Evaluation of lean meat quality in pigs using two electronic probes

The Danish Fat-O-Meater grading probe (FOM) and the Fibre Optic Probe (FOP) developed at IFR, Bristol, were evaluated for their potential ability to predict lean meat quality in a sample of 76 pig carcasses showing a wide range of quality in the M. longissimus dorsi. When probings were made after chilling at about 20 h post mortem the correlations between probe value (FOP_u and FOM_u) and reflectance (EEL value), drip loss during storage and subjective assessment score for colour-structure were high (FOP_u and reflectance, r = 0·89; drip loss, r = 0·78; subjective assessment, r = 0·90. FOM_u and reflectance, r = 0·88; drip loss, r = 0·73; subjective assessment r = 0·81). Nevertheless, probe values could not be used to unambiguously group samples into normal, pale, soft, exudative (PSE) or dark, firm, dry (DFD) classes. Correlations between probe values at 45 min post mortem and measures of ultimate meat quality were much lower. Neither probe could potentially differentiate between normal and DFD meat at this time and differentiation between normal and PSE meat was also poorer.     

Spray chilling of lamb carcasses

Two spray-chilling treatments were developed to improve appearance and reduce weight loss during lamb chilling. Rates of cooling and weight loss and meat quality were compared to conventionally chilled carcasses.

The first treatment was an intermittent spray during the first 3 h of chilling. The second consisted of only two sprays at 2 h and 10 h post mortem. The conventional control was a two-stage process, with air at 10°C and 1 m/s up to 10 h post mortem, followed by air at 0°C and 1 m/s for a further 14 h.

Both treatments significantly reduced weight loss at 24 h post mortem compared to conventional, from 2·20% to 0·86% and 1·20%, respectively. During a further 4 days storage, the savings were maintained, with weight losses being 3·97%, 2·97% and 3·19%, respectively.

There were small (<1 h) but significantly reductions in the cooling times of spray-chilled loins and legs, attributed to sustained evaporative cooling of the continually wetted surfaces.

No effects on texture or drip loss and only slight effects on surface lean and fat colour were found. Variation in texture between animals within treatments was far greater than between treatments and could not be accounted for by variations in cooling rates.     

Sarcomere shortening and contraction nodes in stretched-restrained ovine myofibres during post mortem storage

Myofibres of muscles removed from the carcass shorten during rigor mortis. Whether myofibres of stretched and restrained muscle tissues shorten during post mortem storage was examined. Muscle strips removed from the semimembranosus muscle of sheep before rigor onset were stretched and restrained. The muscle strips were fixed separately in formalin solution from 1.5 hr to 12 days post mortem, and embedded in paraffin. Sections were stained with Mallory-azan. Some myofibres in the pre-rigor-excised and stretched-restrained muscle strips had contraction nodes at 1 day post mortem. The contraction node did not increase in frequency hereafter. Two to several successive sarcomeres shortened regularly to form the nodes parallel to the Z-line. In addition, several successive sarcomeres shortened partly and successively from one side to the other side to form the nodes oblique to the Z-line. Oblique and irregular contraction nodes appear to cause kinks or bends of myofibres. Sarcomere lengths were not always uniform in individual myofibres. Formation of contraction nodes and shortening of partial sarcomeres in the stretched-restrained myofibres indicate that the myofibres shorten individually during rigor mortis and vary in shortening states as in muscles left on the carcass.     

