Mn. O'Grady et al., Oxymyoglobin in bovine muscle systems as affected by oxidizing lipids, vitamin E and metmyoglobin reductase activity, J MUSCLE F, 12(1), 2001, pp. 19-35
Oxymyoglobin and lipid oxidation were examined in low and high vitamin E (a
lpha -tocopherol) bovine M. longissimus thoracis et lumborum (LD) homogenat
es and in subcellular fraction of LD. Investigation of the effects of tempe
rature (4, 22, 37C) and pH (5.5, 6.4, 7.2) on lipid and oxymyoglobin oxidat
ion indicated that oxymyoglobin oxidation increased with increasing tempera
ture (P less than or equal to 0.05) and was higher at the low pH (P less th
an or equal to 0.05). Lipid oxidation increased with temperature (P less th
an or equal to 0.05) only at pH 5.5. The inclusion of 45 muM FeCl3/ascorbat
e (1:1), at pH 5.5 and 4C, led to significant increases (P less than or equ
al to 0.05) in lipid oxidation bur significant oxymyoglobin oxidation occur
red only when the extent of lipid oxidation exceeded a threshold level. Oxy
myoglobin and lipid oxidation were significantly lower in LD fractions deri
ved from high vitamin E muscle compared to low vitamin E muscle. alpha -Toc
opherol did not interact directly with oxymyoglobin to suppress oxymyoglobi
n oxidation but a positive unit effect of muscle alpha -tocopherol on metmy
oglobin reductase activity was observed.