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过氧化物还原酶6——牛胸最长肌嫩度的潜在蛋白质标志物。

Peroxiredoxin-6--a potential protein marker for meat tenderness in bovine longissimus thoracis muscle.

作者信息

Jia X, Veiseth-Kent E, Grove H, Kuziora P, Aass L, Hildrum K I, Hollung K

机构信息

Nofima Mat AS, Osloveien 1, As, Norway.

出版信息

J Anim Sci. 2009 Jul;87(7):2391-9. doi: 10.2527/jas.2009-1792. Epub 2009 Apr 9.

Abstract

The muscle sarcoplasmic proteins from bovine M. longissimus thoracis muscle were studied using proteomics to identify possible protein markers for meat tenderness. This study included 3 experiments: A1, A2, and B. From a collection of biopsies from the bovine M. longissimus thoracis muscle, excised 4 d before slaughter from 178 Norwegian Red young bulls, 26 biopsies were studied in Exp. A1. Based on Warner-Bratzler shear force (WBSF) values at 7 d postmortem, the biopsies were separated into a tender and a tough group of 13 bulls each and analyzed by 2-dimensional gel electrophoresis (2-DE) and Western blotting. The 2-DE experiments identified 4 different proteins: stress-70 protein, protein DJ-1, peroxiredoxin-6, and malate dehydrogenase, which were different in abundance in the tender and tough groups. However, only peroxiredoxin-6 was confirmed by quantification from Western blots. Peroxiredoxin-6 is an antioxidant enzyme that plays a role in protecting cells from oxidative stress. Peroxiredoxin-6 was identified through 3 spots of the same molecular weight, but with different pI on the Western blots. Only one of the spots was more abundant in the biopsies from the tender group. In Exp. A2, samples collected 1 h postmortem from the same animals and muscles as in Exp. A1 were analyzed by Western blotting. In these postmortem samples, the same spot from peroxiredoxin-6 as in Exp. A1 was more abundant in the tender group. In addition, one of the other peroxiredoxin-6 spots was also more abundant in the tender group. To verify the results from Exp. A, biopsies from 14 additional animals were analyzed in Exp. B by Western blotting against stress-70 protein, protein DJ-1, peroxiredoxin-6, and malate dehydrogenase. No significant differences between the tough and tender groups could be observed in these biopsies. However, for peroxiredoxin-6, the tendencies pointed in the same direction as in Exp. A. In conclusion, peroxiredoxin-6 might be a potential protein marker for meat tenderness detectable in biopsies and in samples collected shortly after slaughter. However, more animals are needed to verify the findings in the present study.

摘要

利用蛋白质组学研究了来自牛胸最长肌的肌肉肌浆蛋白,以确定可能的肉质嫩度蛋白质标志物。本研究包括3个实验:A1、A2和B。从178头挪威红牛屠宰前4天切除的胸最长肌活检样本中,选取26个活检样本用于实验A1。根据死后7天的沃纳-布拉茨勒剪切力(WBSF)值,将活检样本分为嫩度组和韧性组,每组各13头公牛,并通过二维凝胶电泳(2-DE)和蛋白质免疫印迹法进行分析。2-DE实验鉴定出4种不同的蛋白质:应激70蛋白、DJ-1蛋白、过氧化物酶体增殖物激活受体6和苹果酸脱氢酶,它们在嫩度组和韧性组中的丰度不同。然而,通过蛋白质免疫印迹法定量仅证实了过氧化物酶体增殖物激活受体6。过氧化物酶体增殖物激活受体6是一种抗氧化酶,在保护细胞免受氧化应激方面发挥作用。过氧化物酶体增殖物激活受体6通过蛋白质免疫印迹法上3个分子量相同但pI不同的斑点鉴定出来。只有其中一个斑点在嫩度组的活检样本中更为丰富。在实验A2中,对与实验A1相同动物和肌肉在死后1小时采集的样本进行蛋白质免疫印迹分析。在这些死后样本中,与实验A1中过氧化物酶体增殖物激活受体6相同的斑点在嫩度组中更为丰富。此外,过氧化物酶体增殖物激活受体6的另一个斑点在嫩度组中也更为丰富。为了验证实验A的结果,在实验B中通过针对应激70蛋白、DJ-1蛋白、过氧化物酶体增殖物激活受体6和苹果酸脱氢酶的蛋白质免疫印迹法对另外14只动物的活检样本进行了分析。在这些活检样本中,未观察到韧性组和嫩度组之间有显著差异。然而,对于过氧化物酶体增殖物激活受体6,趋势与实验A相同。总之,过氧化物酶体增殖物激活受体6可能是一种潜在的肉质嫩度蛋白质标志物,可在活检样本和屠宰后不久采集的样本中检测到。然而,需要更多的动物来验证本研究的结果。

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