Impact of salt, phosphate and temperature on the effect of a transglutaminase (F XIIIa) on the texture of restructured meat

The effect of the transglutaminase F XIIIa on texture parameters was analysed in meat model systems simulating a restructured meat product. Porcine M. longissimus dorsi at normal ultimate pH was obtained 2 days post mortem from pigs slaughtered at approx. 100 kg liveweight. The F XIIIa product used was a recombinant protein produced by fermentation of Saccharomyces cereviciae. In raw minced meat F XIIIa increased cohesion, hardness and elasticity when a time-temperature heat treatment of 37 °C and 90 min was used during processing, while processing at 10 °C for 23 h caused only minor texture changes. Salt and phosphate addition together with F XIIIa resulted in a remarkable increase in binding properties. Thus, the texture parameters increased particularly at salt levels between 2 and 4% and a phosphate level of 0.2%. Binding of meat pieces containing 0.2% phosphate, 1% salt and F XIIIa as 0.4% active enzyme to substrate showed significant effect on the tensile strength compared to the samples without F XIIIa, however, color deterioration of the product was observed when adding F XIIIa.     

The influence of high temperature, type of muscle and electrical stimulation on the course of rigor, ageing and tenderness of beef muscles

The course of rigor mortis (rigor), ageing and tenderness has been evaluated for three beef muscles; M. biceps femoris (BF), M. semimembranosus (SM) and M. semitendinosus (ST), when entering rigor at constant temperatures of 15 and 37°C respectively, with and without electrical stimulation (ES/NS) (85 V, 14 Hz and 32 s). The course of post-mortem changes has been registered by isometric tension, by shortening of unrestrained muscle strips and by following the pH decline and the changes in metabolites, such as ATP and CP. Ageing at +4°C was recorded by measuring Warner-Bratzler (W-B) shear values 2, 8 and 15 days post mortem. On the last occasion, the sensory properties of the cooked meat were also evaluated. Maximum shortening and isometric tension were higher at 37°C as compared to 15°C, whereas ES did not reduce rigor shortening. A high correlation between maximum shortening and the ATP-level at the onset of the shortening rapid phase was found (r = 0·77(???)), which could explain the greater shortening obtained at 37°C compared to 15°C. Rigor shortening is an important phenomenon governing meat tenderness as tenderness is highly affected by rigor temperature but not by ES. This was the case for muscles SM and ST but not for BF muscle. Even though tenderness was measured after ageing (15 days post mortem), shortening during rigor seems to be more important for toughness when rigor mortis occurs at 37°C than any suggested tenderizing effect due to increased proteolysis in this temperature region.     

Effect of rigor temperature on muscle shortening and tenderisation of restrained and unrestrained beef m. longissimus thoracicus et lumborum

Pairs of muscularis longissimus thoracicus et lumborum (LTL) from young bulls were removed within 1h of slaughter. Small portions of the muscles were placed in a rigormeter to continously follow the isometric tension and isotonic shortening developed, at constant temperatures of 15, 20, 25, 30 and 35°C, as the muscle went into rigor. The bulk LTL was placed in water baths at the same temperature. One of the bulk pairs was tightly restrained by wrapping, to reduce muscle shortening, the other was unrestrained free to shorten. For the bulk samples, shear values were measured using a Warner-Bratzler instrument (1, 7 and 14 days post mortem), and sensory attributes were measured using a sensory panel (7 and 14 days post mortem). Minimum tension and shortening occurred at 15°C. The activation energy for the muscle shortening process was larger than for the isometric tension process. This indicates that the isometric tension data, collected during rigor, does not solely reflect muscle shortening. Thus, a counteracting process that decreases the tension response, most likely ageing is simultaneously detected. Meat that went into rigor at 15°C had least shortening and was always more tender than meat going into rigor at higher temperatures. For meat entering rigor at temperatures higher than 15°C, restraining of the muscle by wrapping, significantly (p<0.05) decreased the amount of muscle shortening and resulted in an improved meat tenderness (p<0.001). It was also observed that at rigor temperatures higher than 15°C the meat tenderness is affected negatively by a reduced ageing capacity. It therefore appears that muscle shortening and enzyme activity both affect tenderness and that both are highly affected by rigor temperature and have the greatest beneficial effect at a rigor temperature of 15°C.     

