Manipulation of the pre-rigor phase to investigate the significance of proteolysis and sarcomere length in determining the tenderness of bovine M. longissimus dorsi

The objective of this study was to evaluate the importance of proteolysis and sarcomere length in determining the tenderness of bovine M. longissimus dorsi (LD) muscle over a 21-day period. This was done by altering the pre-rigor glycolytic behaviour of hot-boned LD muscles using different early post-mortem temperature regimes. Hot-boned LD muscles (n=8) were cut in two, randomised, placed in polythene bags and submerged in a water bath set at 5°C (rapidly chilled) and 15°C (slowly chilled) for 8h post-mortem. All muscles were then stored at 2°C for up to 21 days post-mortem. The temperature regimes altered the glycolytic behaviour of the muscles in the pre-rigor period. The slowly chilled muscles exhibited a faster (P<0.01) pH fall than rapidly chilled muscles. Cold shortening was induced in rapidly chilled muscles as they had shorter (P<0.01) sarcomere lengths than slowly chilled muscles up to day 21 post-mortem. Warner Bratzler shear force values (WBSF) deemed cold-shortened muscles as tougher than noncold shortened up to day 14 post-mortem. Both cold-shortened and noncold-shortened muscles tenderised over time to an extent where there was no significant difference in WBSF values by day 21 post-mortem. SDS-PAGE protein profiles indicated that the rate of proteolysis was faster in slowly chilled muscles when compared to rapidly chilled muscles. However by day 21 post-mortem it appeared that rapidly and slowly chilled muscles underwent proteolysis to the same extent.     

Effect of very fast chilling and aging time on ultra-structure and meat quality characteristics of Chinese Yellow cattle M. Longissimus lumborum

Objectives of the current study were to evaluate meat ultra-structure and tenderness variation at different chilling regimes and aging times. Hot boned longissimus lumborum of 18 Chinese crossbred cattle were divided into 4 portions per side. One portion underwent very fast chilling (VFC, at -21°C to achieve core temperature of 0°C, then transferred to another incubator at 2°C), whereas other treatments were held at 14, 7 and 0°C for 10h postmortem, respectively. At 10h postmortem, all muscles were vacuum aged at 2°C for 21d. Cold shortened muscles had greatest absolute amount of tenderization during aging. VFC caused lowest sarcomere length, with super-contractions, ruptured Z-lines and myofibril cleavage, but improved myofibril fragmentation index (MFI), with no significant negative effect on toughness. Overall, aging improved the meat quality of cold shortened beef. Moreover, it should be prudent in some applications to apply VFC to excised muscles from a food safety perspective, and to improve tenderness compared to cold-shortened muscles.     

Effects of electrical stimulation, chilling temperature and hot-boning on the tenderness of bovine muscles

The objective of this study was to determine the effects of hot-boning, low voltage electrical stimulation (ES) and chilling temperature on the tenderness of bovine M. longissimus dorsi (LD) and M. semimembranosus (SM) muscles. LD (n=32) and SM (n=32) muscles were subjected to different post-mortem treatments; hot-boning (before 90min post-mortem), cold-boning (at 48h post-mortem), low voltage ES and rapid or slow chilling. Hot-boned muscles which were not electrically stimulated (NES) had higher Warner Bratzler shear force (WBSF) values (P<0.001) and shorter sarcomeres (P<0.001) than cold-boned muscles. Hot-boned muscles subjected to ES had lower pH values (P<0.001) post-stimulation and up to 8h post-mortem than NES muscles. At both chilling temperatures WBSF values were lower in ES hot-boned LD and SM muscles at days 2, 7 and 14 post-mortem than NES muscles. Hot-boned muscles subjected to slow chilling had longer sarcomeres (P<0.001) than those subjected to fast chilling. In hot-boned SM muscles, ES resulted in longer sarcomere lengths (P<0.001). However, ES did not have a significant effect on the sarcomere length of LD muscles. As indicated by WBSF values all muscles tenderised during ageing, including muscles which were 'cold shortened'. Proteolysis was not the main reason for differences in WBSF values between ES and NES muscles as judged by qualitative sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). A combination of slow chilling and ES had a positive effect on hot-boned muscles with respect to WBSF values.     

