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[利用某些标记酶对豚鼠肠平滑肌富含质膜部分的检测(作者译)]

[Examination of plasma membrane-enriched fraction from guinea pig intestinal smooth muscle by means of some marker enzymes (author's transl)].

作者信息

Yamamoto K, Yabu H

出版信息

Nihon Heikatsukin Gakkai Zasshi. 1979 Dec;15(4):337-51. doi: 10.1540/jsmr1965.15.337.

Abstract

By means of a preparation technique based on the discontinuous sucrose density gradient, subcellular fractions were isolated from guinea pig intestinal smooth muscle cells. A fraction which distributed to a 33% sucrose layer showed relatively high activities of 5'-nucleotidase, Na+ . K+-ATPase and ouabain sensitive Na+ . K+-ATPase. The fraction had a low NaN3 sensitive Mg2+-ATPase activity. On the other hand, the high activity of glucose-6-phosphatase showed a broad distribution. Though the sucrose density gradient proceeded over a series of the fine layers, cross-contamination of microsome into the 33% sucrose fraction was not reduced. To reduce microsomal cross-contamination, another procedure was employed. The homogenization time of 77000 xg sediment to be layered on the top of the sucrose density gradients was prolonged. This procedure did not change the distribution of K+ activated p-nitrophenylphosphatase, K+ activated ouabain sensitive p-nitrophenylphosphatase and ouabain sensitive Na+ . K+-ATPase activities. The peak of NADH cytochrome c reductase activity was shifted to a 38% sucrose fraction from a 33% sucrose fraction and the activity of this marker enzyme in the 33% sucrose fraction decreased to 60% of that of the prior procedure.

摘要

通过基于不连续蔗糖密度梯度的制备技术,从豚鼠肠道平滑肌细胞中分离出亚细胞组分。分布在33%蔗糖层的组分显示出相对较高的5'-核苷酸酶、Na⁺.K⁺-ATP酶和哇巴因敏感的Na⁺.K⁺-ATP酶活性。该组分的NaN₃敏感的Mg²⁺-ATP酶活性较低。另一方面,葡萄糖-6-磷酸酶的高活性呈现广泛分布。尽管蔗糖密度梯度经过一系列精细层,但微粒体向33%蔗糖组分的交叉污染并未减少。为减少微粒体交叉污染,采用了另一种方法。延长了要铺在蔗糖密度梯度顶部的77000×g沉淀物的匀浆时间。该方法并未改变K⁺激活的对硝基苯磷酸酶、K⁺激活的哇巴因敏感的对硝基苯磷酸酶和哇巴因敏感的Na⁺.K⁺-ATP酶活性的分布。NADH细胞色素c还原酶活性的峰值从33%蔗糖组分转移到了38%蔗糖组分,并且该标记酶在33%蔗糖组分中的活性降至先前方法的60%。

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