Effect of selected modified atmosphere packaging on Campylobacter survival in raw poultry.

Most current research on Campylobacter has focused on preharvest or processing plant cross-contamination. Little is known about the effect of storage environment on the survival of Campylobacter on raw poultry. We evaluated the effects of modified storage atmosphere and freezing on the survival of naturally occurring Campylobacter on raw poultry. Broiler carcasses (n = 560) were collected as they exited the chiller in 2 commercial processing plants and were sampled for the detection of Campylobacter, Escherichia coli, psychrophiles, and total aerobes at 0 and 14 d of refrigerated (2°C) storage. Gases evaluated were air, 100% O(2), 100% CO(2), and a standard poultry modified atmosphere packaging mixture (5% O(2) + 10% CO(2) + 85% N). Freezing was included as a control group. All carcasses were sampled by the whole-carcass rinse method. The rinse fluid was recovered and pooled from 5 individual rinses, and serial dilutions were made for examination of Campylobacter (42°C, 48 h), E. coli (37°C, 24 h), psychrophiles (plate count agar, 4°C, 7 d), and total aerobic bacterial populations (plate count agar, 37°C, 24 h). Campylobacter counts for all treatments were reduced during the 14-d storage period but the 100% O(2) treatment caused a significantly (P < 0.05) greater reduction than the other gas treatments. For the psychrophiles, storage in air resulted in the greatest growth after 14 d, with reduced psychrophilic growth allowed by either O(2) or the modified atmosphere packaging mixture (not different from each other). Of the treatments evaluated, CO(2) allowed the least growth of psychrophiles. Proliferation of E. coli and aerobes was the greatest when packaged in air after 14 d, whereas CO(2) packaging resulted in the least growth. These data suggest that storage under O(2) may reduce Campylobacter recovery and slow psychrophile and aerobe recovery following storage.

Lipid oxidation stability of omega-3- and conjugated linoleic acid-enriched sous vide chicken meat.

Lipid oxidation is known to occur rather rapidly in cooked chicken meat containing relatively high amounts of polyunsaturated fatty acids. To assess the lipid oxidation stability of sous vide chicken meat enriched with n-3 and conjugated linoleic acid (CLA) fatty acids, 624 Cobb × Ross broilers were raised during a 6-wk feeding period. The birds were fed diets containing CLA (50% cis-9, trans-11 and 50% trans-10, cis-12 isomers), flaxseed oil (FSO), or menhaden fish oil (MFO), each supplemented with 42 or 200 mg/kg of vitamin E (dl-α-tocopheryl acetate). Breast or thigh meat was vacuum-packed, cooked (74°C), cooled in ice water, and stored at 4.4°C for 0, 5, 10, 15, and 30 d. The lipid oxidation development of the meat was estimated by quantification of malonaldehyde (MDA) values, using the 2-thiobarbituric acid reactive substances analysis. Fatty acid, nonheme iron, moisture, and fat analyses were performed as well. Results showed that dietary CLA induced deposition of cis-9, trans-11 and trans-10, cis-12 CLA isomers, increased the proportion of saturated fatty acids, and decreased the proportions of monounsaturated and polyunsaturated fatty acids. Flaxseed oil induced higher deposition of C18:1, C18:2, C18:3, and C20:4 fatty acids, whereas MFO induced higher deposition of n-3 fatty acids, eicosapentaenoic acid (C20:5), and docosahexaenoic acid (C22:6; P < 0.05). Meat lipid oxidation stability was affected by the interaction of either dietary oil or vitamin E with storage day. Lower (P < 0.05) MDA values were found in the CLA treatment than in the MFO and FSO treatments. Lower (P < 0.05) MDA values were detected in meat samples from the 200 mg/kg of vitamin E than in meat samples from the 42 mg/kg of vitamin E. Nonheme iron values did not affect (P > 0.05) lipid oxidation development. In conclusion, dietary CLA, FSO, and MFO influenced the fatty acid composition of chicken muscle and the lipid oxidation stability of meat over the storage time. Supranutritional supplementation of vitamin E enhanced the lipid oxidation stability of sous vide chicken meat.

Dietary lipid source and vitamin E effect on lipid oxidation stability of refrigerated fresh and cooked chicken meat.

