PHOSPHOLIPIDS AS RELATED TO TOTAL LIPID AND DNA IN LIGHT AND DARK PORTIONS OF PORCINE SEMITENDINOSUS MUSCLE

SUMMARY –Phospholipids of the light and dark tissue of porcine semitendinosus muscle were studied in relation to total lipid and DNA concentrations. The dark portion contained more moisture and less lipid than the light. Phospholipid concentration was higher in dark than light tissue whether expressed in terms of tissue weight or as percent of total lipid. No difference was found in relative concentrations of lecithin, cephalin or sphingomyelin in the two portions. DNA content was higher in the dark tissue than in the light. Expression of phospholipid content in terms of DNA resulted in a reversal of the apparent difference between the two muscle portions: the phospholipid-DNA ratio was higher for light than for dark tissue.     

Effect of Postmortem Storage on Titin and Nebulin in Pork and Poultry Light and Dark Muscles

Purified myofibrils were prepared from samples of chicken breast and thigh muscles and from light and dark portions of pork semitendinosus muscle at death and after storage at 4° and 22°C for 1, 3, and 7 days postmortem. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was used to examine the effect of postmortem storage of muscle on titin and nebulin. Results indicated that titin and nebulin were more rapidly degraded in light than in dark chicken muscle. In contrast, titin and nebulin were more rapidly degraded in dark than in light pork muscle.     

Profile of fiber types in muscles from wild pigs native to the United States

Histochemical and histological parameters of the longissimus (LD) and semitendinosus (dark and light portions) muscles from wild pigs native to Florida, USA, were investigated. All three fiber types were present in both muscles at varying proportions with typical (red fibers grouped in clumps and surrounded by white fibers) fiber arrangements for domestic porcine muscles (Cassens, 1971), contrary to the findings by Rahelic & Puac (1981), who examined the LD muscle of wild pigs native to Yugoslavia. These authors foud only βR fibers present in the LD muscle. In five of the six pigs in the present study, extremely and abnormally large fibers (giant fibers), possessing βR fiber characteristics, were observed. These giant fibers were found in both the LD and the semitendinosus (dark and light portions) and were not restricted to the periphery of the fasiculi. The presence of these giant fibers suggests some type of muscle myopathy syndrome in these pigs.     

Distribution of the Lipid Classes and Eicosapentaenoic (20:5) and Docosahexaenoic (22:6) Acids in Different Sites in Blue Mackerel (Scomber australasicus) Fillets

The distribution of lipid in various sites of the edible fillets of the blue mackerel (Scomber australasicus) was determined. Specific details of the lipid composition of the dark and white muscles were provided by column and thin layer chromatography. Dark muscle contained 20% lipid whereas white muscle had only 4% lipid. However, white muscle lipid was relatively much higher in phospholipids; 19% vs 10% in dark muscle lipid. The major phospholipids were phosphatidylcholine, phosphatidyl ethanolamine, and sphingomyelin. These were distributed in similar proportions in both muscles, although the white muscle phospholipids included more polyunsaturated [cicosapentaenoic (EPA) and docosahexaenoic (DHA)] acids than those of the dark muscle.     

Species and muscle differences in L-carnitine levels in skeletal muscles based on a new simple assay

We have adapted the enzymatic method [Biochemical and Biophysical Research Communications 176 (3) (1991) 1617] for the safe and rapid assay of L-carnitine (L-CA) in skeletal muscle using a microplate reader. The concentration of L-CA in fresh semitendinosus muscle from broiler chicken, pig, beef cattle, deer, horse and goat muscle were 0.69, 1.09, 1.86-3.57, 4.57, 4.95 and 11.36 μmol/g wet weight, respectively. The animals which had higher concentration of L-CA, also had the highest amounts of myoglobin as an index to the redness of the muscle. Furthermore, we investigated this relationship between white muscle, M. pectoralis profundus, and red muscle, M. soleus, in laying hens. The L-CA and myoglobin concentration in red muscle were significantly higher than those in white muscle (p<0.01). These findings suggest that L-CA concentration in muscle is related to oxygen metabolism and to myofiber types.     

