Paris ham processing: Technological yield as affected by residual glycogen content of muscle

The aim of the present experiment was to study the relationships between pH, protein and residual glycogen content of pig muscle on the one hand, and technological yield (TY) of Paris ham processing on the other (Paris ham is a type of cured cooked ham). Fifty-two pigs were slaughtered at 100 kg liveweight in a commercial abattoir, in four slaughter series. Ultimate pH, protein and glycogen were determined around 24h post mortem. Two days after slaughter, the right hams were processed to Paris ham. Residual glycogen levels varied from 0 to 78 μmol/g of fresh tissue. All correlations between TY and the other traits under study were significant at the P < 0·05 level. Correlation between glycogen and TY was by far the highest one (r = 0t-0·60, P < 0·01). Protein content and both pH values gave similar but lower correlations with TY (r around 0·4, P < 0·01). It is concluded that the results of the present study agree with the hypothesis that the residual glycogen content of muscle has a direct effect on the technological yield of cooked ham processing.     

Postmortem regulation of glycolysis by 6-phosphofructokinase in bovine M. Sternocephalicus pars mandibularis

This experiment addressed the hypothesis that 6-phosphofructokinase (6-PFK) regulates glycolysis in postmortem in M. sternocephalicus pars mandibularis. In two separate experiments, muscle samples were excised from randomly-selected steers that would typically be found on a commercial slaughter floor. In the first experiment, two samples were obtained from each of 6 steers immediately post-exsanguination; one sample was immersed immediately in liquid nitrogen and the other was stored at 4 °C for 4 d, to compare 6-PFK enzyme activity and glycolytic intermediate concentrations between fresh and d 4 postmortem samples. The greatest activity of 6-PFK was measured in fresh muscle extracts at pH 7.4, whereas little activity was detectable at pH 7.0. 6-PFK activity measured at pH 7.4 in d 4 samples also was barely detectable. Hill coefficient values for 6-PFK in fresh samples measured at pH 7.4 or 7.0, and d 4 samples measured at pH 7.4 were 2.9, 0.8, and 0.7, respectively, indicating loss of cooperativity with both lowered pH during assay and with time postmortem. Glycogen concentrations decreased 45% from d 0 to d 4, to 39.6 μmol glycogen/g muscle. Muscle concentrations of free glucose increased (P < 0.001) from 0.84 μmol/g at d 0 to 6.54 μmol/g at d 4. Fructose-6-phosphate and glucose-6-phosphate increased (P < 0.001) from d 0 to d 4 (2.8-fold and 4.7-fold, respectively). Lactate began accumulating immediately (3.33 μmol/g) and was elevated to 45.9 μmol/g by d 4. In the second experiment, conversion of [U-¹⁴C]glucose to lactate, glycogen, and CO₂ was measured in vitro at pH 7.4 and 7.0 in fresh M. sternocephalicus pars mandibularis strips from four steers. Total [U-¹⁴C]glucose was less in muscle strips incubated at pH 7.0 than in those incubated at pH 7.4 (55.5 vs. 123 nmol glucose utilized per 100 mg muscle per h; P = 0.04), due primarily to a reduction in glucose conversion to lactate. The conversion of glucose to glycogen or CO₂ in vitro was unaffected by media pH. These results suggest that the postmortem decline in pH in M. sternocephalicus pars mandibularis ultimately inactivates 6-PFK; this occurs prior to the depletion of glycogen reserves.     