Sarcomere shortening of prerigor muscles and its influence on drip loss

Detailed studies of muscle shortening post mortem at incubation temperatures between −2°C and +38°C revealed that the sarcomeres in unrestrained, excised red bovine muscle (M. sternomandibularis) shortened less than 10 % in the prerigor state between 6°C and 18°C. Below 6°C, sarcomeres contracted up to 70%. Between 20°C and 38°C sarcomere shortening of 40% was observed. In the red porcine M. cleidooccipitalis the minimum of shortening was measured at about 10°C, a higher degree of shortening—up to 50%—being obtained above and below this temperature. The drip loss of both muscle types increased linearly with increasing prerigor shortening.

This latter relationship is discussed with regard to changes within the muscle post mortem. The influence of three events on water movement from the interfilamental space into the interfibrillar fluid and from there into the extracellular space is critically evaluated. These events are: (1) the prerigor contraction of sarcomeres depending on the temperature of storage, (2) the changes due to the falling pH post mortem and (3) the onset of rigor mortis, with its irreversible association of actin and myosin.     

Effect of meat ultimate pH on rate of titin and nebulin degradation

The processes involved in the tenderisation of meat were studied on muscles with a range of ultimate pH values (5.4–7.0), produced by subcutaneous injection of various doses of adrenaline and exercise. The m. longissimus thoracicum et lumborum (LD) was removed from carcasses stored at 10 °C and held for 1, 3 or 6 days after slaughter, then frozen until tenderness assessment. The tenderness of meat cooked from the frozen state was determined as the force to shear samples of 10 mm × 10 mm cross-section using a MIRINZ tenderometer. The maximum toughness of 15 kgF occurred at an ultimate pH (pH_u) of about 6.0, resulting in a curvilinear relationship between tenderness and pH_u at 1 day post-slaughter. By 6 days post-slaughter, all meat had reached the same low shear value of approximately 3 kgF. SDS-PAGE patterns obtained from samples at 12, 24 and 48 hr post-slaughter showed increasing titin and nebulin degradation over time, with the slowest rate of degradation occurring at pH_u values 6.0–6.3. Titin and nebulin are known to play an important role in the stabilisation of myofibril structure, and it is suggested that the curvilinear relationship results when pH-dependent titin and nebulin degradation occurs.     

Colour of normal and high pH beef heated to different temperatures as related to oxygenation

The effects of oxygenation and thermal treatment (internal temperature, T_i: 45, 60, 75°C) on the colour and some colour related physical and biochemical properties of beef longissimus dorsi (LD) muscle, both normal (pH_u5.6) and DFD (pH_u>6.6), were studied. The colour components (L^*, a^*, b^* values) for the raw and heated LD, both before and after oxygenation, were instrumentally and sensorily evaluated. The colour of raw and heated (60°C) DFD beef before and after oxygenation differed significantly from the normal meat and contained more native muscle pigment (TMP). pH also influenced the depth of the oxygenated layer, specific activity of cytochrome c oxidase (SACCO) and the amount of oxygen consumed. An increase in internal temperature was usually accompanied by a lower SACCO and a significant decrease of TMP, as well as a change of all colour parameters. Oxygenation of the raw and heated slices (except at 75°C) of both types of meat led to higher L^*, a^* and b^* values.     

The effects of spray and blast-chilling on carcass shrinkage and pork muscle quality

Combinations of blast- and spray-chilling of pork carcasses were compared to spray-chilling at conventional chilling temperatures with regard to carcass shrinkage during chilling and pork muscle quality. In experiment 1, pork sides were spray-chilled at 1°C for the first 10 h (40 spray cycles of 60-s duration every 15 min) of cooling or blast-chilled at −20°C for 1, 2 or 3 h followed by spray-chilling for 9, 8 or 7 h duration, respectively. All pork sides were then chilled to 24 h post mortem at 1°C. Experiment 2 followed the same procedures as experiment 1, except that −40°C was used as the blast-chill temperature.