Physicochemical characterization of muscle proteins from different regions of mackerel (Rastrelliger kanagurta)

Physicochemical characteristics of proteins extracted from muscles excised from four distinct regions of mackerel were examined. Three regions were identified based on their fin position; namely anterior muscle, median muscle, posterior muscle and red muscles from beneath the lateral line. The biochemical characteristics like reactive sulphydryl groups, surface hydrophobicity, Ca²⁺ ATPase activity, turbidity, proximate composition and the functional characteristics such as viscosity, emulsion activity index (EAI) and emulsion stability (ES) were studied in the samples, from different regions. Sarcoplasmic protein (SPP) solubility was found to be higher in red muscles compared to that of white muscles, whereas myofibrillar protein (MFP) solubility was higher in white muscles particularly in the posterior portion. The MFP from posterior white muscles showed better viscosity, surface hydrophobicity and Ca²⁺ ATPase activity, which in turn contributed to the higher EAI and ES of this muscle portion. Variations in composition, electrophoretic pattern of proteins and selected functional properties (EAI) were noticed between red and white muscles, which may be of significance from the utilization point of the fish.     

Intramuscular fatty acid profile of longissimus dorsi and semitendinosus muscle from Kundi steers fed on pasture with cottonseed cake supplement

The present study was accomplished to evaluate the intramuscular fatty acid (FA) composition of different muscles taken from Kundi steers (n = 15), which were approximately 24 months old, fed on a cottonseed cake supplement, and were made to graze on alfalfa pasture for 95 days prior to slaughter. The samples were taken from longissimus dorsi region (loin and ribeye portion) and distal region of semitendinosus muscle for intramuscular FA analysis. Saturated FA, comprising 49.48–52.09% of total FA composition, in all the muscles were studied. Ribeye portion of longissimus dorsi muscle contain relatively higher (P > 0.05) amount of trans FA (3.37%) as compared with loin portion of longissimus dorsi muscle (3.1%) and distal region of semitendinosus muscle (2.84%). The sum of monounsaturated FA in all the muscles studied was estimated in the range of 32.21–34.64%, while polyunsaturated FA contribute 11.39–12.39% of total FA. The mean conjugated linoleic acid was found to be 0.28, 0.35 and 0.41 in ribeye and loin portion of longissimus dorsi muscle and distal region of semitendinosus muscle, respectively.     

Method of isolation, rate of postmortem metabolism, and myosin heavy chain isoform composition influence ATPase activity of isolated porcine myofibrils

The objective of this study was to determine the influence of myofibril isolation procedures and myosin heavy chain (MyHC) isoform composition on myofibrillar ATPase activity as related to postmortem muscle metabolism. Myofibrils from the red (RST) and white (WST) portions of semitendinosus muscles were isolated using two different methods (A and B) at 3 min and 24 h postmortem in control (NS) and electrically stimulated (ES) pork carcasses. Comparison of the relative MyHC isoform profiles between the two different myofibril isolation methods and myosin extracts from the RST and WST at 3 min showed that method B myofibrils were more similar to the myosin extract than method A. Myofibrillar ATPase activity remained constant or increased (P<0.01) from 3 min to 24 h postmortem in NS carcasses and decreased (P<0.0001) in ES carcasses. From the RST, method A myofibrils had higher (P<0.0001) ATPase activity compared to method B across sampling time and carcass treatment. In the WST, method A myofibrils had lower (P<0.01) activity at 3 min, were not different at 24 h in NS carcasses, but had higher (P<0.05) activity at 24 h in ES carcasses versus method B myofibrils. Compared to method B, isolation method A biased the isoform profile of myofibril samples more towards faster MyHC (2A and 2X) in the RST and towards MyHC 2X in the WST. Results suggest that the ATPase activity and MyHC isoform profile of isolated myofibril samples are influenced by method of myofibril isolation, postmortem sampling time, and the rate of postmortem metabolism. Thus, differences in MyHC isoform profile and method of myofibril isolation must be taken into account to determine accurately the relationship between myofibrillar ATPase activity and rate of postmortem metabolism.     

