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影响高活性谷胱甘肽转移酶功能比较的实验条件。

Experimental conditions affecting functional comparison of highly active glutathione transferases.

机构信息

Department of Biochemistry and Organic Chemistry, Uppsala University, SE-75123 Uppsala, Sweden.

出版信息

Anal Biochem. 2011 Jun 1;413(1):16-23. doi: 10.1016/j.ab.2011.01.041. Epub 2011 Feb 2.

Abstract

Glutathione transferases (GSTs, EC 2.5.1.18) possess multiple functions and have potential applications in biotechnology. Direct evidence of underestimation of activity of human GST A3-3 and porcine GST A2-2 measured at submicromolar enzyme concentrations is reported here for the first time. The combination of time-dependent and enzyme concentration-dependent loss of activity and the choice of the organic solvent for substrates were found to cause irreproducibility of activity measurements of GSTs. These effects contribute to high variability of activity values of porcine GST A2-2 and human Alpha-class GSTs reported in the literature. Adsorption of GSTs to surfaces was found to be the main explanation of the observed phenomena. Several approaches to improved functional comparison of highly active GSTs are proposed.

摘要

谷胱甘肽转移酶(GSTs,EC 2.5.1.18)具有多种功能,在生物技术中有潜在的应用。本文首次报道了在亚毫摩尔酶浓度下,人 GST A3-3 和猪 GST A2-2 的活性被低估的直接证据。研究发现,活性的时间依赖性和酶浓度依赖性丧失以及对底物有机溶剂的选择导致 GST 活性测量的不可重复性。这些效应导致文献中报道的猪 GST A2-2 和人 Alpha 类 GSTs 的活性值具有高度可变性。研究发现 GSTs 吸附到表面是观察到的现象的主要原因。本文提出了几种改进高度活跃的 GSTs 功能比较的方法。

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