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对一种夏眠陆地蜗牛足部肌肉中谷氨酸脱氢酶的体内调节机制的深入了解。

Insights into the in vivo regulation of glutamate dehydrogenase from the foot muscle of an estivating land snail.

作者信息

Bell Ryan A V, Dawson Neal J, Storey Kenneth B

机构信息

Department of Chemistry, Carleton University, 1125 Colonel By Drive, Ottawa, ON, Canada K1S 5B6.

出版信息

Enzyme Res. 2012;2012:317314. doi: 10.1155/2012/317314. Epub 2012 Mar 26.

Abstract

Land snails, Otala lactea, survive in seasonally hot and dry environments by entering a state of aerobic torpor called estivation. During estivation, snails must prevent excessive dehydration and reorganize metabolic fuel use so as to endure prolonged periods without food. Glutamate dehydrogenase (GDH) was hypothesized to play a key role during estivation as it shuttles amino acid carbon skeletons into the Krebs cycle for energy production and is very important to urea biosynthesis (a key molecule used for water retention). Analysis of purified foot muscle GDH from control and estivating conditions revealed that estivated GDH was approximately 3-fold more active in catalyzing glutamate deamination as compared to control. This kinetic difference appears to be regulated by reversible protein phosphorylation, as indicated by ProQ Diamond phosphoprotein staining and incubations that stimulate endogenous protein kinases and phosphatases. The increased activity of the high-phosphate form of GDH seen in the estivating land snail foot muscle correlates well with the increased use of amino acids for energy and increased synthesis of urea for water retention during prolonged estivation.

摘要

陆地蜗牛,即乳白奥塔蜗牛,通过进入一种名为夏眠的需氧蛰伏状态,在季节性炎热干燥的环境中生存。在夏眠期间,蜗牛必须防止过度脱水,并重新组织代谢燃料的使用,以便在没有食物的情况下忍受较长时间。谷氨酸脱氢酶(GDH)被认为在夏眠过程中起关键作用,因为它将氨基酸碳骨架穿梭进入三羧酸循环以产生能量,并且对尿素生物合成(一种用于保水的关键分子)非常重要。对来自对照和夏眠条件下纯化的足部肌肉GDH的分析表明,与对照相比,夏眠状态下的GDH在催化谷氨酸脱氨方面的活性大约高3倍。如ProQ Diamond磷蛋白染色以及刺激内源性蛋白激酶和磷酸酶的孵育实验所示,这种动力学差异似乎受可逆性蛋白质磷酸化调节。在夏眠的陆地蜗牛足部肌肉中观察到的高磷酸化形式的GDH活性增加,与在长时间夏眠期间氨基酸用于能量的增加以及用于保水的尿素合成增加密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c6/3318891/b71747793075/ER2012-317314.001.jpg

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