Muscle glycogen depletion pattern in halothane-gene-free pigs at slaughter and its relation to meat quality

Muscle fibre type composition and glycogen depletion pattern at slaughter as related to meat quality, were studied in M. longissimus dorsi of halothane-gene-free Swedish Yorkshire pigs fed a high (n=19; 10 entire males and 9 gilts) or a low (n=18; 10 entire males and 8 gilts) protein diet. The muscle consisted of, on average, 8% type I, 9% type IIA and 83% type IIB fibres. Muscle fibre areas were significantly smaller in entire male pigs than in gilts irrespective of fibre type. There were no marked differences in muscle characteristics between pigs fed the low and high protein diets. Low glycogen concentrations were found in most type I and type IIA muscle fibres, while a greater variation in glycogen content was evident in type IIB fibres. The pigs were divided into two groups according to the proportion of glycogen depleted IIB fibres (more or less than 30% depleted IIB fibres). In the group where 30% or more of the type IIB fibres were glycogen depleted, a tendency toward DFD meat (dry, firm, dark) was seen, as the meat had higher ultimate pH (5·62 vs 5·52; p=0·02), lower drip loss (2·7% vs 4·4%; p=0·007) and lower reflectance value (darker meat; 16·5 vs 20·6 EEL units; p=0·0005), compared with the group with less than 30% depleted IIB fibres. No difference in total glycogen content was found between these two groups. This indicates that the distribution of glycogen in different fibre types seems to be of importance for the ultimate meat quality.     

Plasma and muscle cortisol measurements as indicators of meat quality and stress in pigs

Post-slaughter blood samples and muscle samples were collected from pigs slaughtered at the completion of a live-animal performance trial. There were two lines of pigs in which the halothane allele (n) was segregating. The lines were a lean line selected for rapid lean growth and an unselected fat line. There were homozygous normal (NN), homozygous halothane positive (nn) and heterozygous (Nn) genotypes in both lnes. Cortisol was measured in the plasma of the blood samples and in muscle juice obtained by high-speed centrifugation. Meat quality was assessed using pH, colour, fibre-optic probe, drip loss and cure yield measurements. Plasma cortisol concentrations in the fat line were significantly (P < 0·05) greater than thosein the lean line but concentrations did not differ significantly for the three halothane genotypes. Carcasses classified as dark, firm and dry (DFD) had significantly (P < 0·05) greater muscle cortisol concentrations than those classified as normal. Plasma and muscle cortisol concentrations of carcases classified as pale, soft and exudative (PSE) did not differ significantly from those classified as normal. Correlations between muscle cortisol and meat quality attributes were generally highly significant (r = 0·31 to r = 0·51, P < 0·001) There was a highly significant correlation (r = 0·73, P < 0·0001) between plasma and muscle cortisol concentrations.     

Effects of early post-mortem ageing on intramuscular collagen stability, yield and composition

Post-mortem changes in the composition and physical stability of bovine intramuscular collagen were evaluated during a 24 h ageing period. The yield of intramuscular connective tissue (IMCT) isolated from the infraspinatus muscle samples and the carbohydrate content of that material did not change significantly (P > 0·05) during the ageing period. The collagen content and total protein content of the isolated IMCT increased (P < 0·05) through 8 h post-mortem. Moisture content of the isolated material decreased numerically but not significantly (P > 0·05). Collagen thermal shrinkage temperature (T(s)) decreased (P < 0·01) and collagen solubility increased (P < 0·05) during the ageing period with most of the changes occurring in the first 8 h.     

Effect of epinephrine administration on glycogen metabolism in red and white muscle of anaesthetized pigs (Sus scrofa domesticus)

The glycogenolytic effect of exogenous epinephrine was studied in white (Longissimus) and red (Trapezius) muscle of anaesthetized pig. In addition, we assessed the metabolic action of epinephrine during the 3 h following the cessation of perfusion. Twelve purebred Large White pigs, averaging 80 kg live-weight, were used. The animals were anaesthetized and perfused (0–15 min) with 5 μg kg^?1 min^?1 epinephrine or saline (control animals). Blood samples were taken to determine plasma levels of glucose, lactate and non-esterified fatty acids (NEFA). Muscle samples were taken to determine the concentrations of glycogen and related metabolites, and the activity ratio of the enzyme glycogen phosphorylase. Control animals showed stable levels of plasma and muscle metabolites during the 3 h anaesthesia. However, the resting level of the activity ratio of phosphorylase was high (80%). Epinephrine treatment induced significant increases in plasma metabolites and an overall significant glycogen depletion. The extent of epinephrine-induced glycogenolysis was greater in the red Trapezius than in the white Longissimus muscle. This was associated with a greater rise in the muscle lactate content and in the activity ratio of phosphorylase in the Trapezius muscle during epinephrine administration. In both muscles, no significant glycogen depletion was observed during 3 h following the cessation of epinephrine administration. This occurred despite the fact that the activity ratio of phosphorylase remained high in the Longissimus muscle until the end of the experiment.     