The fatty acid composition of chicken muscle may affect the lipid oxidation stability of the meat, particularly when subjecting the meat to thermal processing and storage. The objective of this study was to evaluate the diet effect on lipid oxidation stability of fresh and cooked chicken meat. Six hundred broilers were raised for a 6-wk feeding period and were assigned to 8 treatments with 3 repetitions. Broilers were fed a basal corn-soybean meal diet, including 5% of either animal-vegetable, lard, palm kernel, or soybean (SB) oil, each supplemented with a low (33 mg/kg) or high (200 to 400 mg/kg) level of vitamin E. Fresh breast and thigh meat and skin were packaged and refrigerated (4°C) for 15 d. Breast and thigh meat were frozen (-20°C) and stored for ~6 mo and then thawed, deboned, ground, and formed into patties of 150 g each. Patties were cooked (74°C), cooled, packaged, and stored in refrigeration for 6 d. The lipid oxidation development of the products was determined using the TBA reactive substances analysis. The results showed that the lipid oxidation development, in both fresh chicken parts and cooked meat patties, was influenced by the interaction of either dietary lipid source or vitamin E level with storage time. Fresh breast meat showed no susceptibility to lipid oxidation, but thigh meat and skin presented higher (P < 0.05) malonaldehyde values in the SB oil treatment, starting at d 10 of storage. In cooked patties, during the entire storage time, the SB oil showed the highest (P < 0.05) lipid oxidation development compared with the other treatments. Regarding vitamin E, in both fresh parts and cooked meat patties, in most sampling days the high supplemented level showed lower (P < 0.05) malonaldehyde values than the control treatment. In conclusion, the lipid oxidation stability of chicken meat is influenced by the lipid source and vitamin E level included in the diet upon storage time and processing of the meat.

Soybean, palm kernel, and animal-vegetable oils and vitamin E supplementation effect on lipid oxidation stability of sous vide chicken meat.

There is an increasing demand in precooked chicken meat products for restaurants and catering services. Because cooked chicken meat develops lipid oxidation relatively fast, sous vide chicken meat was studied to assess its shelf-life. Six hundred Cobb x Ross broilers were fed for 6 wk with a basal corn-soybean meal diet including soybean, palm kernel, or animal-vegetable oil, each supplemented with 33 or 200 mg/kg of dl-alpha-tocopheryl acetate. Broilers were randomly assigned into 6 treatments and 4 repetitions with 25 birds each. Boneless breast or thigh muscle pieces were dissected into 5 x 5 x 5 cm cubes, vacuum-packed, cooked in water bath (until 74 degrees C internal temperature), chilled, and stored at 4 degrees C for 1, 5, 10, 25, and 40 d. For each storage day, each pouch contained 3 pieces of meat, either breast or thigh. Thiobarbituric acid reactive substances analysis, to quantify malonaldehyde (MDA) values, was conducted to estimate the lipid oxidation development. Nonheme iron values of cooked meat were analyzed. Fatty acid methyl esters analysis was performed in chicken muscle to determine its fatty acid composition. There was no interaction between dietary fat and vitamin E level in all of the variables studied except in nonheme iron. Dietary fat significantly influenced the fatty acid composition of the muscle (P < 0.01), but it did not affect the MDA values, regardless of differences in the muscle fatty acid composition between treatments. Supplementation of the high level of vitamin E significantly reduced the MDA values in both breast and thigh meat (P < 0.01). The maximum MDA values were observed at d 40 of storage in thigh and breast meat in animal-vegetable and soybean oil treatments with the low levels of vitamin E, 0.91 and 0.70 mg/kg, respectively. Nonheme iron values in thigh meat differed between treatments at 1 or 25 d of storage but not in breast meat. In conclusion, refrigerated sous vide chicken meat has a prolonged shelf-life, which is enhanced by dietary supranutritional supplementation of vitamin E.

Research developments in pale, soft, and exudative turkey meat in North America.

Pale, soft, and exudative (PSE) refers to meat that is pale in color, forms soft gels, and has poor water-holding ability. Most frequently used in reference to pork, this defective meat is being seen with increasing frequency in turkey and broiler processing plants. It has been estimated that this PSE-type meat represents 5 to 40% of meat that is produced in the poultry industry. With the increased production of further-processed products, this PSE problem has become more apparent in the turkey industry. It has been estimated that due to the high incidence, a single turkey processing plant could be losing $2 to 4 million per year, resulting in a loss in excess of $200 million dollars by the turkey industry alone.

