Physico-chemical and organoleptic properties of patties from hot, chilled and frozen goat meat

The effects of processing hot versus chilled goat meat, as such and after freezing in chunk or mince forms, were studied in relation to physico-chemical and organoleptic properties of patties. The differences in the pH of the meat samples were non-significant (P < 0·05) at 3–4 h post mortem (PM) at room temperature (30°C) and after 24 h at 4°C. The yield of the broiled patties, prepared from hot meat at 3–4 h PM, was significantly lower (P<0·05) as compared to those from chilled meat. However, this trend was reversed, if processing of hot meat into patties was done within 1–2 h PM. Freezing of chilled meat in chunk or mince forms gave significantly higher (P < 0·05) cooking yields than freezing of hot meat in similar forms.

The organoleptic scores of the raw-cooked patties were similar for all treatments. Freezing of precooked patties at −10°C for 10 days, thawing and reheating did not reduce most of the sensory scores significantly (P<0·05). Moisture, protein and fat contents of the broiled patties were not significantly (P<0·05) affected by the treatments. Standard plate count of hot versus chilled meat, for all levels of processing and storage, were within acceptable limits.     

The retail display life of steaks prepared from chill stored vacuum and carbon dioxide-packed sub-primal beef cuts

Chilled striploins and cube rolls from ten Australian steers (grain-fed for 150 days) were trimmed of external fat and cut transversely into portions approximately 10 cm thick, each weighing between 750 and 1000 g. These 'retailer-ready' cuts were each wrapped in drip saver pads and slid inside a plastic sleeve before being individually placed into a clear plastic high oxygen barrier film, metallized film or conventional vacuum bag. Cuts in clear plastic and metallized film packs were packaged in an oxygen-free saturated carbon dioxide atmosphere (CO(2)-CAP), those in vacuum bags were conventionally vacuum-packed. All packs were returned to the chiller for further cooling. After 24 hr, half the clear plastic and metallized CO(2)-CAP packs were carbon dioxide master-packed in groups of eight. Retailer-ready cuts in both clear plastic and metallized film single unit and master-packed CO(2)-CAP packs were air freighted to New Zealand and sea freighted to Japan for assessment. The control vacuum packs were all consigned to New Zealand. Assessments in both countries after 39-89 days storage at between 0 °C and -1.0 °C indicated that fat colour stability limited the retail display life of steaks cut from meat in these retailer-ready packs to approximately 48 hr. In this regard, meat from single unit CO(2)-CAP, master pack CO(2)-CAP and vacuum packs performed similarly. Lean meat colour and sensory attributes remained acceptable for up to 48 hr after displayed product was rejected because of grey-green fat discoloration. The microbiological status of retailer-ready cuts removed from CO(2)-CAP packs after 89 days chilled storage was superior to that of cuts from vacuum packs. Clear plastic and metallized film CO(2)-CAP packs performed comparably.     

The microbiology of hot and conventionally deboned vacuum packed beef

The mean numbers of aerobic bacteria were not significantly different from hot or cold, vacuum packed deboned beef, initially or on storage at 0 and 5°C. This was observed for both the psychrotrophic (4°C) and mesophilic (25°C) portions of the flora. It was possible to distinguish between the mean numbers of aerobes stored at 0 and 5°C. There were significantly higher numbers of facultative anaerobes and, in particular, lactobacilli, on hot boned cuts and for the latter organisms the psychrotrophs were predominant. For B. thermosphacta, there was no difference between cuts from hot or cold deboned beef. An accurate estimate of the psychrotrophic flora could be obtained from the mesophilic counts.     