The relative effect of dietary energy density on repleted and resting muscle glycogen concentrations

The aim of this study was to assess the effect of dietary energy density on the glycogen concentration of bovine gluteus medius (GM) and longissimus thoracis et lumborum (LTL) muscles in castrated and intact males. Cattle received diet C (90% whole corn and supplement: 10% alfalfa haylage) or diet AH (100% alfalfa haylage) in three experiments involving a 2×2 factorial cross-over design. Cattle fed an AH diet for 70 days prior to the first experiment had high glycogen concentrations in the GM (129±9.9 mmol/kg) and LTL (108±7.6 mmol/kg) at the first biopsy session. These concentrations are similar to GM (133±6.2 mmol/kg) and LTL (105±5.8 mmol/kg) glycogen concentrations when these cattle subsequently received diet C for 30 or 37 days. Diet C increased muscle glycogen concentration, but the consistency of the increase in glycogen was dependent on the initial concentration. When the initial glycogen concentration was depleted to 50 μmol/g with one subcutaneous injection of adrenaline, repleted glycogen concentration was higher for diet C than AH (P<0.01) in all comparisons involving GM and LTL muscles of both steers and bulls. For resting muscle glycogen, the GM of bulls was more sensitive to the effect of diet C than the bull LTL or either muscle in steers. Diet was not a major determinant of resting muscle glycogen concentration. The ultimate pHs of GM, LTL and semimembranosus (SM) were not affected by diet and residual glycogen was lower in LTL of bulls fed either diet than for LTL of steers fed AH. Diet and male status did not affect residual glycogen in GM or SM.     

The effect of oestrus behaviour on muscle glycogen concentration and dark-cutting in beef heifers

Preliminary observations at an abattoir showed an association between oestrus behaviour and dark-cutting in beef. Two follow-up experiments examined the relationship between oestrus behaviour and muscle glycogen content, carcass bruising and meat ultimate pH. In the first experiment heifers in oestrus were compared with controls in mid-cycle. Oestrus was associated with a loss of glycogen in M. longissimus dorsi. Also plasma creatine kinase activity increased, reflecting bruising or strenuous muscle activity. In the second experiment heifers were slaughtered during oestrus. On the basis of pre-slaughter behaviour they were assigned to active or inactive groups, which subsequently yielded 39% and zero dark-cutting carcasses, respectively. Loss of muscle glycogen was accounted for by the number of times an animal mounted (r = -0·85). Likewise, variation in meat ultimate pH was associated with mounting activity (P < 0·001). Carcass bruising was higher in the active group (P < 0·0.001) and the main cause of bruising was being mounted (r = 0·74). It was concluded that single penning of oestrus heifers to eliminate mounting activity would reduce the incidence of dark-cutting.     

Effect of sodium chloride concentration on pH, water-holding capacity and extractable protein of prerigor and postrigor ground beef