Factors influencing the variation in tenderness of seven major beef muscles from three Angus and Brahman breed crosses.

Beef carcasses (n=30) from 3/4 Angus (A)×1/4 Brahman (B), 1/4A×3/4B, and 1/2A×1/2B F(1) crosses were used to evaluate breed type, electrical stimulation, and postmortem aging on the M. semimembranosus (SM), M. semitendinosus (ST), M. biceps femoris (BF), M. vastus lateralis (VL), M. gluteus medius (GM), M. longissimus dorsi lumborum (LD), and M. triceps brachii (TB). Shear force values decreased with increased postmortem aging to a greater extent in steaks from 3/4A×1/4B than steaks from the other breed types. Shear force values for steaks from the round (SM, ST, BF, VL) were higher than steaks from the loin (LD, GM) and chuck (TB) for both electrically stimulated and non-electrically stimulated muscles. In the LD muscle, calpastatin activities were similar among breed types. Muscle type played the greatest role in determining tenderness.

Comparison of flavor changes in cooked-refrigerated beef, pork and chicken meat patties.

Beef and pork longissimus dorsi (LD) and semimembranosus (SM) and chicken breast (B) and thigh (T) muscles excised 24 h postmortem were ground by muscle/species group, formed into patties, pan-fried, refrigerated for 0, 3 or 6 days, and evaluated by a trained sensory panel for intensity of specific flavors. The rate of decline in species-specific natural meat flavor intensity and the rate of increase in "cardboard" (CBD) flavor intensity during the first half of the 6-day storage were fastest for beef, while such decline and increase during the entire storage period were slowest for chicken B. Overall trends of natural meat flavor and CBD intensity changes for chicken T appeared more like those for the red meats than chicken B. It was concluded that, while flavor deterioration can occur in cooked-stored meats from all the species, quantitative or the magnitude of differences between species would depend on muscle types and sensory terms/method used.

Early postmortem carcass trim effects on the tenderness of broiler breast fillets.

Broiler carcasses are often trimmed during evisceration to remove damaged areas of the carcass. Because deboning before rigor mortis development can toughen meat, trimming during evisceration may toughen the meat. This study evaluated the effects of trimming on the tenderness of broiler breast meat. To evaluate the effect of wing removal on tenderness, breast halves from 2 flocks were collected after chilling at a commercial plant. One-third were untrimmed controls, one-third had small amounts of breast meat removed with wing (WMin), and one-third had large amounts of breast meat removed with wing (Wmax). Salvage fillets from the 2 flocks were also collected from the salvage table of the plant. Carcasses were also processed to evaluate the effect of breast blister trimming that removed a superficial amount of muscle tissue, half of which had breast blister trims, and half did not. All front halves or carcasses were aged until 24 h postmortem and deboned. Salvage fillets were held refrigerated until 24 h postmortem. Fillets were cooked and then sheared in 2 locations on the fillet, upper and lower, to determine if tenderness was more affected at areas close to the trim. Carcasses with wing trims had significantly higher shear values compared with the control, and shear values from the upper portion of the fillets from the WMax and WMin (nearer the trim) were significantly greater than for the lower portion. Location, however, did not affect shear values in the control carcasses. This finding indicated that tenderness of the areas nearest the trim might be affected more by the trim process. Salvage table deboning significantly increased shear values throughout the fillet. There was no significant difference in shear value due to breast blister trimming. The results of this study suggest that trimming carcasses by wing or breast fillet removal results in decreased meat tenderness.

Research note: Functionality of electrically stimulated broiler breast meat.