Temperatures and ages of boxed beef packed and distributed in Canada

Boxes of beef were examined when product was packed and when boxes were loaded out of five packing plants, when boxes were loaded into and loaded out of seven refrigerated warehouses, and when boxes were received and opened at 21 retail stores. At each stage of handling at each facility, the boxes to be examined were selected at random. For each selected box, the temperature of product at the centre of the box was measured, and the date of packing and the plant of origin were noted. When cuts were packed, the minimum, median and maximum temperatures were about 2, 6 and 18 °C, respectively. Temperatures were successively lower when boxes were loaded out of packing plants, into warehouses and out of warehouses. When loaded out of warehouses, the minimum, median and maximum temperatures were about −2, 1 and 8 °C, respectively. The ranges of temperatures were similar, but the median temperatures were about 2 or 1.5 °C, respectively, when boxes were received at or were opened at retail stores. At packing plants and warehouses, the temperatures of manufacturing and ground beef were lower than those of cuts, but at the retail store the temperatures of all types of product were similar. When boxes were opened at retail stores, the minimum, median and maximum ages of cuts were about 2, 20 and 130 days, respectively; and the corresponding ages for manufacturing and ground beef were 2, 7 and 56 days, respectively. The data indicate that boxed beef is generally cooled to and maintained at temperatures within the range sought by the meat industry. However, cooling to chiller temperatures of product that is packed while warm can take several days; and some product is held for times that are excessive in view of the temperatures of boxed beef.     

Effects of hot water and lactic acid treatment of beef trimmings prior to grinding on microbial, instrumental color and sensory properties of ground beef during display

The impact of 82°C hot water (HW) or 5% lactic acid (LA) applied aerobically or by vacuum to beef trimmings prior to grinding on Salmonella Typhimurium (ATCC 1769NR; ST), Escherichia coli (ATCC 11775; EC), coliform (CO), aerobic plate count (APC), instrumental color and sensory characteristics of ground beef through simulated retail display was investigated. For this, beef trimmings were inoculated with a mixture (7 log CFU/ml each) of ST and EC, and treated either aerobically or under vacuum in a tumbler with HW or LA antimicrobials. Trimmings were ground, packaged and sampled on days 0, 1, 2, 3 and 7 of display for ST, EC, CO, APC, sensory and instrumental color characteristics. Vacuum HW or LA application had no additive effect (P>0.05) when compared with aerobic application for reducing EC, ST, CO or APC. However, lactic acid was effective for reducing (P<0.05) EC, CO and APC, but reduced ground beef redness.     

冷却肉的冷却与包装

生猪宰后胴体迅速进行冷却处理,使胴体温度在24小时内降为0～4℃,并在后续的分割、包装、流通和零售等过程中,始终处于0～4℃范围内的生鲜肉称之为冷却肉.微生物污染是冷却肉产品质量的重要危害.冷却肉的流通,目前采用加工厂内真空大包装,运输到超级市场后,制作成托盘保鲜小包装.     

Continued inhibitory effect of carbon dioxide packaging on Listeria monocytogenes and other microorganisms on normal pH beef during abusive retail display

Beef steaks of normal pH (5.3–5.5) were inoculated with Listeria monocytogenes , individually packaged in saturated carbon dioxide atmosphere packaging (SCAP) for <3 h or 5 or 8 weeks or in vacuum packaging (VP) for <3 h, and stored at −1.5°C. After each storage period, 27 individually packaged steaks were removed from their storage packs, overwrapped and placed on retail display under conditions simulating gross temperature abuse (12.25°C). Other steaks were removed from their storage packs and rinsed to remove L. monocytogenes cells, which were re-inoculated onto freshly cut beef steaks to simulate cross-contamination. These crosscontaminated steaks were overwrapped and also subjected to abusive display. Meat pH did not change significantly during storage or retail display. During the retail display of steaks previously stored in SCAP, the lag phase of aerobic bacteria and lactic acid bacteria was longer after prolonged storage compared to short (<3 h) exposure to carbon dioxide. For the same samples, L. monocytogenes failed to grow during retail display or grew only slightly after a prolonged lag phase (>75 h), even after only brief exposure time (<3 h) to carbon dioxide. In contrast, with cross-contaminated steaks, when the inocula had been exposed to SCAP or VP for a short time (<3 h) the L. monocytogenes lag phase was shorter (<20 h). Inocula from steaks stored in SCAP for 5 or 8 weeks did not grow on the cross-contaminated steaks. It is concluded that exposure of both the beef substrate and the L. monocytogenes inoculum to carbon dioxide during prolonged chilled storage does not increase the risk of growth of L. monocytogenes when that meat is subsequently placed on retail display, nor is there a large risk of growth of L. monocytogenes where cross-contamination from SCAP stored raw beef to fresh raw beef occurs prior to retail display.     