Fifteen beef cattle of similar age and management history were randomly allotted by slaughter days into three groups. Paired sternomandibularis were removed immediately following bleeding and trimmed of visible fat and connective tissue. They were randomly labelled as prerigor and postrigor and assigned to a 0, 0·5, 1·0, 2·0 or 4·0% NcCl treatment. Water-holding capacity (WHC), pH, the ratio of absorbance at 250 nm over the absorbance at 260 nm (R-values), and 1·0m NaCl extractable protein (EP) were monitored over treatment times. The 0 h samples were defined as when the NaCl was incorporated with the muscle. R-values verified that 0 h samples were in the prerigor or postrigor state. Ultimate pH remained higher (P < 0·05) in prerigor homogenates with increasing NaCl concentration. EP and WHC were higher (P < 0·05) in prerigor than in postrigor homogenates with 2 and 4% NaCl at all time periods. Prerigor homogenates containing 0·5 and 1·0% NaCl had higher (P < 0·05) WHC at 12, 24, 24, 48 and 96h than similarly treated postrigor homogenates and as high or higher WHC than any postrigor treatment. Results of this study indicate an advantage to using low NaCl concentrations in prerigor salted beef.     

The influence of pre-slaughter oral loading of acid or base on post-mortem changes in Longissimus Dorsi muscle of pork

Twenty-four pigs were assigned to one of four ad libitum water treatments: control, sodium bicarbonate (12·6 g/litre), low ammonium chloride (4 g/litre) or high ammonium chloride (8 g/litre) for 5 days, to study the influence of an oral acid or base load on post-mortem changes in longissimus dorsi muscle and ultimate pork quality. Physiological changes before slaughter were monitored by measuring blood pH, pCO(2) and HCO(3)(-). The influence of dietary treatments on post-mortem changes and ultimate meat quality was determined by measuring glycolytic enzymes and intermediates, and muscle pH, color and water-holding capacity (WHC). As expected, sodium bicarbonate generated a metabolic alkalosis, whereas ammonium chloride resulted in a metabolic acidosis. Pre-slaughter acid-base status was positively correlated with muscle WHC (P < 0·05). However, no significant dietary treatment effect was observed in muscle quality traits such as color (a, b, L) and WHC. Muscle pH(45) was significantly (P < 0·05) higher in bicarbonate than control and high ammonium chloride treatments. The activity of Ca(2+)-dependent protein kinase was significantly (P < 0·05) higher at 45 min post-mortem but that of pyruvate kinase was significantly lower at 2 and 4 h post mortem in bicarbonate-treated pigs. At 45 min post mortem, the activity of fructose-1,6-diphosphatase in the control pigs was significantly higher (P < 0·05) than on other treatments. The concentration of glycogen was significantly (P < 0·05) higher in bicarbonate and high ammonium chloride pigs; bicarbonate-treated pigs also has significantly higher adenosine-5'-triphosphate (ATP) and pH values than other treatment groups (P < 0·05) at early post-mortem. It was concluded that pre-slaughter oral loading of acid or base could induce changes in muscle metabolism and post-mortem muscle pH. Further research is required to confirm that altering diet acidogenicity or alkalinogenicity may be a means of enhancing ultimate pork quality.     

Optimisation of calcium-dependent protease and cathepsin D assays in ostrich muscle and the effect of chemical and physical dry-curing parameters

The best conditions for the assay of cathepsin D and Ca²⁺-dependent pro tease (CDP) activity in ostrich muscle was established in order to have a simple, rapid and reliable method for its determination. Measurements of A_280nm of TCA-soluble peptides and amino acid digests of casein and haemoglobin were used for measuring proteolytic activity in muscle extracts. The best conditions for the reliable determination of cathepsin D activity were found to be the incubation of an enzyme extract for 1 hr at 55 °C in a reaction mixture containing 0.9% (w/v) haemoglobin in 50 mM sodium formate buffer, pH 3.7. Characterization of the assay system for CDPs, obtained after phenyl-Sepharose chromatography, indicated that proteolytic degradation of casein by CDPs was linear with time up to 30 min at 30 °C and up to 0.1 units of activity. The effect of NaCl, KCl, nitrate, ascorbic acid, phosphate, glucose and sucrose on ostrich muscle CDP and cathepsin D activities has been studied. Salt (NaCl and KCl) acts as a strong inhibitor of proteolytic activity. Sodium and potassium nitrates (in the range 0–1000 mg l⁻¹) affected activity to varying degrees. CDP activity was enhanced by sodium nitrate concentrations below 700 mg l⁻¹ and unchanged by potassium nitrate. Cathepsin D activity was inhibited to some extent by sodium nitrate above 200 mg l⁻¹ and completely by potassium nitrate. Results showed that phosphate is an inhibitor of both activities. High concentrations of ascorbic acid (above 6 g l⁻¹) inhibited cathepsin D activity. Glucose (up to 2g l⁻¹) activated cathepsin D activity and inhibited CDP activity (up to 1 g l⁻¹). Sucrose activated enzyme activities at very low concentrations (1 × 10⁻³ M) and inhibited activities above 1 × 10⁻³ M.     

