Effect of carbon monoxide and high oxygen modified atmosphere packaging and phosphate enhanced, case-ready pork chops

The objective of this study was to evaluate the effects of CO-MAP compared to traditional high oxygen MAP (HiOx-MAP) packaging and enhanced with different phosphate on enhanced pork quality. Pork loins were enhanced to 10.5% over initial weight to contain 0.3% salt and 0.4% phosphate (either sodium tripolyphosphate [STP] or a blend of STP and sodium hexametaphosphate) on a finished weight basis. Chops were cut, packaged in atmospheres containing 0.4% CO/30.0% CO₂/69.6% N₂ (CO-MAP) or 80% O₂/20% CO₂ (HiOx-MAP), aged in the dark, then placed in a lighted retail display case for 48 h. Chops packaged in CO-MAP were redder (higher Minolta a^* values) and darker (lower Minolta b^* values) than chops packaged in HiOx-MAP. Based on sensory scores, the CO-MAP chops were pinker than the HiOx chops after cooking. CO-MAP chops also experienced less purge loss than chops in HiOx-MAP. Results indicate that CO-MAP had no effect on flavor or consumer acceptability and only minimal effects on other characteristics.     

Influence of carbon monoxide in package atmospheres containing oxygen on colour, reducing activity, and oxygen consumption of five bovine muscles

Steaks from five bovine muscles [psoas major (PM), longissimus lumborum (LL), deep semimembranosus (DSM), superficial semimembranosus (SSM), and semitendinosus (ST)] were packaged in atmospheres containing 20% or 80% oxygen, with and without 0.4% carbon monoxide. Steaks were evaluated on d 0, 4, and 7 of retail display for instrumental (CIE L^∗, a^∗, and b^∗) and visual colour, total- and metmyoglobin-reducing activity, and oxygen consumption rate. Combining carbon monoxide with either oxygen level had no effect (P > 0.05) on any measured attribute. Using higher oxygen levels increased colour stability and reduced variability (P < 0.05) among muscles for all measured attributes. In general, colour stability and reducing activity for the muscles were LL > ST > SSM > PM > DSM. Including 0.4% carbon monoxide with 20% or 80% oxygen may not have impacted colour, due to preferential formation of oxymyoglobin, rather than carboxymyoglobin, at these oxygen levels.     

The effect of modified atmosphere packaging with carbon monoxide on the storage quality of master-packaged fresh pork

Modified atmosphere packaging with carbon dioxide is effective for prolonging shelf-life of fresh meat. Addition of carbon monoxide to the system provides the advantage of enhancing meat colour. The study objective was to determine the effect of CO₂-MAP + 0.4% CO, vs. 100% CO₂-MAP, on the bacteriology and colour of retail-ready fresh pork stored for 8 weeks in a master-package system. Total plate counts were not affected and listeria was present on meat from both treatments. Colour was enhanced with the inclusion of CO, while no effect on lipid oxidation was observed. Use of CO in MAP provides sufficient storage life and product colour quality to permit shipment of fresh pork to distant markets. However, given the stable fresh colour of CO-treated meat and the lack of inhibition of pathogen growth by CO, there is concern that CO-MAP under certain conditions may pose a food safety risk.     

Color stability of ground beef packaged in a low carbon monoxide atmosphere or vacuum

Ground beef was either packaged in an atmosphere of 0.4% CO, 30% CO₂, and 69.6% N₂ (CO-MAP) or vacuum. After storage (48 h, 2–3 °C), packages of CO-MAP and vacuum were opened and overwrapped with polyvinyl chloride. Other CO-MAP and vacuum packages were left intact. Packages were initially displayed for 7 days (2–3 °C). Intact packages were further displayed up to 35 days before being opened and displayed (1 or 3 days). Intact CO-MAP packaged ground beef was always more red than intact vacuum-packaged ground beef. Color was relatively stable for both types of intact packages over 35 days of display. Upon opening CO-MAP packaged ground beef, the red color decreased slower than in ground beef from vacuum packages.     