Effects of dietary vitamin e supplementation and packaging on the quality of minced beef

Friesian cattle, aged 26-27 months, were fed a diet supplemented with 2000IU α-tocopheryl acetate/kg feed/day and another group was fed a basal diet (20IU/kg feed/day) for approximately 50 days prior to slaughter. Following frozen storage (-20°C for 8 weeks) semimembranosus muscles from basal and α-tocopheryl acetate supplemented cattle were minced and vacuum packaged, aerobically packaged or packaged under modified atmospheres (MAP) (30% O(2): 70% CO(2); 70% O(2): 30% CO(2); 80% O(2): 20% CO(2)). Samples were held under refrigerated (4°C) display (fluorescent lighting, 616 lux) for eight days. Vacuum-packaged samples were held under similar conditions but in complete darkness and allowed to bloom for a minimum of 4hr prior to taking colour readings. TBARS values and Hunter a values in minced beef were measured every two days. α-Tocopherol concentrations were significantly (p<0·05) higher in minced meat samples from the supplemented group than in the basal group. Significant (p<0·05) reductions in α-tocopherol concentrations in supplemented meat samples were observed with increased concentrations of oxygen in different packaging systems after eight days of refrigerated storage. TBARS values were reduced over the whole retail display period for all packaging systems when α-tocopheryl acetate supplemented beef was used. TBARS values increased as oxygen levels increased in MAP. Hunter a values showed that vitamin E supplementation in combination with vacuum packaging and MAP improved the colour stability of meat during the first 4 days of storage, however, the failure of MAP to extend meat colour for longer periods of time was probably the result of prior storage at -20°C for 8 weeks.     

Effect of NaCl, polydextrose, and storage conditions on the functional characteristics and microbial quality of pre- and post-rigor salted beef

The functionality and microbial storage life of pre-rigor beef mince stored at −1.5 °C under vacuum or a saturated carbon dioxide atmosphere, or at −18 °C in polyethylene bags, was investigated. Salt (2% w/w) or salt plus the cryoprotectant Polydextrose^® (2%/2.6% w/w) was added pre-rigor to some samples. Chilled storage decreased salt soluble protein (SSP) by 13–18% (P < 0.01); frozen storage decreased SSP content by 20%. Pre-rigor salted mince in saturated carbon dioxide packs had a satisfactory microbial quality after 12 weeks storage. The cook yield of finely comminuted sausage batters made from that mince and from fresh pre-rigor mince were similar, although batter stress and strain decreased with chilled storage. Adding Polydextrose^® to salted mince improved batter strain compared with the non-additive and salt-only samples and improved batter stress compared with the salt-only samples. The microbial storage life of chilled vacuumpacked unsalted mince was less than 6 weeks; pre-rigor salting increased its storage life.     

Colour stability of bovine Longissimus and Psoas major muscle as affected by electrical stimulation and hot boning

From eight electrically stimulated and eight non-stimulated cows the righthand-side longissimus and psoas major muscles were hot boned within 1 1 2 h post mortem, vacuum packaged and chilled and storred at 1±1°C. Immediately after slaughter, the lefthand carcass-sides were blast-chilled for 1 1 2 h and subsequently chilled at 1±1°C until the following day. After cold boning, the longissimus and psoas major muscle were packaged, chilled and stored as the hot boned muscles. After 12 days of storage, steaks, cut from the primals, were displayed at 1±1°C under continuous illumination (300-400 lx). Colour measurements after 0, 2 and 4 days of display revealed a significant (p<0·10) effect of time of boning on non-stimulated psoas major muscle (lower values for a (?), b (?) values, chroma and %R630-%R580). Significant effects of electrical stimulation were not observed. Changes in hue tended to be more pronounced when the meat had been stimulated. Changes in chroma were largest (p<0·10) is non-stimulated, hot boned psoas muscle. Analysis of variances showed that in the longissimus muscle significant effects (p<0·10) of time boning and electrical stimulation were present. The effect of time of boning was often influenced by the use of electrical stimulation. Changes in hue and chroma indicated that hot boned samples had a higher colour stability than cold boned controls, especially when the carcasses had not been stimulated electrically. The observed differences in colour stability were rather small in all treatment groups and are not expected to present any practical merchandising problem.     

