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豌豆DNA甲基化酶的DNA底物特异性

DNA substrate specificity of pea DNA methylase.

作者信息

Houlston C E, Cummings M, Lindsay H, Pradhan S, Adams R L

机构信息

Department of Biochemistry, University of Glasgow, U.K.

出版信息

Biochem J. 1993 Aug 1;293 ( Pt 3)(Pt 3):617-24. doi: 10.1042/bj2930617.

Abstract

DNA methylase, present in low-salt extracts of nuclei prepared from Pisum sativum shoot tips, methylates model DNA substrates containing CNG trinucleotides or CI dinucleotides only. The binding to the hemimethylated trinucleotide substrates is very much stronger and more persistent than the binding to the unmethylated substrates or to the hemimethylated dinucleotide substrate. When the DNA concentration is limiting, the rate of methyl-group transfer with the hemimethylated CNG substrate is much greater than that with the unmethylated CNG. However, the Vmax. is similar for the two CNG substrates. On fractionation using Q-Sepharose, two peaks of activity are seen with different relative activities using the di- and trinucleotide substrates. The relative activity with these substrates changes during purification, during plant growth and on heating at 35 degrees C as well, indicating that more than one enzyme or more than one form of the enzyme may be present.

摘要

从豌豆幼苗顶端制备的细胞核低盐提取物中存在的DNA甲基化酶,仅使含有CNG三核苷酸或CI二核苷酸的模型DNA底物发生甲基化。与半甲基化三核苷酸底物的结合比与未甲基化底物或半甲基化二核苷酸底物的结合要强得多且更持久。当DNA浓度受到限制时,半甲基化CNG底物的甲基基团转移速率远高于未甲基化CNG底物。然而,两种CNG底物的最大反应速度相似。使用Q-琼脂糖进行分级分离时,会出现两个活性峰,使用二核苷酸和三核苷酸底物时相对活性不同。这些底物的相对活性在纯化过程中、植物生长过程中以及在35℃加热时也会发生变化,这表明可能存在不止一种酶或不止一种酶形式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/116d/1134411/9d45335aad1d/biochemj00106-0028-a.jpg

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