The effect of cooling rate on beef tenderness: The significance of pH at 7 °C

To study the effects of cooling regime on beef tenderness, seven commercial beef slaughterhouses with different cooling regimes were selected to obtain different carcass cooling rates. The pH values and temperatures of 8 M. longissimus dorsi (LD) and M. semimembranosus (SM) muscles from each slaughterhouse were monitored for 30 h. The muscles of the monitored carcasses were excised and vacuum packed for Allo-Kramer shear force (SF) determinations. Samples were kept at 3-4 °C for 5 or 21 d. The slaughterhouses were grouped by their average pH values of the muscles, prevailing at the moment when the temperature of the muscles reached 7 °C. The pH groups for LD were (i) low (5.52-5.63), (ii) medium (5.84-5.97) and (iii) high (6.16-6.17). The highest shear forces were in group (iii), being the toughest: 155-152 N/g, and the lowest in group (i) (the most tender): 108-116 N/g, respectively. The regression equation or the shear force was SF=-295.4+73.0?(pH at 7 °C); (R(2)=87%). There was no significant correlation between the cooling rate and tenderness in SM, indicating that it is difficult to control the tenderness of all muscles using the same cooling regime. The ageing effect was more marked and the variation in the shear forces smaller in the slaughterhouses generating carcasses with low pH values at 7 °C than in those generating high ones. It was concluded that a low cooling rate, or more specifically, the temperature/pH at the onset of rigor mortis, is important for beef tenderness. The pH of LD must fall to values below 5.7 before/when the temperature reaches 7 °C.     

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.     

Ultrastructural Variation in Beef M. longissimus dorsi as an Explanation of the Variation in Beef Tenderness

ABSTRACT: The objective of this experiment was to quantify variation in bovine M. longissimus dorsi tenderness and determine the extent such variation is explained by variation in the ultrastructure of muscles after different postmortem treatments. Eight muscles were hot-boned and aged for 2 d at 2 °C (T1) to achieve very contracted actomyosin crossover and tough beef. Eight carcass sides were tenderstretched for 10 h at 10 °C and a further 38 h at 2 °C (T2) to achieve lengthened actomyosin crossover and tender beef. Both T1 and T2 were compared with conventionally hung carcasses, which underwent similar chilling regimes, C1 ( n = 8) and C2 ( n = 8), respectively. Measurements of sarcomere length, pH, Warner Bratzler shear force (WBSF), and sensory tenderness were taken, and transmission electron microscopy images analyzed. Variances of attributes were analyzed on Bartlett's test. Variances of the 4 groups were homogenous for all attributes except for pH after 24 h postmortem (with T1 [0.00] having lower variances than C1 = 0.04, T2 = 0.06, and C2 = 0.05) and WBSF after 2 d aging (with T2 [74.33] having lower variances than T1 = 236.76, C1 = 398.82, and C2 = 856.74). The variation in the tenderness of beef was quantified through ultrastructural variation in bovine muscle, with tenderstretched moderately chilled beef having the least variable tenderness as a result of more uniform overlap between actin and myosin filaments. Variation in the eating quality of beef was not reduced by hot-boning with fast chilling or conventional hanging with fast or moderate chilling. The development of the uniformity within filaments of tenderstretched muscle requires further analysis as residual variation remains.     

The influence of biochemical differences on the variation in tenderness of M. longissimus dorsi of Belgian Blue steers managed homogenously pre and post-slaughter

The objective of this experiment was to determine the contribution of some biochemical processes of postmortem muscle to the variation in tenderness of beef from Belgian Blue bull cross Holstein-Friesian steers (n=10). These animals were managed optimally from conception to consumption with the aim of reducing tenderness variation. The M. longissimus dorsi (LD) from the left hand side (LHS) and the right hand side (RHS) were analysed for variation in tenderness using Bartletts test. The quality measurements included pH, temperature, Warner Bratzler shear force, sensory tenderness, chemical composition and sarcomere length. Biochemical measurements included myofibrilar proteolysis, glycolytic potential, adenine/inosine ratio and collagen content. No difference for variances or means were observed between LHS and RHS for chemical, quality or biochemical attributes. Biochemical variation was greater than the variation observed in most of the quality attributes measured. Proteolysis was the main biochemical contributor to the variation in shear force tenderness after 2 and 7 as postmortem, but not sensory tenderness. Glycolysis levels and adenine/inosine ratio explained much of the variation in sensory tenderness, but not WBSF. Collagen content in the LD muscles did not explain variation in shear force or sensory tenderness. This would suggest biochemical variation is one of the main contributors to variation in tenderness of beef managed optimally pre- and post-slaughter.     

