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首页> 外文期刊>The Journal of Experimental Biology >Osmotic effects on arginine kinase function in living muscle of the blue crab Callinectes sapidus
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Osmotic effects on arginine kinase function in living muscle of the blue crab Callinectes sapidus

机译:渗透对蓝蟹Callinectes sapidus活肌中精氨酸激酶功能的影响

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Flux was examined through the reaction catalyzed by arginine kinase in intact blue crab (Callinectes sapidus) muscle during simulated changes in salinity. Isolated dark Ievator muscles from the swimming leg were superfused with a saline solution that had an osmolarity equivalent to that of the hemolymph under different salinity regimes. Animals were acclimated for 7 days to a salinity of 5, 17 or 35parts per thousand, which corresponds to a hemolymph osmolarity of 640, 720 or 960 mosmol l(-1), respectively. Experiments were conducted under control conditions, in which the osmolarity of the superfusion medium matched that of the acclimated hemolymph, as well as under hypo- and hyperosmotic conditions. These latter treatments were meant to simulate a rapid change in environmental salinity. Pseudo-first-order unidirectional rate constants and flux rates were measured for arginine kinase in the forward and reverse directions using a P-31-nuclear magnetic resonance saturation transfer method. There were no differences in the rate constants or flux rates among the controls, indicating that arginine kinase function is not modulated by salinity if the animal has had sufficient acclimation time. However, the rate constants and flux rates of arginine kinase varied over a modest 1.7-fold range across the three types of osmotic treatments, although the range for the flux data was reduced when cell volume changes were taken into account. The hyperosmotic treatments led to a reduction in arginine kinase flux, while the hypo-osmotic treatments led to an enhanced arginine kinase flux. We propose that this effect is mediated by an increase in the concentration of perturbing inorganic ions under hyperosmotic conditions and a decrease in the concentration of such ions during the hypo-osmotic treatments.
机译:通过在盐度模拟变化期间完整蓝蟹(Callinectes sapidus)肌肉中精氨酸激酶催化的反应检查通量。在盐度不同的情况下,将从游泳腿分离出的深色Ievator肌肉与盐溶液融合,该溶液的渗透压与血淋巴的渗透压相同。使动物适应7天的盐度为千分之5、17或35份,这分别对应于640、720或960 mosmol l(-1)的血淋巴渗透压。在对照条件下进行实验,在该条件下,超融合培养基的渗透压与适应的血淋巴的渗透压相同,并且在低渗和高渗条件下。后面的这些处理旨在模拟环境盐度的快速变化。使用P-31核磁共振饱和转移方法在向前和向后方向测量精氨酸激酶的伪一阶单向速率常数和通量速率。对照之间的速率常数或通量速率没有差异,表明如果动物具有足够的适应时间,则精氨酸激酶功能不受盐度的调节。然而,虽然考虑到细胞体积的变化,通量数据的范围有所缩小,但在三种类型的渗透处理中,精氨酸激酶的速率常数和通量速率在1.7倍的适度范围内变化。高渗处理导致精氨酸激酶通量减少,而低渗处理导致精氨酸激酶通量增加。我们提出,这种影响是由高渗条件下扰动的无机离子浓度的增加和低渗处理过程中这类离子浓度的降低所介导的。

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