Calpains from thaw rigor muscle

Pre-rigor beef M. Longissimus lumborum and diaphragma were frozen at −70 °C and thawed at different temperatures and the activities of extracted calpains and the toughness of heated meat compared with those in chilled muscle.

Fresh muscle contained about 14 μg of μ-calpain/g and was unaffected by freezing, but was reduced after thawing. Rapid thawing at 30 °C for 20 min reduced the μ-calpain to 14%. When cooked from the frozen state, extensive shortening occurred and tender meat was obtained.

By storing at −3 °C for 1 day, thaw-shortening was prevented, but tougher meat obtained. The μ-calpain decreased to 70% whilst the m-calpain was unaffected. Toughness decreased after further storage at −3 °C, as did the μ-calpain. The latter changes were similar to those during development of rigor mortis and ageing of non-shortened meat stored at 4 °C. Variation in calpain activity, rather than in sarcomere length, are likely to be the cause of toughness variation in thaw rigor muscle.     

Fatty acid content and composition of english beef, lamb and pork at retail

We have determined the fatty acid content and composition of retail samples of meat and assessed them with respect to UK dietary recommendations. Fifty beef sirloin steaks, pork chops and lamb chops were purchased from four supermarkets on separate occasions. The percentage of muscle (boneless basis) in the samples was 84.4 ± 4.3, 69.8 ± 7.7 and 78.9 ± 7.1 for beef, lamb and pork, respectively, with fatty acid contents of 3.84 ± 1.3, 4.73 ± 1.66 and 2.26 ± 0.7 g per 100 g muscle, respectively. Adipose tissue fatty acid contents were 70.0 ± 8.2, 70.6 ± 8.6 and 65.3 ± 9.4 g per 100 g tissue. A range of C20 and C22 polyunsaturated fatty acids (PUFA) was present in the muscle of all three species and pork adipose tissue but their concentrations in lamb and beef adipose tissue were too low to measure. The mean P:S ratios for beef, lamb and pork muscle were (adipose tissue values in parentheses): 0.11 (0.05); 0.15 (0.09) and 0.58 (0.61), and the n−6:n−3 ratios were 2.1 (2.3), 1.3 (1.4) and 7.2 (7.6). We conclude that the muscles of red meat species are a valuable source of PUFA, particularly the C20 and C22 n−3 fatty acids, in the human diet and that, considered as part of a varied diet, the low P:S ratio of the ruminant muscle, the high n−6:n−3 ratio of pork and the total fatty acid contents do not detract significantly from the nutritional value of lean meat.     

Survival of Campylobacter jejuni on beef and pork under vacuum packaged and retail storage conditions: examination of the role of natural meat microflora on C. jejuni survival

The ability of Campylobacter jejuni ATCC 11168 to survive on beef and pork stored under chilled, vacuum packaged and retail display conditions were examined. In addition, the effect of natural microflora on commercial beef and pork on the survival of C. jejuni under these storage conditions was examined. When sterile cores of beef and pork were inoculated with ∼10⁵ to 10⁶ cfu cm⁻²C. jejuni, and were stored under aerobic or vacuum packaged conditions at −1.5 or 4 °C, its numbers dropped significantly and C. jejuni could not be enumerated by direct plating after 21 d of the 6 wks study. In contrast, survival of C. jejuni on commercial vacuum packaged beef and pork was significantly enhanced, resulting in only 1 log cfu cm⁻² reduction at the end of 6 wks. During 7 d of display in a retail case, numbers of C. jejuni dropped quickly, but could be enumerated by direct plating even after the 7 d. The presence of high numbers of inoculated C. jejuni on beef and pork had no significant effect on the natural microflora numbers compared to uninoculated controls when the meat was stored either in vacuum or in a retail display case. These results show that natural microflora on vacuum packaged meat afford enhanced survival of C. jejuni present on the surfaces of both beef and pork when stored at refrigeration temperatures. Hence, strict hygienic practices or the implementation of decontamination technologies are recommended to ensure safety of meat with respect to this pathogen.     

