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Post-mortem activity of the glycogen debranching enzyme and change in the glycogen pools in porcine M. longissimus dorsi from carriers and non-carriers of the RN− gene

机译:猪背支背根线虫的RN-基因携带者和非携带者糖原解支酶的事后活性和糖原池的变化

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摘要

Glycogen debranching enzyme (GDE) is together with glycogen phosphorylase responsible for the degradation of glycogen. The present study compares the post-mortem activity of GDE and breakdown of the glycogen pools in M. longissimus dorsi of RN- carrier pigs and in wild type animals. The activity of GDE (n=14) and pH (n=20) was measured 0.5, 3, 5, 24 and 48 h post-mortem. The change in pro-glycogen and in macro-glycogen content (n=20) was followed until 216 h post-mortem and the transcription level of GDE, glycogenin and glycogen synthase m-RNA (n=19) were measured 0.5 h post-mortem. Both the activity of GDE and the transcription level of GDE were found to be similar in RN- carriers and wild type animals shortly after slaughter. However, the activity declined faster in wild type animals compared with RN- carriers with increasing time post-mortem. The contents of both pro-glycogen and macro-glycogen were higher in RN- carriers compared with wild type animals, and further, the proportion of macro-glycogen was higher in RN- carriers compared with wild type animals. During the post-mortem period, only degradation of pro-glycogen was observed in both genotypes. The decrease in pH was faster and the ultimate pH lower in RN- carriers than in wild type animals. It was suggested that the higher GDE activity in the late phase of the post-mortem period in muscles from RN- carriers renders the extended pH decrease in these muscles.
机译:糖原解支酶(GDE)与糖原磷酸化酶一起负责糖原的降解。本研究比较了带有RN的猪的长背支原体背阔肌和野生型动物中GDE的事后活性和糖原池的分解。在死后0.5、3、5、24和48小时测量GDE的活性(n = 14)和pH(n = 20)。追踪促糖原和大糖原含量(n = 20)的变化,直到死后216 h,并在转染后0.5 h测量GDE,糖原蛋白和糖原合酶m-RNA(n = 19)的转录水平。验尸。屠宰后不久,在RN携带者和野生型动物中发现GDE的活性和GDE的转录水平相似。但是,与死后的时间相比,与RN携带者相比,野生型动物的活性下降得更快。与野生型动物相比,RN-载体中原糖原和大糖原的含量均较高,此外,RN-载体中大糖原的比例也较高。在死后期间,两种基因型仅观察到原糖原降解。与野生型动物相比,RN携带者的pH降低更快,最终pH更低。有人提出,在死后后期,RN携带者的肌肉中较高的GDE活性使这些肌肉的pH值持续下降。

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