Inhibition of the proliferation of myeloma cells by the meat origin strain Enterococcus faecium CH3

Sides of 31 non-stimulated carcasses of young bulls were subjected to the muscle stretching methods Tenderstretch (TS) by pelvic bone suspension or Tendercut (TC) with two skeletal cuts or served as controls by traditional Achilles tendon suspension. The sides were chilled at fast and medium rates, resulting in temperatures of 4-5 and 9°C in the m. longissimus dorsi (LD) at 10 h post mortem. The LDs were examined for sarcomere length, Warner-Bratzler peak shear force and sensory properties after 8 days of ageing at 4°C. At the fast chilling rate, TS and TC increased sarcomere lengths, reduced shear force and improved sensory tenderness of the LDs compared to the controls (P<0.05). At the medium chilling rate, sarcomere lengths increased (P<0.05), but no significant differences were found in shear force or sensory tenderness (P>0.05) of the muscles due to stretching. However, the medium chilling rate was efficient in producing tender LDs without applying muscle stretching methods. TS and TC are feasible alternatives for improving overall tenderness and reducing variation in tenderness of beef LD at cold shortening chilling conditions.     

Effect of calcium infusion on tenderness and ageing rate of pork m. longissimus thoracis et lumborum after accelerated boning

The effect of calcium chloride infusion at either 0.5 or 6 h post slaughter on tenderness, ageing rate and meat quality of pork longissimus muscle that had been boned at rigor or had undergone accelerated processing and conditioning at either 0?°C or 14?°C was investigated. The time of calcium infusion had no effect on the initial WBSF values or the aging rate. However, calcium infusion overall resulted in lower WBSF initially (1-day post-mortem) and also after 6 days ageing at 2?°C regardless of the processing procedures used. Calcium infusion did not, however, increase the ageing rate compared to comparable treatments that had not been calcium infused. Based on this observation and the myofibrillar fragmentation index results, it was concluded that the increased tenderness due to calcium infusion was not due to increased proteolysis as has been previously postulated, but was due to either a direct effect of calcium on tenderness, or an indirect effect of calcium via increased post-mortem glycolysis and pH decline rate resulting in reduced cold shortening. Calcium infusion had detrimental effects on drip loss and meat colour.     

Predictors of Beef Tenderness: Development and Verification

Equations were developed to predict beef longissimus dorsi (LD) tenderness after postmortem refrigerated aging. Warner-Bratzler shear force (WBSF) and myofibril fragmentation indices (MFI) were determined at 1, 3, 7 and 14 days postmortem on LD of Angus-Hereford (AH, n = 8) and 5/8 Brahman crossbred (n = 8) heifer carcasses. Correlation coefficients between WBSF and MFI were ?0.91, ?0.74, ?0.63, and ?0.40 at 1, 3, 7 and 14 days postmortem, respectively. None of the traits measured correlated significantly with 14-day WBSF (P > 0.05). A three-variable prediction equation that included 24-hr calcium-dependent protease (CDP) inhibitor activity, 0-hr CDP-I activity and 24-hr cystatin activity accounted for 63% of the variation in 14-day WBSF.     

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

The course of rigor mortis, ageing and tenderness have been evaluated for two beef muscles, M. semimembranosus (SM) and M. longissimus dorsi (LD), when entering rigor at constant temperatures in the cold-shortening region (1, 4, 7 and 10°C). The influence of electrical stimulation (ES) was also examined. Post-mortem changes were registered by shortening and isometric tension and by following the decline of pH, ATP and creatine phosphate. The effect of ageing on tenderness was recorded by measuring shear-force (2, 8 and 15 days post mortem) and the sensory properties were assessed 15 days post mortem. It was found that shortening increased with decreasing temperature, resulting in decreased tenderness. Tenderness for LD, but not for SM, was improved by ES at 1 and 4°C, whereas ES did not give rise to any decrease in the degree of shortening during rigor mortis development. This suggests that ES influences tenderization more than it prevents cold-shortening. The samples with a pre-rigor mortis temperature of 1°C could not be tenderized, when stored up to 15 days, whereas this was the case for the muscles entering rigor mortis at the other higher temperatures. The results show that under the conditions used in this study, the course of rigor mortis is more important for the ultimate tenderness than the course of ageing.     