Carcass shrinkage was similar for all treatments in experiment 1 at 24 h ranging from 0·5–0·7 g 100 g⁻¹. Blast/spray-chilling increased the rate of chilling and reduced the rate of post-mortem pH decline in two muscles (longissimus thoracis, LT and semimembranosus, SM) compared to the combined conventional/spray-chill treatment. Carcasses that were blast-chilled for 3 h had LT muscles that were darker with a higher protein solubility, less drip loss, shorter lengths and higher shear values compared to those from carcasses in the conventional/spray-chill treatment. In experiment 2, carcasses blast-chilled for 3 h at −40°C recorded a weight gain at 24 h of 0·4 g 100 g⁻¹, compared to a weight loss in all other treatments (0·2–0·4 g 100 g⁻¹). Muscle colour was darker in both the LT and SM of carcasses blast-chilled for 3 h at −40°C compared to carcasses from the conventional/spray-chill treatment, but most other measurements of muscle quality showed an inconsistent response to chilling treatment.     

Comparison between two statistical models for prediction of turkey breast meat colour

The aims of the present study were: (1) to determine the relevant objective measurements which could express visual assessment of turkey meat colour; and (2) to use these variables for the early prediction of the colour development of turkey breast meat.

The colour of the meat was assessed subjectively by an expert at a processing plant at 24 hr post mortem, using a four-category scale (score a: light-pale meat, score b: light pink meat or normal meat, score c: dark meat, score d: very dark meat).

Objective measurements included meat pH, temperature, dielectric loss factor, pigment concentration, L^* (lightness), a^* (redness) and b^* (yellowness) colour coordinates determined at different times post mortem.

Colour coordinates and pH were chosen as relevant variables when measured at 1 and 4 hr post mortem and were used in prediction models. Linear analysis (canonical discriminant analysis) showed that the efficiency of prediction was 15%. A non-linear analysis (neural network) gave better prediction; the colour of the meat being correctly predicted for 70% of the muscles.     

Peptides in rainbow trout (Oncorhynchus mykiss) muscle subjected to ice storage and cooking

Although proteolysis during post mortem storage is an important factor affecting fish texture, little is known about degradation end-products. This study was performed to investigate the occurrence of low molecular weight peptides (<5 kDa) in post mortem rainbow trout muscle, during ice storage, and to evaluate their stability during cooking. It combined quantitative (amino acid analysis) and qualitative approaches (mass spectrometry). The results showed that muscle of trout was poor in peptides. These were mainly anserine and glutathione. Their concentration was almost unaffected by the seven days of ice storage and vacuum cooking for 5 min at 70 °C. MS analysis revealed a limited but highly reproducible appearance of small peptides in trout muscle during the ice storage and after cooking. The compounds detected by MS analysis remain to be characterised.     

The relationship of muscle fibre size to tenderness of beef

Steaks were removed from loins of beef carcasses at 1, 3, 6 or 14 days post mortem for fragmentation index (MFI), Warner-Bratzler Shear Force (SF) and sensory panel tenderness evaluation. Also, after 1 day of storage, samples were removed for histological observations. Greatest improvement in tenderness, SF and MFI occurred within the first 6 days of storage. Sensory panel tenderness was correlated (P < 0·01) with SF and MFI. Average muscle fibre size was correlated (P < 0·01) with tenderness and SF at days 1 and 3, but not at days 6 and 14. Evidently, muscle fibre size is important to tenderness prior to post-mortem storage of meat and proteolysis, but becomes less of a factor in tenderness after 6 days of storage.     

Post mortem evolution of myofilament spacing and extracellular space in veal muscle

The post mortem evolution of water distribution was studied in muscle tissue from veal calves in two experiments. Myofilament spacing, extracellular space and rate and extent of pH fall were determined in Psoas major muscle in Experiment 1. Extracellular space and rate and extent of pH fall were determined in Longissimus dorsi, Psoas major and Trapezius muscles in Experiment 2. In Experiment 2, the variability of ultimate pH was increased by using adrenalin injections. The myofilament spacing decreased after slaughter when pH reached values around 5·9. In both experiments, the extracellular space began to increase soon after slaughter in close relation with the pH changes. The size of the ultimate extracellular space was significantly correlated with the rate of pH fall, but not with the ultimate pH.     

