Muscle Protein Extractability as Influenced by Conditions of Post-Mortem Glycolysis.

1964 ◽  
Vol 115 (3) ◽  
pp. 823-825 ◽  
Author(s):  
E. J. Briskey ◽  
R. N. Sayre
Meat Science ◽  
1997 ◽  
Vol 45 (3) ◽  
pp. 339-352 ◽  
Author(s):  
R.D. Warner ◽  
R.G. Kauffman ◽  
M.L. Greaser

Foods ◽  
2019 ◽  
Vol 8 (2) ◽  
pp. 60 ◽  
Author(s):  
Yao Zhu ◽  
Anne Mullen ◽  
Dilip Rai ◽  
Alan Kelly ◽  
David Sheehan ◽  
...  

RNAlater® is regarded as a potential preservation method for proteins, while its effect on bovine muscle proteins has rarely been evaluated. Bovine muscle protein samples (n = 12) collected from three tender (Warner–Bratzler shear force: 30.02–31.74 N) and three tough (Warner–Bratzler shear force: 54.12–66.25 N) Longissimus thoracis et lumborum (LTL) samples, preserved using two different sampling preservation methods (RNAlater® and dry ice), at two post mortem time points (day 0 and day 14), were characterized using one-dimensional electrophoresis. Fourteen bands with molecular weights ranging from 15 to 250 kDa were verified, both in the dry ice and RNAlater® storage groups, at each time point, using image analysis. A shift from high to low molecular weight fragments, between day 0 and day 14, indicated proteolysis of the muscle proteins during post mortem storage. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) analyses and database searching resulted in the identification of 10 proteins in four bands. Protein profiles of muscle preserved in RNAlater® were similar to those of muscle frozen on dry ice storage, both at day 0 and day 14. The results demonstrate that RNAlater® could be a simple and efficient way to preserve bovine muscle proteins for bovine muscle proteomic studies.


Meat Science ◽  
2021 ◽  
pp. 108562
Author(s):  
Mateusz Bucław ◽  
Adam Lepczyński ◽  
Agnieszka Herosimczyk ◽  
Małgorzata Ożgo ◽  
Danuta Szczerbińska ◽  
...  

2014 ◽  
Vol 54 (4) ◽  
pp. 375 ◽  
Author(s):  
Yuan H. Brad Kim ◽  
Robyn D. Warner ◽  
Katja Rosenvold

The impacts of accelerated pH decline combined with high muscle temperature on post-mortem muscle metabolism and subsequent meat quality attributes have been extensively studied. Traditionally, this phenomenon has been observed in pork muscles, primarily due to the relatively fast post-mortem glycolysis rate and its relationships to stress susceptibility of pigs before slaughter. However, the protein-denaturing condition of high temperature/rapid pH fall and subsequent PSE (pale, soft and exudative)-like abnormal meat quality characteristics have been observed in muscles from other species such as beef, lamb, venison and even poultry. Various pre-rigor conditions including the application of electrical stimulation, hot-boning, and/or pre-rigor carcass chilling temperatures in various muscles, in conjunction with carcass stretching/hanging methods, can also contribute to muscle-protein denaturation pre-rigor. This review considers the influence of a faster than normal pH fall at a higher than normal pre-rigor temperature on glycolysis, post-mortem muscle proteins and subsequently meat quality attributes. Gaps in current knowledge are identified and recommendations made for additional research.


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