Effect of delay time before chilling on toughness in pork with high or low initial pH

Paired M. longissimus dorsi muscles from 56 carcasses of Danish Landrace and Yorkshire breeds, slaughtered at approximately 90 kg live weight, were utilized to study the potential of cold induced toughness in pork. Based upon the pH value 45 min post stunning, the carcasses were divided in two groups: a low (5·7 ≤ pH < 6·1) and a high one (6·1 ≤ pH ≤ 6·5). The effects on Warner-Bratzler shear force, sarcomere length and myofibril fragmentation of inserting a delay time of 0, 2 and 4 h before carcasses entered the chilling tunnel (operating at -28°C to -22°C) were investigated on early excised muscles as well as on muscles removed 30 h post stunning. The left LD muscle from each carcass served as a control while all right sides were used for treatments. pH and temperature measurements obtained from LD muscles left on carcasses during chilling showed that LD muscles belonging to the high pH group involve a risk of cold shortening even when a 2 h delay was used before passing in to the chilling tunnel. Comparing pH groups, however, sarcomere lengths did not differ in control sides whereas the Warner-Bratzler shear force values were significantly higher in LD muscles taken from the high pH group. Early excision of the LD muscle resulted in shorter sarcomere lengths and increased WB shear force only for carcasses belonging to the high pH group, which, however, could be avoided by introducing a 4 h delay time before rapid chilling. The effect of delay time on tenderness from muscles excised from the carcass 30 h post stunning was much less but a 4 h delay did significantly (P < 0·05) improve tenderness in carcasses with high initial pH. Coefficient of correlation between Warner-Bratzler shear force and sarcomere length was -0·12 and nonsignificant in the low pH group, whereas it was -0·57 and highly significant in the high pH group.     

The effects of various post-mortem treatments on certain physical and sensory properties of three different bovine muscles

Sixty crossbred steers with chronological ages approximating 15 months, carcass weights approximating 270 kg and subcutaneous fat thickness measurements approximating 1·2 cm, were maintained for approximately 210 days on a constantly increasing concentrate ration (13 to 75%, according to NAS nutrient requirements for beef cattle; NAS, 1976). These animals were utilized to evaluate the effects of delayed chilling, hot-boning and electrical stimulation on certain physical, histological, biochemical and sensory properties of three different muscles (Semimembranosus, SM; Longissimus dorsi, LD; and Triceps brachii, TB). Results indicated that neither delayed chilling nor electrical stimulation produced consistent meaningful alterations in any of the physical, cooking or palatability attributes evaluated. However, early post-mortem excision of muscle (hot-boning) consistently produced toughening in all of the muscles evaluated. This was observed to a much greater degree in the TB than in either the SM or LD. Based upon sarcomere length determinations, such toughening could be attributed to cold shortening only in the TB. Electrical stimulation of excised muscle was ineffective in preventing or offsetting this toughening. The delayed chilling treatment imposed (2 h at 12·5°C) was ineffective in enhancing potential effects of electrical stimulation on tenderness.     

Calpain-calpastatin and toughness in M. longissimus from electrically stimulated lamb and beef carcasses

Shear strength, pH, temperature, μ-calpain, m-calpain and calpastatin levels were measured over a two-week post-slaughter period in Longissimus lumborum et thoracis (LD) from six lamb and six beef carcasses. All carcasses were subjected to high voltage electrical stimulation. The toughness of the beef LD determined by a MIRINZ tenderometer at 24 h post-slaughter showed a strong correlation (r=0.91) with pH of the LD at 3 h. Beef LD toughness at 14 days was correlated (r=0.84) with initial m-calpain levels. In both lamb and beef, LD toughness at 4 and 14 days respectively was also correlated with initial levels of calpastatin (r=0.85, 0.83, respectively). The strong correlation between calpastatin and the rate of tenderisation indicates that the calpain system is closely linked to the proteolytic breakdown of myofibrillar proteins. There is also evidence of an interaction between pH and μ-calpain activity. The μ-calpain, m-calpain, calpastatin, pH and temperature kinetic changes which occurred during the post-mortem ageing of beef and lamb LD were applied to a computer program which predicted rate of meat tenderisation by calculating in situ calpain activity. The closeness of fit between the predicted rate of meat tenderisation and the observed tenderness values of beef and lamb LD indicates that the post-mortem activity of μ-calpain is the major determinant of variations in tenderness. However, application of the meat tenderisation predictive program to LD from individual animals revealed that the program was not sufficiently robust for this use.     