Influence of repeated restraint and isolation stress and electrolyte administration on carcass quality and muscle electrolyte content of sheep

Crossbred lambs were assigned, within weight blocks, to one of four treatments applied in a 2 × 2 factorial design (n = 6 per treatment). Treatment main effects included no stress (NS) or three consecutive days of restraint and isolation stress (RIS) and treatment with either water (W) or electrolytes (E). The experimental design resulted in four treatments, namely NS-lambs given W, NS-lambs given E, RIS-lambs given W, and RIS-lambs given E. Stress treatment consisted of moving each lamb from its home stanchion to a separate location and isolation from visual and tactile contact with other lambs for 6 hours daily for 3 days before slaughter. All lambs received a 320 ml oral drench of either W or E on each day after the stress treatment. Stress treatment reduced (P < 0·05) semitendinosus (ST) muscle glycogen by 4·8-fold. At 24 h post mortem, muscle pH for semimembranosus (SM), biceps femoris (BF) and infraspinatus (IF) was higher (P < 0·05) in RIS-lambs that in NS-lambs. Hunter L(?)a(?)b(?) values, measured on muscle cross-section, revealed a lighter (P < 0·05) BF; more (P < 0·05) red BF, ST, and longissimus dorsi (LD); and more (P < 0·05) yellow ST, SM, BF, and LD for NS-than for RIS-lambs. Muscle from RIS-lambs contained less (P < 0·05) potassium than that from NS-lambs. Restraint and isolation stress of lambs resulted in a reduction in muscle glycogen, but only slight increases in ultimate pH and minimal influences on muscle color. Administration of electrolytes had no effect on lamb carcass quality.     

The significance of the activity of glycogen debranching enzyme in glycolysis in porcine and bovine muscles

The purpose of the study was to examine the activity of glycogen debranching enzyme, GDE, in porcine and bovine muscles differing in rate of contraction and oxidative capacity. The activity of GDE, the activity of phosphorylase, total glucose content, lactate content and pH were measured from meat samples taken 35min post-mortem and ultimate pH 24 or 48h post-mortem. Both GDE and phosphorylase are needed for the complete degradation of glycogen. In porcine muscles the activities of these glycogen degrading enzymes were higher than in bovine muscles. The activities were increasing with the increasing fast twitch and glycolytic character of a muscle of a given species. However, the increase in the activity of phosphorylase was greater than the increase in the activity of GDE. It was concluded that the GDE may restrict the rate of glycolysis in fast twitch muscles.     

Effect of microbial transglutaminase on gel properties and film characteristics of gelatin from lizardfish (Saurida spp.) scales

