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[生态大坝DNA甲基化酶对单链序列和合成寡核苷酸的影响]

[Effect of Ecodam DNA-methylase on single-stranded sequences and synthetic oligonucleotides].

作者信息

Zinov'ev V V, Gorbunov Iu A, Popov S G, Malygin E G, Bur'ianov Ia I

出版信息

Mol Biol (Mosk). 1985 Jul-Aug;19(4):947-54.

PMID:3900694
Abstract

Interaction of the Ecodam methylase with different substrates were investigated among them the double- and single-stranded DNAs and synthetic oligonucleotides containing some defects in the GATC sequence. These defects were:nick, the absence of one internucleotide phosphate of nucleotide; partially single-stranded form on the recognition site etc. It was demonstrated that the presence of both G . A-dinucleotides in the recognition site is necessary for productive enzyme-substrate interaction. The absence of T and/or C residues is less dramatic for methylase activity. The Ecodam methylase is capable to modify the single-stranded oligonucleotides by forming the double-stranded structure in the symmetric recognition sequences GATC.

摘要

研究了Ecodam甲基化酶与不同底物的相互作用,其中包括双链和单链DNA以及在GATC序列中存在一些缺陷的合成寡核苷酸。这些缺陷包括:缺口,即核苷酸中一个核苷酸间磷酸缺失;识别位点上的部分单链形式等。结果表明,识别位点中同时存在G.A二核苷酸对于有效的酶-底物相互作用是必要的。T和/或C残基的缺失对甲基化酶活性的影响较小。Ecodam甲基化酶能够通过在对称识别序列GATC中形成双链结构来修饰单链寡核苷酸。

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