Dietary creatine monohydrate affects quality attributes of Duroc but not Landrace pork

Increased creatine content in the muscle may delay post mortem lactate formation and postpone the pH decline, hence potentially improving the water-holding capacity (WHC). Duroc and Landrace pigs were supplemented with 0, 12.5, 25 or 50 g creatine monohydrate (CMH)/d for 5 days prior to slaughter. Meat from Longissimus dorsi (LD) of Duroc pigs had a higher WHC and pH at all times, lower colour determinants; a* (redness), b* (yellowness), L* (lightness) and was more juicy compared to that of Landrace pigs. Furthermore, higher pH_2 h, pH_24 h and decreased colour determinants were observed in carcass sides exposed to a faster cooling profile. Dietary supplementation with CMH increased the body weight gain of both breeds. However, only meat from Duroc pigs had higher pH_30 min and pH_45 min (at 50 g CMH/d) and WHC, but reduced redness (reduced in both breeds) and juiciness when supplemented with CMH compared to non-supplemented controls.     

An investigation of ultimate pH in the muscles of commercial beef carcasses

Ultimate pH values were recorded in the carcasses of steers and heifers at a beef slaughtering plant over a period of 3 years. The incidence of carcasses with a pH_u ≥ 6·0 in the LD—a value usually associated with ‘dark-cutting’ in beef—was 3·2%. A pronounced seasonal effect was observed with the incidence rising from 1·2% for the period February to August to 5·2% for the period September to January, inclusive. An examination of thirteen muscles showed that increases in pH_u above normal values occurred most frequently in the LD and four large muscles of the hindquarter and were much less frequently observed in the eight other hind- and forequarter muscles examined. In the carcasses of young bulls, also slaughtered under commercial conditions, high pH_u values were predominantly associated with the same muscles as in steers and heifers. However, when experimental cattle were given adrenaline to induced high pH_u values, this treatment resulted in a general increase in pH_u in all the muscles examined. The different pattern of pH_u elevation in the adrenaline-treated and commercial carcasses suggests different physiological mechanisms in the two cases.     

Effects of rigor temperature and electrical stimulation on venison quality

The effects of rigor temperature and electrical stimulation on venison quality were assessed using venison longissimus dorsi muscle. In the first trial, effect of rigor temperature (0, 15, 25, 30, 35 and 42 °C) and time post-mortem (at rigor, 3, 7 and 14 days) on drip and cooking losses, % expressible water (water holding capacity, WHC), sarcomere length, protein solubility, meat tenderness and colour were investigated. In the second trial, the effects of rigor temperature (15 and 35 °C), electric stimulation (stimulated or not stimulated) and time (at rigor, 3 and 6 weeks post-mortem) on tenderness and colour were further investigated. Results of the first trial showed no clearly established trends of the effect of rigor temperature and time on the cooking and drip losses and protein solubility except venison muscles that went into rigor at 42 °C tended to have higher drip loss and lower protein solubilities compared to muscles that went into rigor at the other temperatures. Venison water holding capacity (WHC) decreased with the increase in rigor temperature (P < 0.001) and venison became more tender with time post-mortem. Venison colour improved with increasing rigor temperature. During display, samples that went into rigor at 15, 25 and 35 °C had the lowest and those at 0 and 42 °C had the highest rate of change of redness (a^*) value with time. In the second trial, tenderness was improved by stimulation (P = 0.01). Redness (a^*) values were affected by rigor temperature (P < 0.01) and post-mortem time (P < 0.001) but not by electrical stimulation. It is concluded that venison tenderness can be improved via the manipulation of rigor temperature to obtain acceptable level of tenderness early post-mortem with less damaging effect on colour stability.     