The addition of microbial transglutaminase (MTGase) generally increased the gel strength of lizardfish (Saurida spp.) scale gelatin gels (P≤0.05) with an increase in gel strength with the addition of MTGase up to 0.5% (w/v). The texture profile analysis compression tests of lizardfish scale gelatin gel with and without MTGase were studied to determine their effects on gel characteristics. MTGase added to the gels decreased the band intensity of the β- and α-components with increasing concentrations of enzyme. Gel microstructures with various concentration of MTGase showed denser strands in the gels with enzyme compared with the looser stands in non-enzyme-treated gel samples. Films cast from lizardfish scale gelatin with and without 0.5% MTGase and bovine gelatin films were transparent and flexible. The lizardfish gelatin films were all slightly yellowish while the bovine gelatin films were clearer. The L value of bovine gelatin films had the highest value (P≤0.05) whereas lizardfish scale gelatin films with and without enzyme were not significantly different (P>0.05) for L, a, and b values and ΔE. The film's mechanical properties included tensile strength (TS) and elongation at break (E) were not significantly different (P > 0.05) for E and the films of lizardfish scale gelatin showed higher TS than the films without enzyme added (P ≤ 0.05). The water vapor permeability of films from lizardfish scale gelatin with and without 0.5% MTGase and bovine gelatin films were 21.0 ± 0.17, 26.3 ± 0.79, and 25.8 ± 0.09 g·mm/m(2)·d·kPa, respectively, while the oxygen transmission rate of all 3 types of films were less than 50 cc O(2)/m(2)·d.     

Quantitative detection of Plesiomonas shigelloides in clam and oyster tissue by PCR

A quantitative assay for Plesiomonas shigelloides in clams and oysters based on the conventional polymerase chain reaction was developed. The assay involved the treatment of homogenized tissue samples with 4.0% formaldehyde that presumably denatured DNases and proteases present in the tissue which would otherwise inactivate the PCR reaction. The level of detection of P. shigelloides in clam tissue without enrichment was 200 CFU/g. The addition of 0.1% bovine serum albumin (BSA) to PCR reactions or the DNA purification system reduced the level of detection to 60 CFU/g. Formaldehyde had no effect on the level of detection with clam tissue. The level of detection of P. shigelloides in oyster tissue without enrichment was 6x10(5) CFU/g. The addition of 4.0% formaldehyde to oyster tissue homogenates reduced the level of detection to 6x10(2) CFU/g in contrast to the addition of 0.1% BSA to PCR reactions or the DNA purification system which reduced the level of detection to only 2x10(5) CFU/g. The combination of formaldehyde plus BSA, formaldehyde plus DNA purification, or formaldehyde plus BSA plus DNA purification all gave a detection level of 2x10(2) CFU/g of oyster tissue. With clam tissue, the linear range for detection of P. shigelloides was 60 to 2x10(4) CFU/g. With oyster tissue, the linear range for detection of P. shigelloides was 2x10(2) to 6x10(4 )CFU/g.     

Muscle glycogen level and meat quality in pigs of different halothane genotypes

The halothane genotype of 22 Polish landrace pigs was determined using halothane test and blood typing. Eight homozygous normal (NN), eight hetero-zygotes (Nn) and six homozygous recessive (nn) were identified. The levels of glycogen and lactate were measured in biopsy samples taken from the longissimus lumborum using a shot biopsy technique. pH (pH(1)) and IMP/ATP ratio (R) were determined at 30 min after slaughter, while pH, meat colour and water holding capacity were determined on the day after slaughter. The halothane genotype did not affect intra vitam glycogen level. The nn pigs had a higher R value and lower pH(1) than both Nn and NN animals. Heterozygous animals were intermediate between both homo-zygotes for biopsy lactate level and meat colour. The lactate content of biopsy samples was significantly correlated with pH(1) (r = -0·68; P < 0·01), R (r = 0·68; P < 0·01), meat colour (r = 0·57; P < 0·01) and water holding capacity (r = 0·45; P · 0·05).     

Short communication: Feed iodine concentrations on farms with contrasting levels of iodine in milk

