Turkey Breast Rolls Research Articles

Effect of irradiation on the parameters that influence quality characteristics of uncured and cured cooked turkey meat products

The objective of this study was to evaluate the effect of irradiation on lipid/protein oxidation, color changes, and off-odor volatiles production in uncured and cured cooked turkey meat products. Uncured cooked turkey breast meat and cured commercial turkey breast rolls and ham were prepared and irradiated at 0, 1.5, 3.0, and 4.5 kGy using a linear accelerator. The results showed that irradiation had little effects on lipid oxidation of cured cooked turkey products, but accelerated lipid oxidation in uncured cooked turkey breast meat (P < 0.05). Protein oxidation was increased both in cured and uncured meats (P < 0.05), but more in cured cooked meat by irradiation. The redness of uncured cooked turkey was increased (P < 0.05), but the redness of cured cooked turkey meat was faded by irradiation (P < 0.05). Irradiated cured cooked turkey meat products produced less off-odor volatile compounds (dimethyl disulfide, 3-methyl/2-methyl-butananl, and hexanal) than irradiated uncured cooked meat products due to various additives in the cured meat products. Our results suggested that irradiation resulted in different chemical reactions to pigments in uncured and cured cooked turkey meat products, but cured cooked turkey meat products have a higher tolerance to odor deterioration than uncured cooked turkey meat products.

Fate of Listeria monocytogenes in ready-to-eat turkey breast rolls formulated with antimicrobials following electron-beam irradiation

The objective of this study was to determine the effect of antimicrobials on the survival and proliferation of Listeria monocytogenes in turkey breast rolls following electron-beam irradiation. Six antimicrobial additive treatments that include no preservatives (control), 0.1% potassium benzoate (PB), 2% sodium lactate (SL), 0.1% potassium benzoate plus 2% sodium lactate (PB + SL), 2% sodium lactate plus 0.1% sodium diacetate (SL + SDA), and 0.1% potassium benzoate, 2% sodium lactate, and 0.1% sodium diacetate (PB + SL + SDA) were used. Sliced turkey breast rolls were artificially inoculated with approximately 10(6) cfu/cm(2) of 5-strain L. monocytogenes cocktails, then vacuum-packaged and irradiated at 0, 1.0, 1.5, 2.0, or 2.5 kGy. The radiation dose (kGy) that results in 90% reduction of viable cells for breast rolls, D(10) value, with various additive treatments ranged from 0.56 to 0.58 kGy. Adding PB (0.1%) or SL (2%) in turkey rolls failed to prevent L. monocytogenes from growing during refrigerated storage. In turkey rolls added with 2 (PB + SL or SL + SDA) or 3 (PB + SL + SDA) antimicrobial combinations had 2 or 3 wk of lag phases before L. monocytogenes growth, respectively. Irradiating turkey rolls, which were added with PB + SL or SL + SDA, at 1.0 kGy was effective in suppressing the growth of L. monocytogenes for about 6 wk when stored at 4 degrees C. No growth of L. monocytogenes after irradiation occurred during 42 d of storage for 2.0 kGy irradiated breast rolls formulated with 0.1% PB + 2% SL, 2% SL + 0.1% SDA or 0.1% PB + 2% SL + 0.1% SDA, and 1.0 kGy irradiated turkey breast with 0.1% PB + 2% SL + 0.1% SDA. Sensory panelists found that low-dose irradiation (1.0 kGy) had no effect on the sensory characteristics of ready-to-eat turkey breast rolls. Including SL + SDA had slightly negative effect for nonirradiated turkey breast rolls, but the sensory characteristics of 1.0 kGy irradiated turkey roll containing SL + SDA was not significantly different from the others receiving 1.0 kGy irradiation. For microbial safety, PB + SL and SL + SDA antimicrobial treatments combined with 1.0 kGy or 2.0 kGy irradiation are a promising technology.

