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dc.contributor.advisorSavell, Jeffrey W
dc.creatorKim, Yuan Hwan
dc.date.accessioned2010-01-15T00:11:20Z
dc.date.accessioned2010-01-16T01:09:03Z
dc.date.available2010-01-15T00:11:20Z
dc.date.available2010-01-16T01:09:03Z
dc.date.created2008-08
dc.date.issued2009-05-15
dc.identifier.urihttps://hdl.handle.net/1969.1/ETD-TAMU-2966
dc.description.abstractThe primary objectives of this research were to characterize the involvement of lactate dehydrogenase (LDH) in color stability of physiologically different bovine muscles, and to investigate the influence of lactate enhancement on the myoglobin redox state of bovine muscles. In experiment 1, three different bovine muscles; Longissimus lumborum (LD), Semimembranosus (SM), Psoas major (PM) were (n=7 respectively) cut into steaks, and displayed for 7 days. Instrumental color, LDH-B, LDH isozyme expression, and NADH were measured. In experiment 2, strip steaks (n=8) were cut into half, and one side was injected with oxamate (LDH inhibitor), and the other was injected with water. Surface color, LDH, and NADH were measured after 10 days. In experiment 3, the three bovine muscles (n=10) were enhanced with solutions containing lactate and/or phosphate. Steaks were stored and displayed for 14 days. Instrumental color, LDH-B, total reducing activity (TRA), and NADH were measured. In experiment 4, fifteen beef strip loins were divided individually into four equal sections, and one of six treatments containing phosphate and/or calcium lactate with or without irradiation (2.4 kGy) randomly assigned to each loin section (n=10). Steaks were packaged in highoxygen modified atmosphere package, irradiated, stored in the dark at 1°C for 14 days. Instrumental color, TRA, lipid oxidation, and NADH were measured. LD remained the most red, whereas PM was most discolored. LD had a significantly higher level of LDH-1 responsible for LDH-B activity as compared to SM and PM. Consequently, LD had a higher LDH-B, and more NADH (p < 0.05). Inclusion of oxamate inhibited LDH-B, decreased NADH, and consequently discolored more. Potassium lactate enhancement led to more NADH through elevated LDH flux and subsequently increased (p < 0.05) color stability of LD and PM throughout display. Loins with calcium lactate/phosphate maintained the most stable red color during display. Calcium lactate/phosphate in loins increased NADH concentration, TRA, and were the least oxidized over display. These results confirm the involvement of LDH in meat color stability through replenishment of NADH. Lactate enhancement promotes meat color stability by providing superior antioxidant capacity and increased reducing activity of myoglobin by elevating NADH concentration.en
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.subjectLDHen
dc.subjectcoloren
dc.subjectbeefen
dc.subjectlactateen
dc.titleLactate dehydrogenase regulation of the metmyoglobin reducing system to improve color stability of bovine muscles through lactate enhancementen
dc.typeBooken
dc.typeThesisen
thesis.degree.departmentAnimal Scienceen
thesis.degree.disciplineFood Science and Technologyen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.levelDoctoralen
dc.contributor.committeeMemberBerghman, Luc R
dc.contributor.committeeMemberKeeton, Jimmy T
dc.contributor.committeeMemberSmith, Steve B
dc.type.genreElectronic Dissertationen
dc.type.materialtexten
dc.format.digitalOriginborn digitalen


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