Effects of Beef Carcass Electrical Stimulation and Hot Boning on Display Color of Unfrozen Vacuum Packaged Steaks

Ninety-six beef sides from 48 carcasses were used to determine effects of control (C, chilled 48 hr at 5°C), electrical stimulation (ES, 45 min postmortem, 400 volts for 2 min, pulsed), and hot boning (HB, 2 hr postmortem), and combination (ESHB) treatments on muscle color of longissimus (LD) and semimembranosus (SM), vacuum packaged steaks. HB muscles frequently were visually brighter purplish-red than other treatments. Compared to ESHB, ES LD was not different, but ES SM was duller purplish-red in color. Reflectance indicators of reduced myoglobin and metmyoglobin were essentially the same across treatments in both muscles. Vacuum packaged fresh beef steaks from all treatments were acceptable in color at 0, 3, 7, and 14 days of display. Vacuum packaging appears suitable for steaks from any of these carcass treatments but is especially useful for steaks from hot boned cuts.     

Effect of freezing on sensory quality, shear force and water loss in beef M. longissimus dorsi

The objective of this study was to determine how sensory quality, shear force and water loss differ between beef stored either chilled or frozen before cooking. Meat tenderness was analysed instrumentally and sensorially using both a consumer panel and a semi-trained panel. Both M. longissimus dorsi (LD) from eight young Holstein bulls were cut into eight samples, weighed, vacuum packed and aged at 4 °C for 2, 7 or 14 days. After ageing, the frozen samples were kept at −20 °C prior to heat treatment. Water holding capacity was recorded as purge or thawing loss and cooking loss or as combined loss. Sensory analyses were performed on samples aged 7 days. Peak force values declined with ageing time and freezing. Frozen meat aged 2 days had the same peak force values as chilled meat aged 7 days. Total energy was the same for both treatments at day 2 and 7, whereas at day 14 frozen samples showed significantly higher values than chilled samples. The sensory panel experienced the chilled meat to be more tender, juicier and having a more intense meat taste than the frozen meat, whereas the consumers could not find any significant difference in degree of liking. Water holding capacity was lower for the frozen samples. The results indicate that conclusions from studies concerning sensory quality of beef will depend on whether the meat has been kept chilled or frozen before testing.     

Effects of Chilling Method on the Sensory, Chemical and Cooking Characteristics of Ground Beef Patties

Hot-boned beef (excised 90 min postmortem) was chilled either by mixing coarse ground beef with CO₂ snow or by immersing ground beef chub packs in a brine chiller (-2°C). Hamburger patties were prepared from both hot and cold-boned chub packed, coarse ground beef after 0, 7, 14, and 21 days of storage (0°C). Microbiological quality of the hot-boned ground beef was either superior or equal to that of the control. Purge present in all the chub packs after 21 days of storage was 1.0%. Patties prepared from CO₂ chilled ground beef were more tender than control patties. Patties prepared from brine-chilled ground beef had greater cooking losses than patties prepared from cold-boned ground beef.     

Influence of packaging method and length of chilled storage on microflora, tenderness and colour stability of venison loins

Sections of venison loins (LD) weighing approximately 300 g from 12 red deer (Cervus elaphus) were packaged using four packaging methods: (a) vacuum packaging, (b) CO₂ flushed using a nylon containment film (CO₂-Nylon), (c) CO₂ flushed using an ultra-high barrier containment film (CO₂-UHB), and (d) CO₂ flushed using an aluminium foil laminate containment film (CO₂-Foil) and stored for 1, 6, 12 and 18 weeks at 0°C. Meat pH values were lower in all CO₂ flushed meat packages (P<0·05) than in vacuum packaged meat. Lactic acid bacteria and total anaerobic counts increased over storage time in all packages regardless of treatment up to values of log₁₀ 7·8 and 7·6 g⁻¹, respectively. Tenderness tended to increase as meat was stored for up to 18 weeks. Colour scores taken during simulated retail display indicated that colour deteriorated more rapidly when meat was stored for 12 and 18 weeks than for 1 and 6 weeks. Vacuum packaging and gas flushing (CO₂-Foil) resulted in higher initial colour scores than venison packaged in the CO₂-Nylon or CO₂-UHB materials. Venison stored for 18 weeks also exhibited a higher proportion of packages containing off odours, lower flavour desirability and flavour intensity scores as well as higher off flavour scores than meat stored for shorter times. The implications of these effects are discussed. Although there were few significant differences in microbial growth and sensory characteristics due to packaging method or containment film, vacuum packaging appeared to be the most economic and produced meat of better colour stability.     