Color stability and reversion in carbon monoxide packaged ground beef

This study investigated the relationship between length (1, 2, 4, or 6 days) of exposure to carbon monoxide (CO) and the subsequent rate of loss of carboxymyoglobin color during display (0, 24, 48, 72 h) after repackaging in an oxygen permeable polyvinyl chloride (PVC) overwrap. In addition, the ability of CO to cause color reversion of metmyoglobin to carboxymyoglobin in brown colored, aged (4 days, PVC) or low oxygen-induced (2 days, (LOX-MAP) ground beef was studied. Extending CO exposure time increased overall mean redness. However, overall mean redness decreased after packages were opened. Day 6 exposed ground beef only maintained about 1.5 Minolta a∗ units higher than day 1 exposed after opened 72 h. The color of brown ground beef was converted to carboxymyoglobin upon exposure to carbon monoxide, regardless of how the initial brown color was formed. This color changes was relatively faster in LOX-MAP packaged ground beef compared to that formed by aging in PVC. Although color reversion is possible, consideration should be given to the microbiological status of the ground beef at the time of CO packaging.     

含CO气调包装对冷却肉肉色的影响

以宰后冷却24h的猪背最长肌为材料,用四组含不同浓度CO的混合气体进行气调包装,于4±1℃下贮藏,分别在第0、5、1O、15、20天测定相关指标。结果表明：CO气调包装能明显改善肉色,并使冷却内在贮藏期中保持稳定的鲜红色。与无氧组相比,CO和O2的共同存在可以使冷却肉肉色更加自然。     

Role of lactate dehydrogenase in metmyoglobin reduction and color stability of different bovine muscles

The role of lactate dehydrogenase (LDH) in metmyoglobin reducing activity (MRA) and color stability of different bovine muscles was studied in two consecutive experiments. In experiment 1, three different bovine muscles – M. longissimus lumborum (LL), M. semimembranosus (SM), and M. psoas major (PM) – were obtained (n = 7, respectively), cut into steaks, PVC packaged, and then displayed for 7 days at 1 °C. The LL was the most red over display time and had more (P < 0.05) LDH-B activity (catalyzing toward NADH generation), LDH1 isoform expression, NADH, and higher (P < 0.05) MRA than the other two muscles studied. The PM had the least color stability and lowest MRA. In experiment 2, LL steaks (n = 8) were cut in half, one side syringe-injected with oxamate, and the other injected with distilled water. Inclusion of oxamate decreased (P < 0.05) LDH-B activity, NADH, and a* values after 10 days display at 1 °C. These results suggest that variation in color stability of physiologically different muscles is regulated by different replenishment rates of NADH via different LDH isozymes.     

Composition and color stability of carbon monoxide treated dried porcine blood

Color stability of swine blood was studied over 12 weeks of storage in plastic bags, after pH (7.40, 6.70, or 6.00) adjustment, saturation with carbon monoxide (CO) and spray-drying. CO-treated dried blood presented a redder color and higher reflectance between 610 and 700 nm, compared to a brownish-red color and lower reflectance of untreated samples. As indicated by reflectance spectra, blood pH adjustment did not influence (P > 0.05) the initial color of dried blood but influenced (P < 0.05) its color stability (browning index). During storage, CO-treated blood showed a reduction in reflectance percentages as well as in CIE L^∗ and a^∗ values, which was more pronounced in polyethylene (OTR = 4130 cm³/m²/day/atm) packaged samples. After 12 weeks of storage, CO-treated samples packaged in high OTR bags presented color indexes similar to those of the untreated dried samples. CO-treated samples packaged in nylon-polyethylene (OTR = 30–60 cm³/m²/day/atm) bags showed a smaller rate of discoloration and color difference (ΔE^∗) between the CO-treated and untreated samples. Even with some darkening, packaging CO-treated dry blood in low OTR bags still gives an acceptable reddish color after 12 weeks of storage while untreated dry blood has a brownish color just after drying.     

