死后早期蛋白质组和代谢组对最终pH值和猪肉品质的贡献

E. Zuber, Amanda C. Outhouse, E. Helm, N. Gabler, K. Prusa, E. Steadham, E. Huff-Lonergan, S. Lonergan
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引用次数: 4

摘要

本研究的目的是确定最终pH值的细微差异与猪肉质量的差异之间的关系,并了解死后早期糖酵解如何导致最终pH值的变化。假设死后早期胸腰最长肌蛋白质组和代谢组中的元素可用于预测与pH值下降相关的质量缺陷。分别于死后45 min、24 h和14 d测量胸腰最长肌的温度和pH值。陈化14 d后进行质量测量。各组分为正常pH (NpH;X ' = 5。59 (5.53 - -5.67);NpH, n = 10)和低pH (LpH;X ' = 5。42 (5.38 - -5.45);死后14 d LpH, n = 10)。用GC-MS鉴定死后45分钟的代谢物。用凝胶电泳的二维差异定量蛋白质之间的相对差异,用MALDI-MS鉴定斑点。Western blot分析在死后45分钟和14天检测磷酸果糖激酶、过氧化物还原素-2和还原和非还原的腺苷单磷酸脱氨酶-2。最终pH分型不影响死后45 min pH值(P = 0.64);14 d pH组间差异有统计学意义(P < 0.01)。NpH的吹扫损失较小(P < 0.01),颜色较深(P < 0.01),星探较低(P < 0.01),第7天的完整desmin较少(P = 0.02)。NpH组丙酮酸增加(P = 0.01),乳酸减少(P = 0.09),可溶性乳酸脱氢酶增加(P = 0.03),丙酮酸激酶增加(P < 0.10)。这些观察结果表明,酶丰度或溶解度的差异可能产生更多的丙酮酸和更少的乳酸。果糖6-磷酸在LpH组更丰富(P = 0.08),表明磷酸果糖激酶可能参与糖酵解差异。此外,死后早期的热休克蛋白、过氧化物还原素-2 (P = 0.02)和苹果酸盐(P = 0.01)丰度更高,都表明线粒体功能和氧化稳定性的差异导致了质量差异。这些结果表明,即使是最终pH值的细微变化也会影响猪肉的品质。死后45分钟的蛋白质组和代谢组与pH下降程度的变化有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contribution of Early-Postmortem Proteome and Metabolome to Ultimate pH and Pork Quality
This study's objectives were to identify how subtle differences in ultimate pH relate to differences in pork quality and to understand how early-postmortem glycolysis contributes to variation in ultimate pH. The hypothesis was that elements in early-postmortem longissimus thoracis et lumborum proteome and metabolome could be used to predict quality defects associated with pH decline. Temperature and pH of the longissimus thoracis et lumborum were measured at 45 min, 24 h, and 14 d postmortem. Quality measurements were made after 14 d of aging. Groups were classified as normal pH (NpH; x̄ = 5 . 59 [5.53–5.67]; NpH, n = 10) and low pH (LpH; x̄ = 5 . 42 [5.38–5.45]; LpH, n = 10) at 14 d postmortem. Metabolites from 45 min postmortem were identified using GC-MS. Relative differences between proteins were quantified with two-dimensional difference in gel electrophoreses, and spots were identified with MALDI-MS. Western blot analyses were used to measure phosphofructokinase, peroxiredoxin-2, and reduced and non-reduced adenosine monophosphate deaminase-2 at 45 min and 14 d postmortem. Ultimate pH classification did not affect 45-min-postmortem pH (P = 0.64); 14-d pH was different between groups (P < 0.01). NpH had less purge loss (P < 0.01), was darker (P < 0.01), had lower star probe (P < 0.01), and had less intact day-7 desmin (P = 0.02). More pyruvate (P = 0.01) and less lactate (P = 0.09) was observed in NpH, along with more soluble lactate dehydrogenase (P = 0.03) and pyruvate kinase (P < 0.10). These observations indicate that differences in enzyme abundance or solubility may produce more pyruvate and less lactate. Fructose 6-phosphate was more abundant (P = 0.08) in the LpH group, indicating that phosphofructokinase may be involved in glycolytic differences. Furthermore, greater abundance of heat shock proteins, peroxiredoxin-2 (P = 0.02), and malate (P = 0.01) early postmortem all suggest differences in mitochondrial function and oxidative stability that contribute to quality differences. These results show that even subtle changes in ultimate pH can influence pork quality. The proteome and metabolome at 45 min postmortem are associated with variation in the extent of pH decline.
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