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两种小麦胚蛋白磷酸酶的纯化与特性分析

Purification and characterization of two wheat-embryo protein phosphatases.

作者信息

Polya G M, Haritou M

机构信息

Department of Biochemistry, La Trobe University, Bundoora, Victoria, Australia.

出版信息

Biochem J. 1988 Apr 15;251(2):357-63. doi: 10.1042/bj2510357.

Abstract

Two protein phosphatases (enzymes I and II) were extensively purified from wheat embryo by a procedure involving chromatography on DEAE-cellulose, phenyl-Sepharose CL-4B, DEAE-Sephacel and Ultrogel AcA 44. Preparations of enzyme I (Mr 197,000) are heterogeneous. Preparations of enzyme II (Mr 35,000) contain only one major polypeptide (Mr 17,500), which exactly co-purifies with protein phosphatase II on gel filtration and is not present in preparations of enzyme I. However, this major polypeptide has been identified as calmodulin. Calmodulin and protein phosphatase II can be separated by further chromatography on phenyl-Sepharose CL-4B. Protein phosphatases I and II do not require Mg2+ or Ca2+ for activity. Both enzymes catalyse the dephosphorylation of phosphohistone H1 (phosphorylated by wheat-germ Ca2+-dependent protein kinase) and of phosphocasein (phosphorylated by wheat-germ Ca2+-independent casein kinase), but neither enzyme dephosphorylates a range of non-protein phosphomonoesters tested. Both enzymes are inhibited by Zn2+, Hg2+, vanadate, molybdate, F-, pyrophosphate and ATP.

摘要

通过在DEAE - 纤维素、苯基 - 琼脂糖CL - 4B、DEAE - 琼脂糖凝胶和Ultrogel AcA 44上进行色谱分析的方法,从小麦胚中大量纯化了两种蛋白磷酸酶(酶I和酶II)。酶I(分子量197,000)的制剂具有异质性。酶II(分子量35,000)的制剂仅含有一种主要多肽(分子量17,500),该多肽在凝胶过滤时与蛋白磷酸酶II完全共纯化,且不存在于酶I的制剂中。然而,这种主要多肽已被鉴定为钙调蛋白。钙调蛋白和蛋白磷酸酶II可通过在苯基 - 琼脂糖CL - 4B上进一步色谱分析分离。蛋白磷酸酶I和II的活性不需要Mg2+或Ca2+。两种酶都催化磷酸组蛋白H1(由小麦胚Ca2+依赖性蛋白激酶磷酸化)和磷酸酪蛋白(由小麦胚Ca2+非依赖性酪蛋白激酶磷酸化)的去磷酸化,但两种酶都不能使一系列测试的非蛋白磷酸单酯去磷酸化。两种酶都受到Zn2+、Hg2+、钒酸盐钼酸盐、F - 、焦磷酸盐和ATP的抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e7b/1149010/c63bef32cdc2/biochemj00233-0055-a.jpg

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