饱和脂肪酸含量,而大豆磷脂和蛋黄磷脂提高了DHA等多不饱和脂肪酸含量。研究表明,3种磷脂均有降血脂、肝脂作用,以大豆磷脂作用尤为明显,大豆磷脂和蛋黄磷脂的益智作用可能优于牛乳磷脂。     

冻融循环对熟制鲣鱼暗色肉脂质变化的影响

为探究冻融循环对熟制鲣鱼暗色肉脂质变化的影响,对熟制鲣鱼暗色肉进行冻融循环（0、2、4、6、8 次）贮藏,测定冻融过程中样品的过氧化值（peroxide value,POV）、酸价（acid value,AV）、pH值、脂质组成、脂肪酸组成等指标。结果显示,在冻融循环贮藏过程中,脂质组成发生明显变化,甘油三酯（triacylglycerol,TAG）和磷脂（polar lipid,PL）质量分数明显降低,游离脂肪酸（free fatty acid,FFA）质量分数明显升高。在冻融循环过程中暗色肉的pH值显著减小,POV和AV显著增加（P＜0.05）。脂质中总饱和脂肪酸和总多不饱和脂肪酸含量都逐渐下降,TAG和PL中脂肪酸含量明显下降,其中PL中总多不饱和脂肪酸含量下降明显,FFA中总多不饱和脂肪酸含量显著升高（P＜0.05）。主成分分析（principal component analysis,PCA）和偏最小二乘判别分析（partial least squares discriminant analysis,PLS-DA）结果表明,经过不同冻融次数的鱼肉之间存在一定的差异性,且随着冻融次数的增加脂质氧化程度不断加剧。相关性分析结果表明FFA质量分数与POV、AV呈正相关,与PL质量分数、TAG质量分数、pH值呈负相关。实验结果表明冻融循环会影响熟制鲣鱼暗色肉脂质组成,同时引起脂质的氧化分解。这为熟制鲣鱼暗色肉在运输和贮藏过程中脂质控制提供一定的理论指导。     

超高效液相色谱-静电场轨道阱高分辨质谱鉴定核桃仁的脂质构成

利用超高效液相色谱-静电场轨道阱高分辨质谱系统鉴定了核桃的脂质组.在正负离子模式下获得脂质的一级质谱和二级质谱信息后,共鉴定出4大类525种脂质分子,包括250种甘油酯、221种磷脂、18种糖脂、36种鞘脂类,含量分别占总脂质的87％、12.97％、0.02％和0.01％.甘油二酯(diacylglycerol,DG)...     

Changes in composition and functional properties of proteins and their contributions to Nham characteristics

Changes in composition and functional properties of proteins during fermentation of Nham, a Thai-fermented sausage, were studied. An alkaline-soluble fraction constituted a major protein component of Nham. The amount of each protein fraction in Nham varied, depending on the fermentation time. As fermentation proceeded, the progressive decrease in sarcoplasmic and myofibrillar protein fractions was accompanied by an increase in the alkaline-soluble fraction and non-protein constituents (P<0.05). Slow pH lowering to pH 4.6 during fermentation as a result of bacterial growth and accumulation of lactic acid affected the molecular conformation of the muscle proteins and resulted in changes in protein functional properties. The acid produced resulted in changes in solubility, water-binding capacity, textural properties, and color characteristics. Proteolysis of Nham proteins occurred during fermentation, resulting in increases in TCA-soluble peptides and free α-amino acids, which may contribute to the taste and aroma of Nham.     