Beef shelf life in low O(2) and high CO(2) atmospheres containing different low CO concentrations

The use of atmospheres with low concentrations of CO (0.1 to 1%), in combination with O₂ (24%), high CO₂ (50%) and N₂ (25 to 25.9%), for preserving chilled beef steaks was investigated. The atmosphere used as reference contained 70% O₂+20% CO₂+10% N₂. Bacterial counts showed that all atmospheres containing CO greatly reduced total aerobic population numbers, including Brochothrix thermosphacta. Lactic acid bacteria, however, were not affected. CO concentrations of 0.5–0.75% were able to extend shelf life by 5–10 days at 1±1°C, as demonstrated by delayed metmyoglobin formation (less than 40% of total myoglobin after 29 days of storage), stabilisation of red colour (no change of CIE a* and hue angle after 23 days), maintenance of fresh meat odour (no variation of sensory score after 24 days) and significant (P<0.01) slowing of oxidative reactions (TBARS).     

CO气调包装对冷却猪肉货架期及色泽的影响

冷却猪肉采用不同浓度CO气调包装和真空包装,(4±1)℃下贮藏,研究CO气调包装对其货架期和色泽的影响。结果表明,CO气调包装肉在贮藏到第25天时,TVB-N值已超过0.15mg/g,细菌总数超过106cfu/g,与真空包装相比,并不能显著地延长肉的货架期;CO气调包装肉在贮藏期中一直保持稳定的鲜红色,不同浓度CO气调包装对肉色无显著性差异,真空包装肉呈褐色或暗紫色。     

The effects of high oxygen modified atmosphere packaging on protein oxidation of bovine M. longissimus dorsi muscle during chilled storage

Modified atmosphere packaging (MAP) extends the shelf life of beef, especially in the context of visual colour. High O₂ MAP (70-80%) may cause quality deterioration through lipid and protein oxidation, the latter linked to a reduction in meat tenderness. The objective of this study was to investigate the effects of MAP in comparison to vacuum packaging (VP) on protein oxidation and subsequent tenderness of LD (M. longissimus dorsi) beef steaks during chilled storage (4 °C) of periods up to 14 days. Steaks were analysed for carbonyl content, free thiol groups, drip loss, Warner-Bratzler shear force (WBSF) and SDS-PAGE of extracted myofibrillar proteins. Free thiol groups were lower in high O₂ MAP (80% O₂/20% CO₂) steaks, after 14 days of storage, indicating protein oxidation compared to VP steaks. SDS-PAGE (non reducing conditions) showed the presence of high molecular weight cross linked myosin heavy chain aggregates in the high O₂ atmosphere packaged steaks, which were absent in VP steaks.     

Biochemical and physical factors affecting discoloration characteristics of 19 bovine muscles

Steaks from muscles (n = 19 from nine beef carcasses) were evaluated over the course of retail display (0-, 1-, 2-, 3-, 4- or 5-d) for objective measures of discoloration (metmyoglobin, oxymyoglobin, L*-, a*-, and b*-values), reducing ability (metmyoglobin reductase activity (MRA), resistance to induced metmyoglobin formation (RIMF), and nitric oxide metmyoglobin reducing ability (NORA)), oxygen consumption rate (OCR), oxygen penetration depth, myoglobin content, oxidative rancidity, and pH. Muscles were grouped according to objective color measures of discoloration. M. longissimus lumborum, M. longissimus thoracis, M. semitendinosus, and M. tensor fasciae latae were grouped as “high” color stability muscles, M. semimembranosus, M. rectus femoris, and M. vastus lateralis were grouped as “moderate” color stability muscles, M. trapezius, M. gluteus medius, and M. latissimus dorsi were grouped as “intermediate” color stability muscles, M. triceps brachi – long head, M. biceps femoris, M. pectoralis profundus, M. adductor, M. triceps brachi – lateral head, and M. serratus ventralis were grouped as “low” color stability muscles, and M. supraspinatus, M. infraspinatus, and M. psoas major were grouped as “very low” color stability muscles. Generally, muscles of high color stability had high RIMF, nitric oxide reducing ability, and oxygen penetration depth and possessed low OCRs, myoglobin content, and oxidative rancidity. In contrast, muscles of low color stability had high MRA, OCRs, myoglobin content, and oxidative rancidity and low RIMF, NORA, and oxygen penetration depth. Data indicate that discoloration differences between muscles are related to the amount of reducing activity relative to the OCR.     