Postmortem electrical stimulation (ES) tenderizes meat by acceleration of adenosine triphosphate (ATP) depletion, pH decline, and physical disruption of muscle fibers. It has been demonstrated that rigor development at elevated temperatures, as with slow chilling, can cause meat to develop pale color and poor water-holding capacity. The objective of this study was to compare the functionality of broiler breast meat from control and electrically stimulated carcasses with and without normal rapid chilling. Broilers were either electrically stimulated (450 mA, 450 V, 2 s on, 2 s off for 7 pulses) immediately after bleeding or used as nonstimulated controls. The ES birds were either chilled immediately (ES2) or had chilling delayed for 2 h at room temperature (ESD2). All ES breast fillets were harvested at 2 h postmortem. The control carcasses were chilled immediately and had fillets harvested at 2 h postmortem (C2) or at 8 h postmortem (C8). Electrical stimulation accelerated pH decline and prevented toughening when breast meat was deboned at 2 h postmortem, regardless of chilling rate. The water released from the gels during cooking was higher for the ESD2 than the ES2 group, which was not different from the C2 group, suggesting that ES followed by slow chilling reduced water-holding capacity compared with the ES2 and C2 groups. There were no differences in expressible moisture, gel strength, or lightness among the ES2, ESD2, and C2 treatments. These results indicated that high voltage ES followed by normal chilling did not impair protein functionality or cause pale, soft, exudative meat. However, there was some evidence that slow chilling after ES may negatively affect some water-holding properties of the meat.

Skin pigmentation evaluation in broilers fed natural and synthetic pigments.

Broiler carcass skin color is important in the United States and Mexico. This study evaluated the use of natural and synthetic pigments in broiler diets at commercial levels. Birds were fed natural or synthetic pigments at low or high levels, simulating US and Mexican commercial practices. Skin color was measured during live production (3 to 7 wk of age) and after slaughter and chilling. The natural pigments had consistently greater skin b* values (yellowness) than the synthetic pigments. The high levels produced greater skin b* values than the low levels, regardless of source. The synthetic pigments had a slower increase in skin b* but reached the same level as the natural low by 7 wk. There was no difference in skin a* values (redness) due to pigment source or level or the age of the bird. By 7 wk, all pigment sources approached plateau levels in the blood, but the synthetic pigment diet produced higher blood levels of yellow and red pigments than the natural pigment diets. Processing intensified skin yellowness and reduced skin redness. These data suggest that although synthetic pigments might have been absorbed better than natural ones, natural pigments were more efficient at increasing skin yellowness and there were only small differences between high and low levels for each pigment source. This finding may allow reduction in pigment use and feed cost to achieve the same skin acceptance by the consumer.

Tenderizing spent fowl meat with calcium chloride. 1. Effects of delivery method and tumbling.

In this study, different methods of 0.2 M or 0.3 M CaCl2 delivery into hot-boned spent Leghorn breast fillets followed by tumbling were evaluated. The CaCl2 was delivered by adding 10% (wt/wt) solution into the tumbler, injection 10% (wt/wt) into the fillet, or soaking at room temperature for 15 min followed by soaking at 2 C for 45 min. All these treatments were subjected to either tumbling at room temperature for 1 h or no tumbling. Water injected and untreated samples served as controls. All fillets were baked and sheared with an Allo-Kramer cell. Introduction of 0.2 M CaCl2 through different delivery methods was not sufficient to improve spent fowl meat tenderness, even when followed by tumbling. When 0.3 M CaCl2 injection was followed by tumbling, the mean shear value of the hot-boned spent hen fillets was reduced to near the tenderness level acceptable to consumers. However, when tumbling was performed on the fillets treated with calcium introduced by methods other than injection, the shear values were higher than samples using the calcium injection method. Therefore, tumbling in combination with injection of 0.3 M CaCl2 is essential for maximal tenderization of spent fowl meat.

Tenderizing spent fowl meat with calcium chloride. 3. Biochemical characteristics of tenderized breast meat.

Biochemical characteristics of spent fowl meat injected with calcium chloride or sodium chloride were evaluated. Hot-boned breast fillets were injected to 10% (wt/wt) with 0.3 M CaCl2 or 0.6 M NaCl, tumbled, and aged 24 h. Tumbling was conducted at 20 C, -635 mm Hg, 20 rpm for 1 h. Hot-boned and cold-boned (24 h) fillets were used as controls. One fillet from each carcass was baked and sheared with an Allo-Kramer cell, whereas the other fillet was used for biochemical analysis. Shear values indicated that both CaCl2- and NaCl-treated samples had significantly (P < 0.05) lower shear values than hot-boned controls but were similar (P > 0.05) to cold-boned samples. The CaCl2 injection treatment significantly elevated (P < 0.05) the tissue calcium content compared to all other treatments. There was no significant difference in heat-stable collagen content (P > 0.05) among all treatments, which indicated that CaCl2 or NaCl did not contribute to meat tenderness through degradative changes in collagen. Calpain data indicated that mu-calpain had disappeared by 24 h aging in all treatments. The m-calpain activity was significantly lower (P < 0.05) in samples treated with CaCl2 than in the other samples. The NaCl-treated samples had m-calpain activity similar (P > 0.05) to that of hot-boned controls. Sarcomeres of CaCl2-treated samples were significantly shorter (P < 0.05) than those of cold-boned controls, were similar (P > 0.05) to those of hot-boned controls, and were shorter than those of NaCl-treated muscles. The sarcomere length and calpain data suggest that CaCl2 tenderized fillets by ionic strength and calcium-specific effects (possibly a proteolytic action), whereas the NaCl solution tenderized by ionic strength effect at a similar conductivity level to that of the CaCl2 solution.