Comparative studies of quality changes in white and dark muscles from common carp (Cyprinus carpio) during refrigerated (4 °C) storage

Differences between white and dark muscles from common carp (Cyprinus carpio) in sensory assessment, total viable counts (TVC), total volatile basic nitrogen (TVB‐N), pH, electrical conductivity (EC), biogenic amines (BAs), nucleotide degradation products and colours were investigated under air and vacuum conditions during refrigerated (4 °C) storage. Compared with white muscle, dark muscle had a higher lipid content, but lower crude protein and moisture content. TVC, TVB‐N, pH, and L* value were higher in white muscle, while K value and a* value were higher in dark muscle. Under both conditions, white and dark muscles had significant (P < 0.05) differences in tyramine and cadaverine content. Although dark muscle was significantly (P < 0.05) lower in ATP content, it had higher rate of IMP degradation and K value increase. Taking sensory and microbial indexes into consideration, dark muscle appeared to have a longer shelf life than white muscle under both conditions.     

Changes in Free Amino Acids and Creatine Contents in Yellowtail (Seriola quinqueradiata) Muscle during Ice Storage

Free amino acids (FAA) and creatine contents of white and dark muscles of yellowtail (Seriola quinqueradiata) were measured and compared during ice storage. White muscle contained a large quantity of free histidine (1,160 mg/100g), while an equally large amount of taurine (1,150 mg/100g) was present in the dark muscle. Little change in the levels of most FAA occurred in the white muscle during ice storage for over 40 days but in the dark muscle the levels of almost all FAA except taurine increased significantly over a period of 33 days. Creatine was present in higher concentration in the white than in the dark muscle (510 vs 170 mg/100g), while its level did not change in either muscle during the entire storage period.     

Color Stability, Lipid Stability, and Nutrient Composition of Red and White Veal

Surface spectra of the two veal types revealed that red veal was more discolored than white veal by day 6 of 4° C storage (P<0.05). Measurements of MetMb accumulation in minced muscle revealed a greater concentration of oxidized pigment for red veal on days 2 and 4 of 4° C storage (P<0.05). Data support a tendency of red veal to undergo more rapid lipid oxidation than white veal during storage. There were no differences between the two veal types for pH, proximate analysis or fatty acid composition (P < 0.05). However, red veal contained higher levels of iron and zinc, and lower levels of cholesterol than white veal (P<0.05). The results indicate that while red veal has a more limited shelf-life than white veal, it also has potential nutritional advantages.     

Lipid Hydrolysis and Oxidation Related to Astaxanthin Content in Light and Dark Muscle of Frozen Stored Rainbow Trout (Oncorbynchus mykiss)

Astaxanthin decreased significantly during frozen storage in both light and dark muscle of farmed rainbow trout (Oncorhynchus mykiss). Astaxanthin sunolementation did not affect lipid hydrolysis and oxidation during frozen storage of fish muscle. Deposition of astaxanthin was higher in dark muscle than in light muscle. Astaxanthin decreased in both supplemented and nonsupplemented fish. The sum of trans-astaxanthin and its cis-isomers decreased during frozen storage, indicating mechanisms other than trans-cis isomerization were causes. α-Tocopherol decreased to the same extent in both light and dark muscle for both diets.     

宰后成熟对牛胴体不同部位显微结构影响

将不同部位肉样真空包装后于4℃条件下成熟72h ,采用石蜡切片苏木精-伊红(HE)染色法、原子力显微镜扫描肌原纤维、环境扫描电镜扫描肌纤维膜、免疫组织化学法及测定剪切力,研究牛胴体不同部位剪切力、宰后成熟过程中肌纤维和肌原纤维裂解程度、肌纤维膜变化及μ-calpain肌纤维定位。结果表明：剪切力：半腱肌＞腹直肌＞背最长肌;牛肉后熟过程中,背最长肌肌纤维、肌原纤维裂解程度最大,腹直肌次之,半腱肌变化较小;肌纤维膜变化不大;μ-calpain主要存在于肌纤维膜和肌浆中,红肌纤维(慢肌)μ-calpain含量高,白肌纤维(快肌)μ-calpain含量低。μ-calpain在牛肉后熟过程中对牛肉嫩化具有重要作用,红肌纤维μ-calpain含量高,白肌纤维μ-calpain含量低,因此,胴体不同部位红肌纤维和白肌纤维的比例是导致其后熟嫩度和显微结构差异较大的一个重要因素。     