Effect of carbon monoxide in modified atmosphere packaging, storage time and endpoint cooking temperature on the internal color of enhanced pork

The objective of this research was to evaluate the effects of gas atmosphere, refrigerated storage time, and endpoint temperature on internal cooked color of injection-enhanced pork chops. Enhanced chops were packaged in 0.36% CO/20.34% CO₂ (CO-MAP), 80% O₂/20% CO₂ (HO-MAP), or PVC-overwrapped (PVC-OW; controls), stored at 4 °C for 0, 12, 19 or 26 days, displayed for 2 days then cooked to six endpoint temperatures (54, 60, 63, 71, 77, and 82 °C). L^*, a^*, and b^* values, hue angle and chroma were determined on the internal cut surface of cooked chops. Chops packaged in CO-MAP had the highest a^* values; a^* value began increasing on day 14. The lowest hue angles occurred in chops cooked to lower endpoint temperatures. Chops in CO-MAP had lower hue angles and higher chroma than those in HO-MAP and PVC-OW. Above 71 °C, hue angle and chroma increased. Overall, CO-MAP packaged chops stored for longer time periods then cooked to lower endpoint temperatures appeared reddest. HO-MAP packaged chops were less red, did not change over time, and appeared more well done at lower endpoint temperatures than those in other gas atmospheres. CO-MAP packaged chops retained redness even after cooking at 82 °C.     

Packaging-specific influence of chitosan on color stability and lipid oxidation in refrigerated ground beef

We examined the influence of chitosan on lipid oxidation and color stability of ground beef stored in different modified atmosphere packaging (MAP) systems. Ground beef patties with chitosan (1%) or without chitosan (control) were packaged either in high-oxygen MAP (HIOX; 80% O₂ + 20% CO₂), carbon monoxide MAP (CO; 0.4% CO + 19.6% CO₂ + 80% N₂), vacuum (VP), or aerobic packaging (PVC) and stored at 1 °C. Chitosan increased (P < 0.05) redness of patties stored in PVC and CO, whereas it had no effect (P > 0.05) in HIOX. Chitosan patties demonstrated lower (P < 0.05) lipid oxidation than controls in all packaging. Control patties in PVC and HIOX exhibited greater (P < 0.05) lipid oxidation than those in VP and CO, whereas chitosan patties in different packaging systems were not different (P > 0.05) from each other. Our findings suggested that antioxidant effects of chitosan on ground beef are packaging-specific.     

High-oxygen modified atmosphere packaging system induces lipid and myoglobin oxidation and protein polymerization

Beef steaks from longissimus lumborum, semimembranosus, and adductor muscles (n = 10; respectively) were cut at 24 h postmortem, randomly assigned to either high-oxygen modified atmosphere packaging (HiOx-MAP; 80% O₂, 20% CO₂) or vacuum (VAC), and displayed for 9 days at 1 °C. HiOx-MAP packaged beef steaks had a rapid increase in lipid oxidation and a decrease in color stability during display. The steaks in HiOx-MAP had significantly lower tenderness and juiciness scores, and higher off-flavor scores compared to steaks in VAC. HiOx-MAP condition did not affect the postmortem degradation of troponin-T or desmin. Furthermore, autolysis of μ-calpain was not influenced by packaging. SDS–PAGE, immunoblotting, and diagonal-PAGE revealed oxidative cross-linking of myosin heavy chain in meat packaged in HiOx-MAP. These results suggest that the HiOx-MAP system may negatively affect meat quality characteristics by inducing lipid and myoglobin oxidation and cross-linking/aggregation of myosin by protein oxidation.     

Effect of high carbon dioxide atmosphere packaging and soluble gas stabilization pre-treatment on the shelf-life and quality of chicken drumsticks

The effects of an aerobic modified atmosphere packaging (MAP) (70% CO₂, 15% O₂ and 15% N₂) with and without a CO₂ 3-h soluble gas stabilization (SGS) pre-treatment of chicken drumsticks were determined for various package and product quality characteristics. The CO₂ dissolved into drumsticks was determined. The equilibrium between CO₂ dissolved in drumsticks and CO₂ in head space was reached within 48 h after packaging, showing highest values of CO₂ in SGS pre-treated samples. This greater availability of CO₂ resulted in lower counts of TAB and Pseudomonas in SGS than in MAP drumsticks. Package collapse was significantly reduced in SGS samples. The average of CO₂ dissolved in the MAP treatment was 567 mg CO₂ kg^− 1 of chicken and, 361 mg CO₂ kg^− 1 of chicken during the MAP treatment, in SGS pre-treated samples. This difference could be the quantity of CO₂ dissolved during SGS pre-treatment.     

