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酵母液泡中精氨酸特异性转运系统的特性研究

Characterization of a specific transport system for arginine in isolated yeast vacuoles.

作者信息

Boller T, Dürr M, Wiemken A

出版信息

Eur J Biochem. 1975 May;54(1):81-91. doi: 10.1111/j.1432-1033.1975.tb04116.x.

Abstract

The transport of L-arginine was studied in isolated vacuoles of Saccharomyces cerevisiae. A centrifugation method allowed rapid separation of the fragile vacuoles from the incubation media so that initial uptake rates of [14C]arginine could be measured. Labelled arginine added to the medium was accumulated in the isolated vacuoles; it was found to exchange specifically with the arginine already present in the vacuoles. Such an exchange did not take place in intact spheroplasts. The pH dependence of the arginine transport in the vacuoles was tested. As the vacuoles are unstable in the pH range of optimal transport activity (pH above 7.0), the pH optimum of the transport reaction could not be determined. From the temperature dependence, the apparent energy of activation was calculated to be 9800 cal/mol. Arginine transport shows saturation kinetics with an apparent Km of 30 muM in the isolated vacuoles, and of 1.5 muM in the spheroplasts. Competition experiments with amino acids and arginine analogues demonstrated that the arginine transport in both vacuoles and spheroplasts, is highly specific. The two systems, however, were shown to have distinct specificities. The inhibition of vacuolar L-arginine transport by D-arginine, L-histidine, and L-canavanine was competitive with apparent Ki values of 60 muM, 400 muM and 600 muM respectively.

摘要

在酿酒酵母的分离液泡中研究了L-精氨酸的转运。一种离心方法能使脆弱的液泡快速从孵育培养基中分离出来,从而可以测量[14C]精氨酸的初始摄取速率。添加到培养基中的标记精氨酸在分离的液泡中积累;发现它能与液泡中已有的精氨酸特异性交换。这种交换在完整的原生质球中不会发生。测试了液泡中精氨酸转运的pH依赖性。由于液泡在最佳转运活性的pH范围内(pH高于7.0)不稳定,因此无法确定转运反应的最适pH。根据温度依赖性计算出表观活化能为9800卡/摩尔。精氨酸转运在分离的液泡中呈现饱和动力学,表观Km为30μM,在原生质球中为1.5μM。用氨基酸和精氨酸类似物进行的竞争实验表明,液泡和原生质球中的精氨酸转运具有高度特异性。然而,这两个系统显示出不同的特异性。D-精氨酸、L-组氨酸和L-刀豆氨酸对液泡L-精氨酸转运的抑制是竞争性的,表观Ki值分别为60μM、400μM和600μM。

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