Meat quality during processing.

The study of growth and development of any food animal such as poultry needs to consider the effects of the muscle changes on the use of the muscle as meat. If a treatment could increase muscle growth but the increased meat was of poor quality, then the increase in production would be of little value. Muscle is of particular concern because not only is it the tissue of greatest value for food, but it also is an excitable tissue and responsive to its environment. Many of these responses can be quite deleterious to meat quality. The basis for the response of muscle to its environment is in postmortem metabolism and the simultaneous development of rigor mortis. Although the animal may die in a matter of minutes following the neck cut, its muscle cells continue to metabolize and respond for hours after respiratory cessation and brain death. During these hours, the muscle has energy that fuels the responses to the environment, most commonly in terms of color and texture. Heat, transportation, and handling all contribute to the preslaughter stress that can alter color, texture, and related protein functionality. Stunning is another preslaughter factor that has a large effect on postmortem metabolism and meat quality. After death, chilling can toughen meat while it adds juiciness, and aging prevents the meat from toughening in response to deboning. Electrical stimulation is a recent beneficial innovation that reduces the need for aging by accelerating postmortem energy depletion and reducing the muscle's ability to toughen during deboning. This paper reviews the responsiveness of the muscle and gives examples of how these responses can hurt or help meat quality.

Fragmentation, tenderness, and post-mortem metabolism of early-harvested broiler breast fillets from carcasses treated with electrical stimulation and muscle tensioning.

Two 72-bird trials were conducted to determine the effects of 15 s electrical stimulation (ES) (440 V, 2 s on and 1 s off) and prechill muscle tensioning (MT) on fragmentation, tenderness, and post-mortem metabolism of early-harvested (1 h post-mortem) broiler breast fillets. Compared with controls, all treatments increased sarcomere length and decreased shear value. Electrical stimulation reduced muscle pH values. Histological examination of samples from fillets harvested early and then aged 24 h revealed that all treatments increased fiber disruption compared with controls. Both fragmentation and excessive sarcomere shortening prevention were important to the improvement in fillet tenderness associated with the ES and MT treatments.

Evaluation of physical dimension changes as nondestructive measurements for monitoring rigor mortis development in broiler muscles.

Studies were conducted to develop a non-destructive method for monitoring the rate of rigor mortis development in poultry and to evaluate the effectiveness of electrical stimulation (ES). In the first study, 36 male broilers in each of two trials were processed at 7 wk of age. After being bled, half of the birds received electrical stimulation (400 to 450 V, 400 to 450 mA, for seven pulses of 2 s on and 1 s off), and the other half were designated as controls. At 0.25 and 1.5 h postmortem (PM), carcasses were evaluated for the angles of the shoulder, elbow, and wing tip and the distance between the elbows. Breast fillets were harvested at 1.5 h PM (after chilling) from all carcasses. Fillet samples were excised and frozen for later measurement of pH and R-value, and the remainder of each fillet was held on ice until 24 h postmortem. Shear value and pH means were significantly lower, but R-value means were higher (P < 0.05) for the ES fillets compared to the controls, suggesting acceleration of rigor mortis by ES. The physical dimensions of the shoulder and elbow changed (P < 0.05) during rigor mortis development and with ES. These results indicate that physical measurements of the wings maybe useful as a nondestructive indicator of rigor development and for monitoring the effectiveness of ES. In the second study, 60 male broilers in each of two trials were processed at 7 wk of age. At 0.25, 1.5, 3.0, and 6.0 h PM, carcasses were evaluated for the distance between the elbows. At each time point, breast fillets were harvested from each carcass. Fillet samples were excised and frozen for later measurement of pH and sacromere length, whereas the remainder of each fillet was held on ice until 24 h PM. Shear value and pH means (P < 0.05) decreased, whereas sarcomere length means (P < 0.05) increased over time, indicating rigor mortis development. Elbow distance decreased (P < 0.05) with rigor development and was correlated (P < 0.01) with shear value (r = 0.2581), sarcomere length (r = -0.3079), and pH (r = 0.6303). These results suggest that elbow distance could be used in conjunction with other detection methods for optically automating measurement of rigor mortis development in broiler carcasses.