Bovine muscle shortening and protein degradation after electrical stimulation, excision and chilling

Electrical stimulation-dependent improvement in beef tenderness resulted from mechanisms other than avoidance of cold shortening in excised muscle chilled at a normal rate (10°C at 10h post-stimulation). At normal chilling rate, electrical stimulation enhanced degradation of the myofibrillar proteins, alpha actinin and troponin-T, and increased the amount of a 30 000 dalton protein, as assessed by gel electrophoresis, whereas sarcomere lengths were not different from unstimulated muscle. Under slightly accelerated chilling conditions (10°C at 5 h post stimulation), electrical stimulation prevented cold shortening but the meat was more tender than, and had the same sarcomere length as, unstimulated muscle chilled to 10°C in 10 h. Electrical stimulation did not improve the tenderness of beef chilled at a rapid rate (10°C at 2 h post stimulation), nor did it prevent cold shortening when muscles were chilled rapidly.     

Biochemical and Quality Characteristics of Ovine Muscles as Affected by Electrical Stimulation, Hot Boning, and Mode of Chilling

The combined effects of electrical stimulation and carcass holding temperature were evaluated on some biochemical and quality characteristics of intact and hot-boned ovine muscles. Twenty-four lamb sides were randomly assigned to four treatments. Electrical stimulation was performed within 15 min postmortem (350 V with 10 Hz) for 4 min. Electrically stimulated and slowly chilled (5 hr at 14 ± 2°C) sides significantly exhibited more rapid pH decline in the longissimus dorsi (LD) muscle, less cold shortening in the semitendinosus (ST) muscle and greater tenderness in both LD and ST muscles than sides chilled at 2°C. None of the treatments had any effect on cooking loss in ST and LD muscles, lean color of LD muscle during a 4-day retail display, and solubility of different protein fractions as well as the swelling factor of the stroma protein of LD muscles.     

The effect of DFD classification and internal cooking temperature on certain pork muscle characteristics

The data incorporated in this experiment were gathered from 14 littermate pairs of swine of the same sex differing in weight by <4·5 kg with one animal in each pair subjected to standardized stress. Samples of the Longissimus dorsi (LD) and the Psoas major (PM) muscles were cooked to internal temperatures of 64, 70 and 76°C. The samples of the Quadriceps femoris (QF) muscle were cooked to internal temperatures of 70 and 76°C. DFD classification of the raw muscle was determined by the 48 h pH. Stress produced DFD meat in the PM and QF muscles but not in the LD muscle. DFD muscle required shorter time to reach any of the cooked internal temperatures studied when compared to normal muscle. Slightly-DFD PM muscle more closely resembled the normal muscle in all variables except the panel tenderness score. Cooking DFD PM muscle to an internal temperature 6°C higher than normal muscle caused a reverse in the direction of cooking loss, fiber diameter, tenderness and expressible water when compared to normal and DFD muscle cooked to the same internal temperature. Cooking DFD PM muscle to an internal temperature 12°C higher than normal muscle produced changes associated with increasing the internal temperature of normal muscle. Similar trends, as described for the PM muscle, were observed in the QF muscle.     

The relationship between early post-mortem pH and the tenderisation of beef muscles

