28-7 |
Myofibrillar proteomic fingerprints in beef loin at 36 hours postmortem correlated with ultimate carcass tenderness |
S. A. Kaiser, M. Wick, J. C. SAWDY, and N. R. St-Pierre. Dept. of Animal Sciences, Ohio State Univ., 2029 Fyffe Rd., 221-A Animal Sciences Bldg., Columbus, OH 43210
In
beef, tenderness is considered the most important, yet the most variable, of
all palatability characteristics.
Despite the current USDA grading system and branded beef programs
implemented by the beef industry, there continues to be difficulty in accurately
identifying and segregating carcasses into tenderness categories. The industry has identified the development
of an accurate method to predict tenderness as a high priority. The purpose of this study was to employ quantitative
electrophoretic image analysis of bovine longissimus dorsi to
segregate beef carcasses into tenderness categories at the time of grading in
the processing plant. Two
2.5 cm steaks were removed from the loin area from 20 carcasses at the time of
USDA grading, approximately 36 hr postmortem.
One steak was aged and subjected to Warner-Bratzler shear force (WBS)
analysis. The other steak was frozen,
myofibrils extracted, subjected to SDS-PAGE and the gel fluorescently
stained. Gel images were captured,
digitized, normalized, bands quantitated and subjected to analysis by a reverse
stepwise linear regression. This
method was able to correlate postmortem myofibrillar fingerprints and ultimate
WBS analysis with an r2=0.82.
In all, the intensities of seven bands were identified as being either a
positive or negative parameter in a linear equation predicting ultimate WBS
values. These
findings lay the foundation of future strategies for developing consistently
reliable and accurate methods of predicting meat tenderness based on the
understanding of the fundamental cellular mechanisms underlying the proteolytic
breakdown of muscle proteins during the aging process. For instance, the peptides identified by
this method can be removed from the gel, and employed as immunogens or submitted
for amino acid sequencing. This
information could be used to not only develop an immunological method for
determining tenderness but also establish a clearer understanding of the
mechanisms of postmortem development of tenderness.
Session 28, Muscle Foods: General I
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