Myosin heavy chain isoforms influence myofibrillar ATPase activity under simulated postmortem pH, calcium, and temperature conditions

The pH and Ca(2+) sensitivity of myofibrillar ATPase activity plays an integral role in regulating postmortem muscle ATP utilization and likely paces postmortem glycolysis. The objective of this study was to determine the influence of pH and Ca(2+) concentration on the ATPase activity of myofibrils from red semitendinosus (RST) and white semitendinosus (WST) porcine muscles. Myofibrillar ATPase was measured at 39 °C over a pH range 5-7.5 and a [Ca(2+)] range pCa 4-9 (10(-4)-10(-9)M). At maximum Ca(2+)-dependent activation (pCa 4), RST myofibrils had lower (p<0.0001) ATPase activity than WST myofibrils. This maximum activity of myofibrils from both muscle regions was not influenced from pH 7.5 to 6.5, declined between pH 6.5 and 5.75 (Hill coefficient, n(H)=2.7-3.4; pH at half maximum activity, pH(50)=5.97) and was near zero at pH 5.5. At pH 7, pCa-activity relationships showed that RST required less Ca(2+) for half-maximum activation (higher pCa(50); 6.50) than WST myofibrils (pCa(50)=6.35) but had no difference in n(H). At pH 7, both RST and WST myofibrils had maximum Ca(2+)-dependent, actin-activated ATPase activity at pCa ?6 and Ca(2+)-independent myosin ATPase activity at pCa ?6.75. pCa-activity relationships at different pH levels indicated that pCa(50) decreased with pH from pH 6.5 to 6.125 in both RST and WST myofibrils. At pH <5.75, [Ca(2+)] did not influence ATPase activity in RST or WST myofibrils. These data show that myofibrils with predominantly fast MyHC (WST) have a higher actin-activated myosin ATPase activity than myofibrils with primarily slow MyHC isoforms (RST) at Ca(2+) concentrations and pH values characteristic of postmortem muscle.     

Cholesterol concentration and fatty acid profile of red deer (Cervus elaphus) meat

The effects of gender and age on intramuscular fat (IMF) levels, cholesterol concentration, and fatty acid composition were investigated in the semitendinosus (ST) and triceps brachii (TB) muscles of feral red deer (Cervus elaphus). Six stags of >2years of age, four hinds of 1year, and six calves of 6months were shot in Slovenia. Generally, all parameters measured were influenced by interaction of muscle and treatment group (hinds, stags and calves) at the 5% level or less. In ST muscle, the IMF levels were highest for hinds. In the TB muscle, cholesterol was lower for stags than for hinds and calves. The saturated fatty acids were the highest for stags and the mono-unsaturated fatty acids for hinds. The polyunsaturated fatty acids (PUFAs) were the highest for calves and lowest for hinds. The n-3 PUFAs were the lowest for hinds. In both muscles, the calves had higher n-6 PUFAs than stags and hinds. Only the ST muscle of the hinds contained >1% (1.44%) of the conjugated linoleic acid isomer 18:2cis-9,trans-11, while in the TB of hinds and calves this fatty acid was higher than with stags. We conclude that gender and age of feral red deer influence the IMF content, the cholesterol concentration, and the fatty acid composition of the meat.     