Influence of vacuum skin packaging on color stability of beef longissimus lumborum compared with vacuum and high-oxygen modified atmosphere packaging

The objective of this study was to investigate how color stability of beef is affected by vacuum skin packaging (VSP) compared with vacuum packaging (VP) and high-oxygen modified atmosphere packaging (MAP; 80% O(2) and 20% CO(2)). Longissimus lumborum muscles were aged in vacuum for 7days and then cut into 2-cm-thick slices and repacked using VSP, VP and MAP for another 7days. Color stability was measured during the next 5days in air and samples for α-tocopherol and NADH analyses were obtained at the beginning and end of aerobic storage. Color stability, α-tocopherol and NADH of steaks were affected by packaging methods and storage time in air (P<0.05). Higher a* value was obtained in VSP on day 5 compared with VP. Steaks packed in VSP had better color stability than in VP and their color was similar to MAP at the end (day 5) of storage.     

Colour stability of beef from different Spanish native cattle breeds stored under vacuum and modified atmosphere

Beef steaks from five Spanish cattle breeds were submitted to three packaging conditions: (a) 15 days under vacuum, (b) 15 days under modified atmosphere (MAP) (60% O₂, 30% CO₂ and 10% N₂), and (c) 10 days under vacuum plus 5 days more under MAP. CIE L^*a^*b^* coordinates, chroma (C^*) and hue (H^*), relative concentration of myoglobin, oxymyoglobin and metmyoglobin at the meat surface and sensory evaluation of colour were determined 0, 5, 10 and 15 days after packaging. Beef under MAP showed higher lightness (L^*) and hue (H^*) and lower redness (a^*) and chroma (C^*) than beef under vacuum. Colour of beef under MAP was not acceptable after 15 days of storage, due to the high metmyoglobin concentration. Yellowness (b^*) was the indicator of differences due to ageing and differences in colour between breeds were related to L^*, a^* and H^* values. Packaging conditions had a greater effect on beef colour than breed, but breed differences might change with packaging atmosphere. Both packaging and breed are major factors in packaged beef quality.     

Storage and packaging effects on sensory and color characteristics of ground beef

Effects of irradiation (2 kGy) of ground beef patties from trimmings stored aerobically for 0 or 6 days on lean color, odor, and sensory attributes were investigated. Beef trimings were coarse ground and split into 2 groups. Group one was fine ground, pattied, and packaged immediately; group-two was stored 6 days then fine ground, pattied, and packaged. Irradiated beef patties had greater (P<0.05) off-odors, and off-flavors, lower (P<0.05) CIE L^*, a^* and b^* and saturation indexes values (P<0.05) after four days of storage at 0±1 °C. Irradiation of patties produced from trimmings aged an extra 6 days resulted in increased (P<0.05) saturation indexes and b^* values, but not off-odors when compared to non-aged and irradiated patties. Thus, the production of irradiated beef patties should utilize beef trimmings with the shortest postmortem aging time and a dose of less than 2 kGy to minimize discoloration and off-odors.     

Effect of high-oxygen atmosphere packaging on mechanical properties of single muscle fibres from bovine and porcine <Emphasis Type="Italic">longissimus dorsi</Emphasis>

The effect of storage in high-oxygen atmosphere packaging for 48 h at 4 °C on the myofibrillar component of meat toughness was studied performing tensile tests on single muscle fibres, isolated from beef and pork longissimus dorsi (LD). Storage of bovine LD for 48 h in the presence of oxygen significantly increased the breaking strength of single muscle fibres when compared with storage in a 100% nitrogen atmosphere. In contrast, the breaking strength of porcine LD stored for 2 days post-mortem in the presence of oxygen in the packages was not influenced.