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Calcium plays a signiﬁcant role in the living muscle, causing contraction and relaxation. Most of the calcium in the cell is contained in the sarcoplasmic reticulum (SR). Mitochondria are secondary calcium‐sequestering organelles. After death, calcium seeps from the SR and activates an enzyme system called calpains. Calpains work to degrade muscle proteins and results in higher tenderness. Therefore, calcium ﬂux impacts tenderness.
Research from this lab has found that beef from cattle fed distillers grains is often more tender than cattle fed corn. However, the mechanism for the diﬀerence in tenderness has not yet been identiﬁed. It is well known that feeding distillers grains increases polyunsaturated fatty acid (PUFA) content in the muscle, and recently this lab demonstrated that feeding distillers grains increases PUFA of the SR itself.
The hypothesis is that PUFA content in the SR membrane would increase as a consequence of feeding distiller’s grains, which would predispose the SR membrane to oxidation, and cause a greater postmortem release of calcium into the cytoplasm. Cytoplasmic calcium would activate proteolytic degradation via the calpain system and thereby enhance tenderness.
It is hard to measure calcium release within the cell because calcium binds with many diﬀerent proteins, making it diﬃcult to quantify how much has been released. The best approach is to isolate an organelle containing calcium and quantify calcium release under various conditions. Isolating intact SR proves very challenging, however. The structure of the sleeve‐like organelle makes it exceptionally diﬃcult to isolate without damaging its inherent structure. Fortunately, mitochondria are relatively easy to isolate intact and oﬀer the opportunity to study calcium release from an organelle under carefully controlled and tightly deﬁned conditions. In this way, mitochondria can be used as a model system for the SR in the study of calcium ﬂux.
The goal of this research was to 1) Help decipher the mechanism by which beef cattle fed distillers grains becomes more tender than beef ﬁnished on corn, with an overall goal of improving beef tenderness; 2) Determine the eﬀects of diet (corn vs distillers grain) on fatty acid composition of the membranes of the SR and mitochondria; 3) Evaluate the eﬀects of membrane fatty acid composition (PUFA content) on calcium release; 4) Determine the inﬂuence of oxidation on calcium release; and 5) Relate fatty acid composition of the whole muscle to fatty acid composition of the SR and mitochondrial membranes.
This study found that oxidation decreases the ability of the mitochondria to retain calcium; more PUFA were found in the SR and mitochondria from cattle fed distillers grains; and, mitochondria from cattle fed distillers grains tended to retain less calcium than mitochondria from cattle fed corn‐only.
In both the SR and the mitochondria, the distillers grain diet had a higher amount of PUFA compared to corn samples. Day 14 mitochondria had higher PUFA compared to day two and eight mitochondria, as expected from aging of unsaturated fats. Phospholipid content of the mitochondria and SR were unaﬀected by diet. Oxidized mitochondria retained less Ca than non‐oxidized mitochondria. Day two mitochondria retained less Ca than day eight mitochondria. Overall, mitochondria from cattle ﬁnished on corn tended to retain more Ca than mitochondria from cattle ﬁnished on DG.
Results indicate that greater PUFA content deposited in organelles may aﬀect Ca ﬂux by increased susceptibility to oxidation. A distiller’s grain diet may inﬂuence Ca ﬂux and ultimate tenderness by this mechanism.
Tenderness is one of the most important attributes of a consumer’s eating experience and inﬂuences the economic value of beef. Diets, such as distillers’ grains, have the opportunity to impact the ultimate tenderness of beef. Better understanding of the biology of beef tenderization and how to alter beef tenderness can provide for the development of strategies to optimize tenderness and achieve the highest possible value for beef and consumer satisfaction ratings.
Figure 1. Emery working with mitochondria.
Figure 2. Nicholas working on protein.
Figure 1. Effects of oxidation on mitochondrial calcium retention.
Figure 2. Diet effect on mitochondrial calcium retention.