The effect of post-mortem ageing and heating on water retention in bovine muscles

The muscles semitendinosus (ST) and psoas major (PM) were removed from chilled young bull carcasses 24 h after slaughter and stored at 4 °C. At the 1st, 6th and 12th day of post-mortem ageing the chemical composition (moisture, fat, protein, collagen) and contents of free, immobilized and unfreezable water in the muscles were estimated. The muscle steaks were boiled at 100 °C, roasted at 170 °C or fried at 160 °C to an internal temperature of 75 °C, and the amounts of total, free, immobilized, and unfreezable water in heated muscles were evaluated. The unfreezable water was estimated by DSC. In the raw muscles immobilized water constituted 74–75%, free water 16.6–17.6% and unfreezable water 7–8% of the total water. Independent of time of ageing, PM muscle contained significantly more free water than ST muscle. During post-mortem ageing, changes in free, immobilized and unfreezable water in muscles were not significant. The level of free water was highest in boiled and least in fried meat, however the amount of immobilized water was highest in fried and lowest in boiled meat. The amount of unfreezable water in muscles heated after 12 days of post-mortem ageing decreased.     

去骨方法对牛肉和火鸡肉化学成分及一些特性的影响

本文针对机械去骨和人工去骨的牛肉以及火鸡肉的一些化学、物理特性进行了对比研究。相近成分胆固醇、硫代巴比土酸(TBA)、钙铁含量、颜色参数、脂肪酸成分等指标在样本中得以分析。去骨方法对牛肉和火鸡肉的化学成分有所影响。机械去骨导致较高的胆固醇以及钙铁含量。在手工去骨火鸡肉中,含量最多的脂肪酸是C16:0、C18:1以及C18:2。机械去骨加工使火鸡肉中C18:1、C18:2、C18:3的含量增加。而C16:0、C18:0、C18:1则是机械去骨和手工去骨牛肉中主要的脂肪酸。     

The colour and colour stability of beef Longissimus dorsi and Semimembranosus muscles after effective electrical stimulation

The influence of effective low voltage electrical stimulation (ES) of beef on the colour and colour stability of longissimus dorsi (LD) and semimembranosus (SM) muscles, during storage and retail display was studied by tristimulus colorimetry and reflectance spectrophotometry. ES had no significant effect on the colour of the LD muscles, but some significant effects on SM muscles of ultimate pH 5·5-5·7. Three hours after slicing into steaks at 5 days post mortem, stimulated SM muscles had a paler/lighter colour than non-stimulated controls. During a retail display of 3 days, all steaks exhibited a loss of colour quality manifested in loss of redness and decreases in both hue and chroma (saturation). These changes were most marked in the stimulated SM muscles, and analysis indicated that they were due almost exclusively to the formation of metmyoglobin (metMb). Ageing the meat, as primals cuts, for 33 days at 0°C led to no significant differences in the perceived colour three hours after slicing. The colour changes observed during the 3-day retail display of steaks occurred more rapidly in both (ES and non-ES) 33 day-aged samples than in the 5 day-aged ones. The result of this was that the colour stability of non-stimulated steaks prepared at 33 days was similar to that of ES steaks prepared fresh (5 day post mortem). In SM muscles of pH 5·8-6·0 the apparent differences in colour of the ES and non-ES samples were not significant. However, meat of pH > 5·8, although darker than meat of lesser pH, had less tendency to form metmyoglobin during retail display.

The present work also confirmed that seemingly small differences in display conditions, especially temperature, have a marked effect on metmyoglobin formation.