Effects of Irradiation on Survival and Growth of Listeria monocytogenes and Natural Microflora in Vacuum-Packaged Turkey Hams and Breast Rolls

The effect of electron beam irradiation on the survival and growth of Listeria monocytogenes and natural microflora in oven-roasted turkey breast rolls and turkey hams was evaluated. Slices of turkey breast rolls and hams were inoculated with a 5-strain mixture of L. monocytogenes to achieve 106 to 107 cfu/cm2; vacuum-packaged; irradiated at 0 (control), 1.0, 1.5, 2.0, or 2.5 kGy; and stored at 4°C for up to 28 d. Numbers of naturally occurring bacteria on sliced turkey hams and breast rolls were 2.72 and 6.22 log10 cfu/cm2, respectively. The values of the radiation dose that results in 90% reduction of viable L. monocytogenes in breast rolls and hams were 0.52 and 0.47 kGy, respectively. For breast rolls, the log10 reductions of L. monocytogenes after irradiation at 1.0 and 2.5 kGy were 1.5 and 4.7, respectively, whereas they were 2.0 and 5.5 for hams. The log10 reductions of aerobic plate count (APC) in breast rolls after 1.0 and 2.0 kGy of irradiation were 2.9 and 5.2, whereas that of hams was <10 cfu/cm2 after 1.0 and 2.0 kGy of irradiation. In 2.0-kGy irradiated hams, L. monocytogenes grew to 4.82 log10 cfu/cm2 after 28 d of storage at 4°C, whereas APC increased to 2.98 log10 cfu/cm2, respectively. In breast rolls after 14 d of storage, APC in 1.0-kGy irradiated samples increased to 7.53 log10 cfu/cm2, and APC increased to 2.63 and 4.68 log10 cfu/cm2 for 2.0-kGy irradiated breast rolls after 14 and 28 d of storage. However, during the storage of breast rolls, L. monocytogenes grew slowly or even stopped to grow in both nonirradiated and irradiated breast rolls due to the competitive inhibition of natural flora in breast rolls. This study showed that irradiation (1.0 to 2.5 kGy) effectively reduced the number of L. monocytogenes and natural flora. However, L. monocytogenes and natural flora that survived irradiation could multiply during the 28-d storage period at 4°C. Thus, additional hurdles are needed to ensure the microbial safety after low-dose irradiation.

The effects of brined onion extracts on lipid oxidation and sensory quality in refrigerated cooked turkey breast rolls during storage

The effects of brined onion extracts on selected aspects of quality in cooked encased turkey breast rolls were evaluated during refrigerated storage over 7 days. Using the thiobarbituric acid (TBA) assay, a 50% strength juice gave a significant reduction ( P < 0.0001) in lipid oxidation in both 100 g and 1 kg rolls relative to controls. Quercetin, the main onion juice antioxidant, was reduced by 65% in freshly cooked 1 kg rolls compared with raw rolls but changed little thereafter in storage. Cook yields were significantly higher for rolls containing added onion extracts than for controls ( P < 0.05) but no colour differences were detected using Hunter Lab values ( P ⩾ 0.05). A 30-member untrained sensory panel expressed no preference for freshly opened 4 day-stored control or onion extract-supplemented rolls packed in plastic casings but there was a significant preference ( P < 0.05) for the onion extract product when 4 mm thick meat slices were stored in air for an additional 24 h.

Quality characteristics of irradiated turkey breast rolls formulated with plum extract

The effects of adding 1%, 2% and 3% plum extract on the quality characteristics of vacuum-packaged, irradiated ready-to-eat turkey breast rolls were determined. Turkey breast rolls were sliced, packaged and irradiated at 0 or 3 kGy using a Linear Accelerator. Lipid oxidation, volatile profiles, color, texture, proximate analysis and sensory characteristics of sliced turkey breast rolls were determined at 0 and 7 days of storage. Addition of plum extract had no detectable effect on the proximate analysis of turkey breast rolls. Plum extract increased a* and b* values, and decreased L* value of turkey breast rolls due to the original color of plum extract. Addition of >2% plum extract to turkey breast rolls was effective in controlling lipid oxidation of irradiated meat and the production of aldehydes (hexanal, heptanal, octanal, and nonanal) in non-irradiated meat at Day 0. Texture of turkey breast rolls was not influenced, but juiciness was increased by plum extract. Therefore, addition of 3% or higher of plum extract is recommended to improve mouth-feel and antioxidant effect in irradiated turkey breast rolls. However, the color of turkey breast rolls with 3% plum extract was dark and might not be appealing to consumers.

