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[T4噬菌体DNA连接酶的寡脱氧核糖核苷酸的可控连接]

[Controlled ligation of oligodeoxyribonucleotides of DNA-ligase of the T4 phage].

作者信息

Koroleva O N, Drutsa V L

出版信息

Mol Biol (Mosk). 1988 Nov-Dec;22(6):1632-41.

PMID:3252153
Abstract

The enzymatic ligation of 5-10-membered synthetic oligodeoxyribonucleotides forming the complementary DNA-like duplexes has been studied. The possibility of selective DNA ligase catalyzed ligation of 5'-adenylylated derivatives of oligonucleotides in the absence of rATP and also the selective joining of cohesive ends in the presence of blunt ends in the complex mixtures of oligonucleotides at definite concentrations of rATP have been demonstrated. The influence of length and sequence of short synthetic DNA-duplexes on the efficiency of ligation has been shown. We have identified the unusual octanucleotide dpTATAATAT, that being able to form concatemer complexes could not be polymerized by T4 DNA ligase.

摘要

对形成互补DNA样双链体的5至10元合成寡脱氧核糖核苷酸的酶促连接进行了研究。已证明在不存在rATP的情况下,DNA连接酶可选择性催化寡核苷酸的5'-腺苷酸化衍生物的连接,并且在特定浓度的rATP下,在寡核苷酸的复杂混合物中存在平端时可选择性连接粘性末端。已表明短合成DNA双链体的长度和序列对连接效率的影响。我们鉴定出了不寻常的八核苷酸dpTATAATAT,它能够形成串联复合物,但不能被T4 DNA连接酶聚合。

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