The role of carcass chilling rate in the development of pale, exudative turkey pectoralis.

Pale, soft, and exudative meat is a growing problem in the turkey industry that has been associated with processing conditions such as improper chilling. This condition is caused by accelerated postmortem glycolysis while carcass temperatures are still elevated, resulting in protein denaturation and poor meat quality. To evaluate the involvement of chilling rate, 48 toms were conventionally processed at 17.5 wk of age and chilled at 0,10, 20, or 30 C for 45 or 90 min and deboned. Temperature and pH of the breast fillet were recorded at 15 min, deboning time, and at 24 h postmortem (PM). Drip loss, L* value, expressible moisture, gel strength, and cook loss were determined on the fillets at 24 h PM. At 15 min PM, there were no temperature differences among treatments. At deboning, the carcasses chilled at 30 C had the highest fillet temperature and had significantly lower pH values when compared to those chilled at 0 and 10 C. L* value was significantly higher in carcasses chilled at 30 C and deboned at 60 min PM when compared to 0 and 10 C chilled carcasses. There were no significant differences in L* values at 105 min and 24 h PM among any treatment group. Drip loss and cook loss were significantly higher in carcasses chilled at 30 C compared to the remaining treatments. There were no differences in expressible moisture at 60 or 105 min PM or gel strength at 60 min PM in any of the treatments. However, at 105 min PM, carcasses chiled at 0 C had higher gel strength when compared to the remaining treatments. These results indicate that there is a relationship between chilling rates and meat quality with slower chilling producing PSE-like characteristics.

A comparison of texture and quality of breast fillets from broilers stunned by electricity and carbon dioxide on a shackle line or killed with carbon dioxide.

To compare the broiler breast muscle quality resulting from three different slaughter methods, 36 broilers in each of two replicates were randomly divided into three groups receiving CO2 stunning, electrical stunning (ES), or CO2 killing. Carbon dioxide stunning was accomplished in a tunnel with a gradient from 40 to 60% CO2 by allowing the broilers on shackles to pass through the tunnel for 25 s. Electrical stunning was done by passing the bird's head through a charged 1% brine solution (35 mA, 7 s). For CO2 killing, the birds were killed by asphyxiation in an atmosphere of less than 2% oxygen (air displaced by CO2) for 2.5 min. Following slaughter, all breast fillets were harvested at 1.25 h postmortem and analyzed for pH, R value, shear value (SV), expressible moisture, and color (lightness and redness at 1.25 and 24 h postmortem). There were no differences (P<0.05) between treatments in pH, R value, SV, 1.25-h color values, or expressible moisture. There was an increase (P<0.05) in lightness between 1.25 and 24 h postmortem in all treatments, with the CO2 stun exhibiting the greatest increase and resulting in a significantly greater L* value at 24 h postmortem than the CO2 killing treatment. These results suggest that the postmortem metabolism or characteristics of the meat from animals processed with these stunning or killing methods does not differ to a large extent.

Muscle metabolism and meat quality of Pectoralis from turkeys treated with postmortem electrical stimulation.

