Sams A R
Department of Poultry Science, Texas A&M University, College Station 77843-2472, USA.
Poult Sci. 1997 Mar;76(3):543-7. doi: 10.1093/ps/76.3.543.
Biochemical characteristics of spent fowl meat injected with calcium chloride or sodium chloride were evaluated. Hot-boned breast fillets were injected to 10% (wt/wt) with 0.3 M CaCl2 or 0.6 M NaCl, tumbled, and aged 24 h. Tumbling was conducted at 20 C, -635 mm Hg, 20 rpm for 1 h. Hot-boned and cold-boned (24 h) fillets were used as controls. One fillet from each carcass was baked and sheared with an Allo-Kramer cell, whereas the other fillet was used for biochemical analysis. Shear values indicated that both CaCl2- and NaCl-treated samples had significantly (P < 0.05) lower shear values than hot-boned controls but were similar (P > 0.05) to cold-boned samples. The CaCl2 injection treatment significantly elevated (P < 0.05) the tissue calcium content compared to all other treatments. There was no significant difference in heat-stable collagen content (P > 0.05) among all treatments, which indicated that CaCl2 or NaCl did not contribute to meat tenderness through degradative changes in collagen. Calpain data indicated that mu-calpain had disappeared by 24 h aging in all treatments. The m-calpain activity was significantly lower (P < 0.05) in samples treated with CaCl2 than in the other samples. The NaCl-treated samples had m-calpain activity similar (P > 0.05) to that of hot-boned controls. Sarcomeres of CaCl2-treated samples were significantly shorter (P < 0.05) than those of cold-boned controls, were similar (P > 0.05) to those of hot-boned controls, and were shorter than those of NaCl-treated muscles. The sarcomere length and calpain data suggest that CaCl2 tenderized fillets by ionic strength and calcium-specific effects (possibly a proteolytic action), whereas the NaCl solution tenderized by ionic strength effect at a similar conductivity level to that of the CaCl2 solution.
对注射氯化钙或氯化钠的废弃鸡肉的生化特性进行了评估。将热剔骨鸡胸肉片用0.3M氯化钙或0.6M氯化钠注射至10%(重量/重量),翻滚处理,并陈化24小时。翻滚处理在20℃、-635mmHg、20转/分钟的条件下进行1小时。热剔骨和冷剔骨(24小时)的肉片用作对照。从每个胴体中取一片肉片进行烘烤,并用Allo-Kramer剪切仪进行剪切,而另一片肉片用于生化分析。剪切值表明,氯化钙和氯化钠处理的样品的剪切值均显著低于热剔骨对照(P<0.05),但与冷剔骨样品相似(P>0.05)。与所有其他处理相比,氯化钙注射处理显著提高了组织钙含量(P<0.05)。所有处理之间的热稳定胶原蛋白含量没有显著差异(P>0.05),这表明氯化钙或氯化钠不会通过胶原蛋白的降解变化促进肉的嫩度。钙蛋白酶数据表明,在所有处理中,μ-钙蛋白酶在陈化24小时后消失。氯化钙处理的样品中的m-钙蛋白酶活性显著低于其他样品(P<0.05)。氯化钠处理的样品的m-钙蛋白酶活性与热剔骨对照相似(P>0.05)。氯化钙处理的样品的肌节明显短于冷剔骨对照(P<0.05),与热剔骨对照相似(P>0.05),且短于氯化钠处理肌肉的肌节。肌节长度和钙蛋白酶数据表明,氯化钙通过离子强度和钙特异性效应(可能是蛋白水解作用)使肉片嫩化,而氯化钠溶液在与氯化钙溶液相似的电导率水平下通过离子强度效应使肉片嫩化。