The lipids of young cassava (Manihot esculenta,Crantz) leaves

Lipids were extracted quantitatively from young cassava (Manihot esculenta Crantz) leaves with a chloroform-methanol mixture. Total lipids were purified by the Folch procedure and separated into non-polar lipid, glycolipid and phospholipid fractions by column chromatography. Lipids of each fraction were further subjected to thin layer chromatography and gas-liquid chromatography. Young cassava leaves were found to have low content of lipids (3.02%) of which 22.4, 25.1 and 48.2 were non-polar lipids, glycolipids and phospholipids, respectively. Pigments (11.5%), wax and hydrocarbons (1.2%), steryl esters (2.9%), methyl esters of fatty acids (2.0%), trigly-cerides (1.5%), fatty acids (2.1%), diglycerides (1.1%) and sterols (0.1%) constituted the leaf non-polar lipids. The leaf glycolipids were made up of esterified steryl glycosides (2.1%), monogalactosyl diglycerides (12.5%), steryl glycosides (1.1%), cerebrosides (4.2%) and digalactosyl diglycerides (5.2%). The leaf phospholipids were found to include cardiolipin (3.6%), phosphatidylglycerol (21.5%), phosphatidylethanolamine (16.4%), phosphatidylserine (0.7%), phosphatidylinositol (4.0%) and other unidentified phospholipids (2.5%). Phosphatidylcholine was present only in trace quantity. Analysis of the fatty acid composition of each of the leaf lipids revealed that, with the exception of steryl esters, all leaf lipids have high content of polyunsaturated fatty acids.     

Effect of fermentation,processing and storage on lipid composition of sauerkraut

The changes in lipid composition and fatty acid distribution of sauerkraut during fermentation, canning, processing and storage were investigated organoleptically and chemically. Treatments were significant throughout the experiment. pH, lactic acid, and moisture content did not reveal any substantial changes. Total lipids, neutral lipids, and glycolipids increased, whereas phospholipids were unaltered during fermentation and processing. Quantitative changes in nonpolar and polar lipids during storage were in opposite directions, and net lipid content did not change. The changes in fatty acid composition were primarily in the distribution of palmitic, stearic, oleic, linoleic and linolenic acids during fermentation, processing and storage. Total lipids did not relate to organoleptic evaluation. However, polar lipids, specifically phospholipids, were directly related to storage stability and increased amounts of general acceptability. The formation of phospholipids may be catalysed by a reaction between tin from the cans and polar lipids at the expense of neutral lipids.     

Lipid Content and Fatty Acid Composition in Bamboo Shoots

Lipids from bamboo shoots (Phyllostachys pubescens), peeled and divided from top to base, were extracted and fractionated into three classes, and each class separated into constituent components by thin-layer chromatography (TLC). Fatty acid composition and amount of separated lipids were determined. Total lipids (TL) ranged from 800 (top) to 380 mg (base) per 100g fresh weight and the ratio of nonpolar lipids (NPL):glycolipids (GL):phospholipids (PL) was about 17:27:56. The main fatty acids of the three lipid classes were palmitic, linoleic and linolenic acids, but composition was remarkably different among these fractions. The fatty acid composition of triglycerides (TG) was similar to the original NPL. Palmitic acid was almost all located in 1-, 3-position, linoleic acid mainly located in 2-position of TG, while linolenic acid was distributed in each position. Digalactosyl diglyceride (DGDG) and monogalactosyl diglyceride (MGDG) were the main components of GL; the average of the former had about 37% linoleic and 29% linolenic acids, while the latter had about 25% linoleic and 62% linolenic acids. Bamboo shoots contained 9 PL fractions, the major being phosphatidyl choline (PC) and phosphatidyl ethanolamine (PE). PC contained about 48% linoleic, 31% palmitic and 11% linolenic acids, and PE also had the similar tendency as PC.     

Barley Neutral Lipid Changes During the Fuel Ethanol Production Process and Product Acceptability from the Dried Distillers Grains

Changes in lipids were traced from the parent barley through the fuel production process to the finished dried distillers grains (DDG). Free fatty acids (FFA) increased from 6% to 22% while the triacylglycerols (TAG) decreased from 73% to 56% during processing. Minor quantitics of ethyl esters of fatty acids, not found in the parent barley, were formed during fermentation. The fatty acid profile of the monoand diacylglycerol and TAG bands remained constant over processing, indicating that these fractions were attacked by nonspecific hydrolysis. During processing, the FFA composition changed with an increase in saturated fatty acids and a decrease in unsaturated fatty acids. Consumer taste panelists preferred commercial and ground barley supplemented granolas over granolas containing either full fat or defatted barley DDG. Trained taste panel results indicated that defatting the DDG did not result in improved product acceptability.     