This experiment was conducted to evaluate the effects of electrical stimulation (ES) on muscle metabolism and breast meat quality in turkeys. Thirty-six turkey hens were either ES at the neck in a saline bath (570 V, 450 mA, AC, 60 Hz, 2 s on 1 s off for 10 pulses) or used as unstimulated controls. One breast fillet from all carcasses was harvested at 2 h postmortem. The opposite fillet was harvested from the ES carcasses at 8 h postmortem and from the unstimulated controls at either 8 or 24 h postmortem. All fillets were sampled at time of deboning for expressible moisture, pH, R-value, gravimetric fragmentation index (GFI), and sarcomere length. The remainder of the fillet and the samples for GFI and sarcomere length were aged on ice until 24 h postmortem. After aging, fillets were analyzed for cook loss and shear value. Color was measured at time of deboning and at 24 h postmortem. Electrical stimulation accelerated rigor mortis development as indicated by significantly lower pH values and higher R-values at 2 h postmortem when compared to control fillets. The pH and R-values of the 2-h ES treatment were not significantly different from the 8-h ES, 8-h controls, or the 24-h controls. Fillets from carcasses that were ES and deboned at 2 h had significantly longer sarcomeres than the 2-h controls; however, there were no significant differences between the 2-h ES and the 8-h ES treatments, 8-h controls, or the 24-h controls. Although ES accelerated muscle metabolism at 2 h postmortem, it had no effect on shear value, expressible moisture, cook loss, GFI, L*, or a* color values. These results suggest that this postmortem ES system would not benefit turkey processors.

Injection marination strategies for remediation of pale, exudative broiler breast meat.

Pale, soft, and exudative (PSE) breast meat is caused by a rapid postmortem pH decline while carcass temperatures are still warm. The resulting protein denaturation leads to a pale color and a decrease in water-holding capacity, causing excessive yield losses to producers. If some of this protein damage could be prevented or reversed, and water-holding capacity increased, these excessive yield losses could be avoided. Therefore, this study evaluated the use of prerigor injection of broiler breast fillets with sodium phosphates (STPP) and sodium bicarbonate to determine the effects on PSE and normal meat. A total of 200 prerigor broiler breast fillets were collected at 2 h postmortem (PM) at a commercial processing plant and were classified by L* value as pale (L* >54) or normal (L*<51). The fillets were then injected (about or less than 3 h postmortem) with 7% (wt/wt) of 0.54% NaCl + 0.42% PO4 (pH 9), 0.54% NaCl + 0.42% PO4 (pH 11), 0.30 M sodium bicarbonate (pH 12), or left as noninjected controls. The pH and L* value at 2 and 24 h postmortem, marinade uptake, water-holding capacity, and expressible moisture were evaluated. As expected, the pale fillets had lower pH and higher L* values at 2 h postmortem and lower water-holding capacity than the normal fillets. Prerigor marination with NaCl and STPP (pH 9) reduced cook loss in breast fillets. The pH 11 marinade increased 24 h pH of pale fillets compared to that of normal fillets and reduced cook loss. Sodium bicarbonate increased pH at 24 h PM of pale fillets but not to that of normal fillets. These results indicate that marinating prerigor PSE meat with the high-pH phosphate marinade used in this study can improve PSE meat quality.

Bleedout efficiency, carcass damage, and rigor mortis development following electrical stunning or carbon dioxide stunning on a shackle line.

In Experiment 1, 400 male broilers were stunned using a gradient of 40 to 60% CO2 over a period of 25 s or a 1% brine solution that was electrically charged (35 mA) for 7 s. Blood loss during bleeding was measured in 30-s intervals for a total of 120 s. After conventional processing and chilling, carcass damage was subjectively evaluated. Results indicated that the birds stunned with electricity bled faster than the CO2-stunned birds until 60 s. However, the cumulative blood loss was not different after 90 s. Carcass damage evaluation indicated that birds stunned with CO2 had a significantly lower percentage of broken clavicles, and had fewer hemorrhages on the surface of the Pectoralis. However, there was no difference between the two stunning methods in the frequency of damage at the shoulder. In Experiment 2, 256 broilers were stunned using the same conditions as in Experiment 1. Measurements of pH, R-value, sarcomere length (SL), and fragmentation index (FI) were evaluated from the left breast fillets harvested at 0, 1, 2, and 6 h postmortem. Shear values (SV) were determined using the right fillets harvested at the same four postmortem times and aged on ice until 24 h. No significant difference in breast muscle pH value was observed at 0, 2, and 6 h postmortem. However, CO2-stunned fillets had significantly higher pH values than the ES fillets at 1 h postmortem. Carbon dioxide produced greater R values than electricity at 2 and 6 h. Sarcomere length, FI, and SV were not significantly different at any time tested. These data suggest that CO2 stunning reduced carcass damage but did not reduce the need for aging before deboning when compared to the electrical stunning method used.