In a previous study, milk iodine concentration from 501 farms across Canada was found to vary considerably and appeared to be influenced by feeding practices. Farms with contrasting levels of milk iodine from a subset of 200 participating farms were used to determine the relationship between milk iodine concentration and the concentration of this mineral in different feeds and complete diets given to lactating dairy cows. The 30 farms with the lowest levels of iodine in milk (low group) and the 30 farms with the highest levels (high group) were selected. Samples of bulk tank milk, all feed ingredients, and water were collected. Additionally, each farmer completed a questionnaire providing information on feeding management. The iodine offered on each of the farms was estimated from the amount of the feed in the diet recommended by the Ration’L software (Valacta, Ste-Anne-de-Bellevue, QC, Canada) and the iodine concentration in the feed sampled and analyzed using inductively coupled plasma mass spectrometry. The dietary concentration of iodine offered daily was 33% lower for the low group compared with the high group; that is, 1.20 ± 0.099 versus 1.81 ± 0.195 mg/kg of dry matter (DM), respectively. Milk iodine concentrations averaged 146 ± 13.9 μg/kg for the low group and 487 ± 44.6 μg/kg for the high group. A linear relationship was found between dietary iodine concentration and milk iodine level, as follows: milk iodine (μg/kg) = 145 (±66.9) + 113 (±39.4) dietary iodine concentration (mg/kg DM). However, the low R² value (0.15) indicates that other factors, such as milking management and the presence of goitrogens, may have affected the concentrations of iodine in milk. Forages supplied approximately 17% of iodine requirements in the average lactating cow diet. Therefore, variations in the iodine content of forages are unlikely to cause iodine overfeeding. In contrast, 27% of the mineral mix samples presented iodine concentrations >100,000 μg/kg of DM (and up to 322,000 μg/kg of DM). More than 85% of the farms tested were feeding iodine levels higher than the dietary iodine recommendations (0.5 mg of iodine/kg of DM). Iodine supplements should be used with caution in lactating cow diets.     

Biochemical studies on fast glycolysing bovine muscle

Of the psoas major muscles from 1395 carcasses of young bulls 64% showed pH(1) values (30 min post mortem) below 6·0. In 100 muscle samples (selected so that a normal distribution of the pH(1) values was obtained), water-holding capacity (WHC), brightness of colour and the concentration of all glycolytic metabolites were determined. There were correlations between pH(1) and the other characteristics of meat quality, lower pH(1) values were associated with lower WHC, paler colour, lower glycogen levels and higher levels of lactate (30 min post mortem). All these correlations were highly significant. The accelerated breakdown of glycogen-and a simultaneous accumulation of hexose monophosphates-indicate an activation of the phosphorylase system in fast glycolysing bovine muscle. In fast glycolysing muscle, creatine phosphate was almost absent by 1 h post mortem and the ATP level was very low, indicating a high rate of breakdown of high-energy phosphates. The quality deviation of fast glycolysing beef is much less severe than that of PSE pork and therefore might not present a serious economic problem.     

Effect of reduced sodium chloride concentration and tetrasodium pyrophosphate on pH, water-holding capacity and extractable protein of prerigor and postrigor ground beef

The effect of tetrasodium pyrophosphate (TSPP) (0, 0·25, 0·5% w/w) alone or in combination with salt (NaCl) (0, 0·5, 1·0% w/w) on water-holding capacity (WHC), pH, the ratio of absorbance at 250 nm over the absorbance at 260 nm (R-values) and 150m CaCl extractable protein (EP) was studied in prerigor and postrigor sternomandibularis homogenates over time. The 0 h samples were defined as when the NaCl was incorporated with the muscle. R-values verified that 0 h samples were in a prerigor or postrigor state. In prerigor homogenates, increasing phosphate concentration increased the time required to reach ultimate pH. Ultimate pH values of prerigor homogenates containing phosphate were lower (P < 0·05) than homogenates without phosphate and similarly treated postrigor homogenates. After six hours, no differences (P > 0·10) were noted in EP or WHC at different phosphate concentrations when averaged over NaCl concentrations in prerigor homogenates. With increasing phosphate concentration of postrigor homogenates, there was an increase (P < 0·05) in pH and EP at the initial sampling time. However, 0 and 0·25% phosphate WHC values could not be differentiated (P > 0·10). Results of this study indicate no advantages, after six hours post mortem, to using TSPP alone or in combination with NaCl in prerigor meat homogenates at concentrations added in this study.