Lipomobilization in periparturient dairy cows influences the composition of plasma nonesterified fatty acids and leukocyte phospholipid fatty acids

The periparturient period is characterized by sudden changes in metabolic and immune cell functions that predispose dairy cows to increased incidence of disease. Metabolic changes include alterations in the energy balance that lead to increased lipomobilization with consequent elevation of plasma nonesterified fatty acids (NEFA) concentrations. The objective of this study was to establish the influence of lipomobilization on fatty acid profiles within plasma lipid fractions and leukocyte phospholipid composition. Blood samples from 10 dairy cows were collected at 14 and 7 d before due date, at calving, and at 7, 14, and 30 d after calving. Total lipids and lipid fractions were extracted from plasma and peripheral blood mononuclear cells. The degree of lipomobilization was characterized by measurement of plasma NEFA concentrations. The fatty acid profile of plasma NEFA, plasma phospholipids, and leukocyte phospholipids differed from the composition of total lipids in plasma, where linoleic acid was the most common fatty acid. Around parturition and during early lactation, the proportion of palmitic acid significantly increased in the plasma NEFA and phospholipid fractions with a concomitant increase in the phospholipid fatty acid profile of leukocytes. In contrast, the phospholipid fraction of long-chain polyunsaturated fatty acids in leukocytes was diminished during the periparturient period, especially during the first 2 wk following parturition. This study showed that the composition of total plasma lipids does not necessarily reflect the NEFA and phospholipid fractions in periparturient dairy cows. These findings are significant because it is the plasma phospholipid fraction that contributes to fatty acid composition of membrane phospholipids. Increased availability of certain saturated fatty acids in the NEFA phospholipid fractions may contribute to altered leukocyte functions during the periparturient period.     

Characteristics of Mackerel Mince Lipid Hydrolysis

The lipid hydrolysis products in minced mackerel stored under vacuum at 2–3°C for 15 days were free fatty acids (FFA) and 1,2-diglycerides (DG); no 1,3-DG br monoglycerides were obsrved, Lysophosphati-dylcholine fLPC and lvsoohosohatidvlethanolamine (LPE) increased and then ddcreased with time: Lysiphosphatidylserie was not observed. More FFA, 1,2-DG, LPC, and LPE were detected in dark muscle than in light muscle. The initial fatty acid composition, by GC, showed no significant differences (α-0.05) among whole, light and dark muscles. When the lipid extracts were separated into three fractions (1: mostly triglycerides; 2: mostly FFA, DG, and cholesterol; and 3: mostly phospholipid), the degree of unsaturation of the lipids in fraction 2 was between those in fraction 1 and 3 and increased with time. These findings support the possibility that fish lipid hydrolysis may affect fish wholesomeness.     

Changes in wheat lipids during mixing and resting of flour-water doughs

Lipids extracted with water-saturated n-butanol from flour and flour-water doughs were examined to determine the extent of oxidations and other changes which occurred in mixing and resting dough. Extracted lipids were converted to fatty acid methyl esters (FAME) and quantified by gas-liquid chromatography (g.l.c.) using heptadecanoic acid (17 : 0) as internal standard. The original flour or dough and the corresponding solvent-extracted residues were acid hydrolysed, and the hydrolysate lipids converted to FAME for g.l.c. determination of the total lipid and residual unextracted lipid contents. The total flour or dough lipids equalled the extracted lipids + unextracted lipids, except where there were unavoidable autoxidative losses of linoleate (18 : 2) and linolenate (18 : 3). The unextracted flour lipids (13% of total lipids) were not oxidised during dough mixing. There were no changes in any of the extracted lipid classes other than free fatty acids (FFA) and monoglycerides (MG) which showed losses of 18 : 2 and 18 : 3 after aerobic dough mixing. Losses of FFA and MG are attributed to lipoxygenase activity during dough mixing and the period immediately after. The small amount of 18 : 2 in the “free” petroleum ether-extracted FFA appeared to be unaffected by lipoxygenase. Recoveries of FFA other than 18 : 2 or 18 : 3 were constant, indicating no lipolysis of glycerolipids and no general oxidation or degradation of FFA. Experiments with [U-¹⁴C]palmitic acid confirmed that there was no oxidation, degradation or re-esterification of FFA. Much of the non-polar lipids (steryl ester, triglyceride, diglyceride, FFA, MG) and almost all of the polar lipids were bound on dough mixing. Binding was non-selective with regard to fatty acid composition. Triglyceride was the only lipid class bound to a greater extent in anaerobic dough than in aerobic dough. Some selectivity of binding between lipid classes was indicated.