The rate of early post-mortem pH fall in bovine muscle was studied to determine its influence on the rate and extent of the tenderisation process. The pH of M. longissimus dorsi (LD) and M. semimembranosus (SM) muscles of Hereford cross Friesian heifers (n = 127) was taken up to 24 h post mortem. Twenty-four LD and 24 SM muscles were selected according to their rate of pH fall; slow (n = 8), intermediate (n = 8) and fast (n = 8) and were sampled at 2, 7 and 14 days post mortem for sensory, mechanical, physicochemical and biochemical analysis. Fast glycolysing LD muscles were rated more tender in sensory analysis and texture assessment whereas slow glycolysing muscles were considered significantly tougher (p < 0.001). Fast glycolysing LD had a significantly lower shear force (p < 0.001) at each stage of ageing. Slow glycolysing LD and SM had the highest shear force values. No significant difference was found in intramuscular fat or moisture content between the groups. Slow glycolysing LD muscles had shorter sarcomere lengths at 2 days post mortem. SDS-PAGE electrophoresis patterns showed increased proteolysis, such as the earlier appearance of the 30 kDa fragment, which is believed to be a good indicator of tenderness, in fast glycolysing muscle. These results suggest that the rate of post-mortem pH fall plays an important role in proteolysis and tenderisation.     

Beef longissimus lumborum, biceps femoris, and deep pectoralis Warner-Bratzler shear force is affected differently by endpoint temperature, cooking method, and USDA quality grade

Effects of endpoint temperature, cooking method, and quality grade on Warner-Bratzler shear force (WBSF) of beef longissimus lumborum (LL), biceps femoris (BF), and deep pectoralis (DP) muscles were evaluated. Eighteen of all three subprimals were selected from USDA Select and 18 from USDA Choice (Certified Angus Beef) carcasses for the respective muscles. Muscles were vacuum packaged and held at 1 °C for 14 days, frozen (-29 °C), sawed into 2.54-cm thick steaks, vacuum packaged, and stored frozen until cooking. Thawed steaks were cooked by either a Magikitch'n(?) electric belt-grill (BG) at 93 °C, or a water-bath at 93 °C, to one of nine endpoint temperatures: 40, 45, 50, 55, 60, 65, 70, 75, or 80 °C. Belt-grill cooking was much faster and resulted in distinctly less cooking loss than water-bath cooking. Water-bath cooking resulted in higher (P<0.0001) Instron(?) WBSF (31.92 N) than BG (28.25 N) for LL. The combination of Select quality grade and higher endpoint temperatures resulted in higher (P<0.05) WBSF for LL. Two distinct phases of tenderization/toughening occurred for BF. Between 40 and 60 °C, WBSF decreased from 43.95 to 38.16 N (P<0.01), whereas between 60 and 70 °C, WBSF increased from 38.16 N to 44.44 N (P<0.05). Water-bath cooling resulted in higher (P=0.0001) DP WBSF (71.12 N) than BG (59.25 N). The DP had a distinct (P<0.0001) decline in WBSF between 45 and 65 °C, irrespective of the cooking method, followed by an increase between 65 and 80 °C (P<0.01).     

Enhancing palatability traits in beef chuck muscles

Thirty-six USDA Select complexus, latissimus dorsi, rhomboideus, serratus ventralis (SEV), splenius, subscapularis, supraspinatus (SUS), and triceps brachii (TRB) muscles were studied. Muscles were assigned to one of four treatments: control, marinated, needle-pumped, and vacuum-tumbled to reach 10% brine pick-up after treatment. The solution was formulated to have 0.5% of sodium chloride and 0.4% of sodium tripolyphosphate in the end product. Steaks from the SEV, SUS, and TRB muscles were cooked on a grill and the other five muscles were oven-roasted whole, all of them cooked to an internal temperature of 71°C. Sensory evaluations and Warner-Bratzler shear force (WBSF) determinations were conducted immediately after cooking (Day-1), and after being cooked and stored frozen for 60 days (Day-60). For the Day-60 evaluation, samples were reheated using a microwave oven. The needle-pumped treatment reduced WBSF values compared to the control in 3 out of 8 muscles (P<0.05). The marinated treatment appeared to have the greatest influence on juiciness and was different from the control in 7 of 8 muscles (P<0.05). Comparing treated muscles to the control, tenderness was increased in 4 out of 8 muscles when needle pumped (P<0.05). Brine treatment reduced sensory detected connective tissue only in 2 of 8 muscles. More off-flavors were detected by the panel for marinated samples from six of eight muscles. All muscles had lower values for WBSF, less connective tissue and off-flavors, and higher juiciness, overall tenderness, and beef flavor intensity on Day-1 than Day-60. The needle-pumped method was slightly superior to the marinated and vacuum-tumbled treatments even though the differences were not always consistent. But, regardless of the application method, palatability traits were generally enhanced by brine treatments.