The effect of radio frequency heating on chemical, physical and sensory aspects of quality in turkey breast rolls

The effects of radio frequency (RF) heating on the chemical, physical and sensory properties of large diameter encased turkey breast rolls were compared to those of the same products cooked in a conventional steam oven. The time to endpoint temperature (minimum 73 °C) for an RF-cooked product at 500 W was 40 min as compared to 150 min for a steam-cooked product. Proximate analysis of macro components, assays of the B-vitamins, thiamine and riboflavin, and texture profile analysis (TPA) revealed no significant difference ( P ⩾ 0.05) between the two cooking methods. However, RF-cooked turkey rolls had lower Hunter a values (redness) than their steam cooked counterparts. In addition, the rate of lipid oxidation in RF-cooked rolls, during refrigerated storage at 5 °C, was significantly slower than in the steam-cooked products. While a sensory panel could distinguish between RF- and steam-cooked rolls, panellists did not express a preference for rolls cooked by either method.

Influence of irradiation and storage on the quality of ready-to-eat turkey breast rolls

Influence of irradiation and storage on the quality of ready-to-eat (RTE) turkey breast rolls was investigated. Commercial oven roasted turkey breast rolls purchased from local stores were sliced and vacuum packaged. The sliced samples were randomly divided into 3 groups and irradiated at 0, 1.0, or 2.0 kGy using a linear accelerator. Color, 2-TBA-reactive substances (TBARS), sensory characteristics, and volatiles were evaluated at 0, 7, and 14 d of storage. Irradiation increased color a* value of turkey breast rolls. Irradiation and storage did not influence TBARS values. Sensory evaluation showed that irradiation significantly increased sulfury flavor. Because a dramatic increase in sulfur compounds was detected in irradiated samples, the sulfury flavor should be due to the sulfur compounds formed during irradiation. Irradiation also increased the amounts of acetylaldehyde, 2-methyl butanal, 3-methyl butanal, benzene, and toluene. It was concluded that irradiation significantly influenced the odor and flavor of RTE turkey breast rolls under vacuum packaging conditions. Therefore, strategies to prevent negative changes in the quality of irradiated RTE turkey breast rolls are needed.

Quality characteristics of irradiated ready-to-eat breast rolls from turkeys fed conjugated linoleic acid

The objective of this study was to determine the effect of irradiation on the quality of ready-to-eat (RTE) breast rolls from turkeys fed conjugated linoleic acid (CLA). The oxidative stability of RTE turkey rolls was improved by the dietary CLA treatment. Irradiation increased the production of acetaldehyde, 3-methyl-butanal, 2-methyl-butanal, and total volatiles in turkey rolls but had little effect on other aldehydes. Irradiation also produced new volatiles, including sulfur compounds, not detected in nonirradiated turkey breast rolls. We detected significantly higher amounts of alkanes with nine or higher carbons in irradiated samples than in nonirradiated samples. Irradiation increased the redness of RTE turkey breast rolls, but the degree of redness and the amount of total volatiles decreased with storage. CLA treatment lowered the redness (a*) and increased the lightness (L*) of RTE turkey breast rolls during the entire storage period. Sensory evaluation revealed that irradiation produced off-flavor, but CLA and irradiation did not influence the texture and juiciness of RTE turkey breast rolls. Consumers did not like the off-flavor but preferred the color induced by irradiation to nonirradiated RTE turkey breast rolls.

IMMUNOASSAYS FOR DETERMINATION OF ENDPOINT PROCESSING TEMPERATURES IN POULTRY AND BEEF PRODUCTS1

ABSTRACTThe United States Department of Agriculture (USDA) requires that meat and poultry products be processed to specific minimum endpoint temperatures (EPT) to ensure destruction of pathogens. Several enzyme‐linked immunosorbent assays (ELISA), using antibodies that recognize different indicator proteins, were developed to verify minimum EPT in several products. These assays are highly specific and can be used by minimally trained personnel to rapidly verify EPT without the need for separation steps or sophisticated scientific equipment necessary with other EPT assays. A sandwich ELISA, using lactate dehydrogenase (LDH) as the marker protein, was used to verify EPT of turkey breast rolls and turkey ham. Two other indirect competitive ELISAs, detecting turkey serum albumin and Immunoglobulin G, were compared for their ability to verify minimum EPT in turkey ham. Self‐contained ELISA field kits can be devised to verify compliance to USDA minimum temperatures in about 30 min or less.

