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在牛肉死后老化过程中,主要的 110 和 30 kDa 蛋白水解片段的出现程度和速度取决于肌肉的糖酵解速度和老化时间:一种通过 LC-MS/MS 解析其蛋白质组及其相关途径的方法。

The Extent and Rate of the Appearance of the Major 110 and 30 kDa Proteolytic Fragments during Post-Mortem Aging of Beef Depend on the Glycolysing Rate of the Muscle and Aging Time: An LC-MS/MS Approach to Decipher Their Proteome and Associated Pathways.

机构信息

Food Quality and Sensory Science Department, Teagasc Ashtown Food Research Centre, Ashtown, Dublin 15, Ireland.

出版信息

J Agric Food Chem. 2021 Jan 13;69(1):602-614. doi: 10.1021/acs.jafc.0c06485. Epub 2020 Dec 30.

Abstract

Post-mortem (p-m) muscle undergoes a myriad of complex physical and biochemical changes prior to its conversion to meat, which are influential on proteolysis and hence tenderization. A more in-depth understanding of the mechanisms underpinning these dynamics is a key to consistently providing tender beef. Using an LC-MS/MS approach, with state-of-art mass spectrometry Q Exactive HF-X, the proteome and associated pathways contributing to the appearance of the proteolytic breakdown products appearing over 14 days p-m, at two important molecular weights (110 and 30 kDa) on 1D SDS-PAGE gels, have been investigated in beef muscles exhibiting four rates of pH decline differentiated on the basis of time at pH 6 (fast glycolysing, <3 h; medium, 3-5 h; slow, 5-8 h; and very slow, 8+ h). Both 110 and 30 kDa bands appeared during aging and increased in intensity as a function of p-m time in a pH decline-dependent manner. The 110 kDa band appeared as early as 3 h p-m and displayed an incremental increase in all groups through to 14 days p-m. From 2 days p-m, this increase in abundance during aging was significantly ( < 0.001) influenced by the glycolytic rate: fast > or = medium > slow > very slow. The day 2 p-m appearance of the 30 kDa band was most evident for the fast glycolysing muscle with little or no evidence of appearance in slow and very slow. For days 7 and 14 p-m, the strength of appearance was dependent on glycolysing groups fast > medium > or = slow > very slow. LC-MS/MS analysis yielded a total of 22 unique proteins for the 110 kDa fragment and 13 for the 30 kDa, with 4 common proteins related to both the actin and fibrinogen complex. The Gene Ontology analysis revealed that a myriad of biological pathways are influential with many related to proteins involved primarily in muscle contraction and structure. Other pathways of interest include energy metabolism, apoptotic mitochondrial changes, calcium and ion transport, and so on. Interestingly, most of the proteins composing the fragments were so far identified as biomarkers of beef tenderness and other quality traits.

摘要

死后(p-m)肌肉在转化为肉之前会经历一系列复杂的物理和生化变化,这些变化会影响蛋白质的水解,从而影响肉的嫩度。深入了解这些动态变化的机制是始终提供嫩牛肉的关键。本研究使用基于液相色谱-串联质谱(LC-MS/MS)的方法,结合最先进的质谱 Q Exactive HF-X,研究了在牛肉肌肉中,在两个重要的分子量(110 kDa 和 30 kDa)上的 1D SDS-PAGE 凝胶上,出现于死后 14 天的蛋白质水解产物的出现与哪些蛋白质及相关途径有关,这些变化与四种基于 pH6 时的 pH 值下降速率(快速糖酵解,<3 h;中速,3-5 h;慢速,5-8 h;非常慢速,8+ h)相关。110 kDa 和 30 kDa 条带在老化过程中出现,并随着 pH 值下降时间的延长而增加,呈 pH 值依赖性。110 kDa 条带早在死后 3 h 时出现,并在所有组中随着死后时间的延长而逐渐增加。从 2 天 p-m 开始,这种随着老化而增加的丰度显著( < 0.001)受到糖酵解速率的影响:快速 > = 中速 > 慢速 > 非常慢速。在快速糖酵解肌肉中,30 kDa 条带在死后 2 天的出现最为明显,在慢速和非常慢速肌肉中几乎没有或没有出现的迹象。对于死后 7 天和 14 天,条带的出现强度取决于糖酵解组:快速 > 中速 > = 慢速 > 非常慢速。LC-MS/MS 分析共获得了 110 kDa 片段的 22 种独特蛋白质和 30 kDa 片段的 13 种独特蛋白质,其中 4 种与肌动蛋白和纤维蛋白原复合物相关的共同蛋白质。GO 分析表明,许多生物学途径都具有重要影响,其中许多与主要参与肌肉收缩和结构的蛋白质有关。其他感兴趣的途径包括能量代谢、凋亡线粒体变化、钙和离子转运等。有趣的是,构成片段的大多数蛋白质迄今为止被鉴定为牛肉嫩度和其他质量性状的生物标志物。

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