不同光质萎凋对贡眉白茶滋味品质的影响

为筛选改善贡眉白茶滋味的最优萎凋光质,采用LED精量调制光源,通过感官审评法、超高效液相色谱串联三重四级杆质谱、高效液相色谱等方法,研究无光(对照)、日光、蓝光、黄光和红光萎凋,对贡眉白茶的感官品质、主要生化成分、部分代谢物的影响。结果表明,4个光照组感官审评的滋味、香气及总得分,均比无光组高,且红光滋味得分最高。相比无光和其他光质组,红光组的可溶性糖、水浸出物、咖啡碱、没食子儿茶素没食子酸酯、茶氨酸、苏氨酸、谷氨酸、谷氨酰氨、甘氨酸、丙氨酸、γ-氨基丁酸及总氨基酸的含量最高,有益于“醇厚鲜甜”的滋味特征形成。相比无光组,4个光照组显著降低部分黄酮(醇)苷的含量(P<0.05),红光组的茶黄素和茶黄素-3-没食子酸酯的含量显著降低(P<0.05),而黄、蓝、白光组的山奈酚含量显著升高(P<0.05)。综合认为,红光萎凋对白茶滋味提高最有益。     

Apparent shear viscosity of native egg white

Temperature and shear dependency of the apparent viscosity of the thick and thin portions of egg white from fresh hen eggs, in their native state was investigated. The viscosity of the egg white was determined in the temperature range of 5–30°C and the shear rate range 34–600 sec^-1. The viscosity of both the thick and thin portions of the egg white decreased with increase in temperature. The thin portion showed no decrease in viscosity with shearing time at constant shear rates while the viscosity of the thick portion decreased within the first 6 min of shearing and then remained constant. The rate of decrease in viscosity with shearing time was more at higher temperatures. At 20°C and a shear rate of 34.2 sec^-1, the equilibrium-apparent viscosity of the thick portion was 160 cp, approximately forty times greater than that of the thin portion (4cp). This difference in viscometric properties may be due to the presence, in the thick portion, of high molecular weight complexes which are disrupted under shearing.     

Concentrations in beef and lamb of taurine, carnosine, coenzyme Q(10), and creatine

Levels of taurine, carnosine, coenzyme Q(10), and creatine were measured in beef liver and several muscles of beef and lamb and in cooked and uncooked meat. The amino acid taurine has numerous biological functions, the dipeptide carnosine is a buffer as well as an antioxidant, coenzyme Q(10) is also an antioxidant present within mitochondria, and creatine along with creatine phosphate is involved with energy metabolism in muscle. Large differences were shown for all compounds between beef cheek muscle (predominantly red fibres) and beef semitendinosus muscle (mainly white fibres), with cheek muscle containing 9.9 times as much taurine, and 3.2 times as much coenzyme Q(10), but only 65% as much creatine and 9% as much carnosine. Levels in lamb relative to beef semitendinosus muscles were higher for taurine but slightly lower for carnosine, coenzyme Q(10) and creatine. Values for all the compounds varied significantly between eight lamb muscles, possibly due in part to differences in the proportion of muscle fibre types. Slow cooking (90 min at 70?°C) of lamb longissimus and semimembranosus muscles led to significant reductions in the content of taurine, carnosine, and creatine (P<0.001), but a slight increase in coenzyme Q(10). There was also a four-fold increase in creatinine, presumably due to its formation from creatine. It is concluded that biologically, and possibly nutritionally, significant levels of taurine, carnosine, coenzyme Q(10), and creatine are present in beef and lamb, but that these levels vary between muscles, between animals, and with cooking.     

Fatty acid composition of intramuscular lipids in various muscles of Holstein-Friesian bulls slaughtered at different ages

Holstein-Friesian bulls were slaughtered at 7, 14 and 19 months of age. Samples were collected from the psoas major, longissimus and semitendinosus muscles. The total lipids (TL) of the samples were extracted and the fatty acid compositions were analysed by gas chromatography. Both the slaughtering age and the type of muscles had significant effects on the intramuscular TL contents and fatty acid compositions. The longissimus muscle had higher intramuscular TL both at 14 and 19 months than at 7 months of age. As the bulls became older the proportion of saturated fatty acids (SFA) and monounsaturated fatty acids (MUFA) increased in the TL of each muscle tested, whereas that of polyunsaturated fatty acids (PUFA) decreased. Among the muscle types, the semitendinosus had the lowest, intramuscular TL at each slaughtering age and the psoas major the highest. Except for SFA at 7 months of age, the semitendinosus showed lower levels of SFA and MUFA and higher proportions of PUFA than the other two muscles.