Lactate Dehydrogenase, Serum Protein, and Immunoglobulin G Content of Uncured Turkey Thigh Rolls As Influenced by Endpoint Cooking Temperature

The efficacy of using a lactate dehydrogenase (LDH) sandwich enzyme-linked immunosorbent assay (ELISA), a turkey serum protein sandwich ELISA, and an immunoglobulin G (IgG) competitive indirect ELISA for determining the endpoint cooking temperature of uncured turkey thigh rolls was studied. Serum protein content in extracts was assessed by ELISA and was found to decrease as the cooking temperature increased. Serum protein ELISA differentiated between products cooked to 68.9 and 71.1 o C. Five LDH isozymes were found in raw turkey thigh rolls. In contrast to turkey breast rolls, the LDH ELISA could not differentiate the endpoint temperatures of thigh rolls processed between 68.9 and 71.1 o C due to the presence of three heat-stable isozymes

ELISA Determination of Turkey Roll Endpoint Temperature: Effects of Formulation, Storage, and Processing

ABSTRACTEffects of refrigerated and frozen storage, salt concentration, cooking schedule and product diameter were compared on determination of minimum endpoint cooking temperature of turkey breast rolls by measuring extractable protein (EP), lactate dehydrogenase (LDH) activity and LDH concentration by sandwich enzyme‐linked immunosorbent assay. LDH concentration differed in rolls processed to 70.0°C and 71.1°C, whereas EP and LDH activity did not differ at these temperatures. Salt concentration, cooking schedule and product casing diameter did not markedly influence LDH concentration. LDH content of uncooked rolls decreased during frozen storage. A maximum concentration of 0.31 μg LDH/g meat indicated proper processing.

Lactate Dehydrogenase as Safe Endpoint Cooking Indicator in Poultry Breast Rolls: Development of Monoclonal Antibodies and Application to Sandwich Enzyme-Linked Immunosorbent Assay (ELISA)

A sandwich enzyme-linked immunosorbent assay (ELISA) was developed to detect lactate dehydrogenase (LDH) as a marker protein for verifying endpoint cooking of uncured poultry products. Monoclonal antibodies were prepared against chicken muscle LDH and used with rabbit polyclonal antibodies developed against turkey or chicken muscle LDH for capture and detection in the assay, respectively. Minimum assay detection limits for turkey and chicken muscle LDH were 1 ng/ml. Turkey and chicken muscle LDH, but not LDH from other species cross reacted in the ELISA. The ELISA was further verified using extracts of turkey breast rolls processed to internal temperatures between 68.3 and 72.1°C. The LDH content of extracts diluted 3- to 6-fold was below 15 ng/ml for turkey rolls processed to 70.9 and 72.1°C. At a 6-fold dilution, LDH content of extracts from rolls processed to 69.7°C was approximately 10 times greater than those processed to 70.9°C. A survey of market precooked poultry products indicated assay validity with precooked turkey roast, but not turkey hams with maximum internal temperature requirements of 68.3°C. Results suggested the sandwich ELISA should be applicable for determining whether turkey breast rolls are processed to the required U.S. Department of Agriculture endpoint temperature of 71.1°C.

Stability of Vacuum Cook‐in‐Bag Turkey Breast Rolls during Refrigerated Storage

ABSTRACTVacuum packaged, uncured turkey breast rolls prepared commercially in two plants by the cook‐in‐bag process were evaluated for physicochemical and microbiological stability during 87 days storage at 4°C. Total product weight, drained weight, pH, nonprotein nitrogen and tensile strength of turkey were not significantly affected by storage. Shear strength decreased while thiobarbituric acid numbers increased slightly in the turkey rolls. Hunter aL color values of turkey slices varied inconsistently during storage. No psychrotrophic aerobic colony forming units were detected. Mesophilic anaerobe counts were higher in the meat core than on the surface, thus precautions should be taken to insure vacuum cook‐in‐bag poultry products are not temperature abused.

Influence of Phospholipids on the Development of Oxidized Off Flavors in Cooked Turkey Rolls

ABSTRACTTotal lipid and phospholipid (PL) fractions and their fatty acid profiles were analyzed from the interior and exterior portions of cooked turkey breast rolls. Compositional changes during refrigeration were related to oxidative degradation as measured by the TBA test. Breast tissues contained 2% lipid which remained constant over storage. The PLs constituted 0.7% of the meat and only those PLs in the exterior portion degraded during storage. TBA values increased in both roll portions with a concomitant reduction in polyunsaturated fatty acids (PUFAs) having four or more double bonds. These findings suggested that PUFAs were associated with oxidized off‐flavors in cooked turkey rolls. Phosphatidylcholine was present in the highest concentration and underwent the greatest oxidative deterioration.