Modeling the effect of inoculum size and acid adaptation on growth/no growth interface of Escherichia coli O157:H7

The objective of this study was to model with logistic regression the growth/no growth interface of different initial inoculation levels (10¹, 10³ and 10⁵ CFU/ml; study 1), or nonadapted vs acid-adapted (study 2) Escherichia coli O157:H7 as influenced by pH, NaCl concentration and incubation temperature. Study 1 was conducted with a mixture of four E. coli O157:H7 strains grown (35 °C, 24 h) in tryptic soy broth (TSB). Study 2 was conducted with the same mixture of four E. coli O157:H7 strains grown (35 °C, 24 h) in glucose-free TSB with 1% added glucose (final pH 4.83), or in diluted lactic acid meat decontamination runoff fluids (washings; final pH 4.92), or nonadapted cultures prepared in glucose-free TSB (final pH 6.45), or in water washings (final pH 6.87). Parameters included incubation temperature (10–35 °C), pH (3.52–7.32), and NaCl concentration (0–10% w/v). Growth responses were evaluated for 60 days turbidimetrically (610 nm) every 5 days in 160 (study 1) and 360 (study 2) combinations in quadruplicate samples, with a microplate reader. The lower the initial inoculum the higher were the minimum pH and a_w values permitting growth. Differences in the pH and a_w growth limits among inoculum concentrations increased at 15 and 10 °C. Acid-adapted cultures were able to grow at lower pH than nonadapted cultures, while at temperatures below 25 °C, growth initiation of nonadapted cultures stopped at higher a_w compared to acid-adapted cultures for the whole pH range of 3.52 to 7.32. A comparison with available data indicated that our model for acid-adapted E. coli O157:H7 in different environments may provide representative growth probabilities covering both nonadapted and stress-adapted contaminants.     

Effect of temperature and water activity on growth and ochratoxin A production by Australian Aspergillus carbonarius and A. niger isolates on a simulated grape juice medium

The effect of water activity (0.92, 0.95, 0.965 and 0.98) and temperature (15 °C, 25 °C, 30 °C and 35 °C) on growth rate and ochratoxin A (OA) production by five strains of Aspergillus carbonarius and two strains of A. niger isolated from Australian vineyards was characterised on a synthetic grape juice medium. Maximum growth for A. carbonarius occurred at ca 0.965 a_w and 30 °C, and for A. niger, at ca 0.98 a_w and 35 °C. The optimum temperature for OA production was 15 °C and little was produced above 25 °C. The optimum a_w for toxin production was 0.95–0.98 for A. carbonarius and 0.95 for A. niger. Toxin was produced in young colonies after and, typically, did not continue to accumulate the entire surface area of the plate was colonised. Rather, the amount decreased as colonies aged. Trends for growth and OA production were similar among Australian isolates and those from European grapes, as reported in the literature.     

Changes affecting the Longissimus dorsi, Triceps brachii caput longum and Rectus femoris muscles of young Friesian bulls during meat ageing

The chemical composition and post-mortem changes during 3–14 days of ageing were studied on three muscles (Longissiums dorsi, Triceps brachii caput longum, Rectus femoris) from 13 young Friesian bulls. Chemical composition varied widely between animals (p < 0.001) and muscles (p < 0.001), and did not change during post-mortem storage. Significant changes affecting the non-protein nitrogen and soluble protein nitrogen contents were similar in all three muscles but differed from animal to animal. The increase in non-protein nitrogen can be considered as an indicator of proteolysis. Proteolysis extended to 14 days post mortem. The myofibril fragmentation index increased significantly (p < 0.001) between 3 and 7 days post mortem along the same pattern, irrespective of the muscle and animal. A ceiling was reached at around 7 days post mortem, by which time maximum breakdown of the structure had probably occurred.

No significant relationship was observed between chemical composition, changes in the soluble protein nitrogen, breakdown of structures and carcass characteristics.