and Implications Irradiation of ground beef under aerobic conditions oxidized myoglobin and drastically reduced color a*-values. Under vacuum or non-oxygen conditions, however, irradiation did not influence the redness of ground beef. Also, the red color of ground beef was maintained even after the irradiated beef was exposed to aerobic conditions. Vacuum-packaged irradiated ground beef had lower metmyoglobin content and lower oxidation-reduction potential than the aerobically packaged ones. Irradiating ground beef under vacuum-packaging conditions was also advantageous in preventing lipid oxidation and aldehydes production. Vacuum-packaged irradiated beef, however, produced high levels of sulfur volatiles during irradiation and maintained their levels during storage, which resulted in the production of characteristic irradiation off-odor. Double-packaging (V3/A3: vacuum-packaging during irradiation and the first 3 days of storage and then aerobic-packaging for the remaining 3 days) was an effective alternative in maintaining original beef color (red), and minimizing lipid oxidation and irradiation off-odor. The levels of off-odor volatiles in double-packaged irradiated ground beef were comparable to that of aerobically packaged ones, and the degree of lipid oxidation and color changes were close to those of vacuum-packaged ones. Ascorbic acid at 200 ppm level was not effective in preventing color changes and lipid oxidation in irradiated ground beef under aerobic conditions, but was helpful in minimizing quality changes in doublepackaged irradiated ground beef. This suggested that preventing oxygen contact from meat during irradiation and early storage period (V3/A3 double-packaging) and double-packaging+ascorbic acid combination are excellent strategies to prevent off-odor production and color changes in irradiated ground beef. Developing methods that can prevent quality changes of irradiated beef is important for the implication of irradiation, which will improve the safety of beef.
and Implications 2-Thiobarbituric acid-reactive substances (TBARS) values of raw pork, and chicken breast and thigh meats did not change during a 7-d storage period. Low free iron content and high ferric ion reducing capacity (FRC) were responsible for the low TBARS values in those meats during storage. TBARS values of raw beef loin, however, significantly increased during 7-d storage because of high free iron content and high lipoxygenase-like activities by ferrylmyoglobin. The TBARS values of cooked meat increased significantly with storage. Heat-stable FRC was detected in all cooked meat and was responsible for the increase of TBARS in cooked meat during storage. The rate of TBARS increases and the amounts of nonheme iron and heat-stable FRC in cooked beef loin were higher than those in cooked pork loin and chicken breast. In spite of lower amounts of nonheme iron and heat-stable FRC, cooked chicken thigh showed similar levels of TBARS to cooked beef loin after 7-d storage because of its high PUFA content. The total amount of PUFA in meat, most of which were present in triglycerides, influenced the development of lipid peroxidation only in the presence of sufficient amounts of free irons in cooked meat. This indicated that the content of free ionic iron, myoglobin, and ferric ion reducing capacity (FRC) were the primary determinants for the different susceptibility of raw meats to lipid peroxidation. In cooked meat, the contents of free ionic iron and heat-stable FRC played a key role on the development of lipid peroxidation. PUFA was important for lipid oxidation in cooked meat only when sufficient amount of free iron was present.
and Implications At 7 and 14 d postmortem very little troponin-T degradation (30kDa) was seen in the GR, SAR, and VI. However, star probe measurements of GR (d3 and d7), SAR (d7), and VI (d1 and d7) were lower than the LD. The AD showed very little change in the amount of degraded troponin-T. This is mirrored in the star probe results of the AD where very little change is seen over time. The SM and VL were the only muscles to have star probe values higher than the LD. From this we can see that biochemical and tenderness differences exist between different muscles of the round, and some round muscles display biochemical and tenderness characteristics similar to those of the LD. As a result of this there is the potential to add value to some of the muscles (GR, SAR, and VI) of the round by marketing them as individual cuts.
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