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嘌呤碱基的酶促转糖基化作用。

An enzymatic transglycosylation of purine bases.

作者信息

Roivainen Jarkko, Elizarova Tatiana, Lapinjoki Seppo, Mikhailopulo Igor A, Esipov Roman S, Miroshnikov Anatoly I

机构信息

Department of Pharmaceutical Chemistry, University of Kuopio, Kuopio, Finland.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2007;26(8-9):905-9. doi: 10.1080/15257770701506343.

Abstract

An enzymatic transglycosylation of purine heterocyclic bases employing readily available natural nucleosides or sugar-modified nucleosides as donors of the pentofuranose fragment and recombinant nucleoside phosphorylases as biocatalysts has been investigated. An efficient enzymatic method is suggested for the synthesis of purine nucleosides containing diverse substituents at the C6 and C2 carbon atoms. The glycosylation of N(6)-benzoyladenine and N(2)-acetylguanine and its O(6)-derivatives is not accompanied by deacylation of bases.

摘要

研究了一种酶促转糖基化反应,该反应利用易于获得的天然核苷或糖修饰核苷作为戊呋喃糖片段的供体,并使用重组核苷磷酸化酶作为生物催化剂,对嘌呤杂环碱基进行转糖基化。提出了一种高效的酶促方法,用于合成在C6和C2碳原子上含有不同取代基的嘌呤核苷。N(6)-苯甲酰腺嘌呤和N(2)-乙酰鸟嘌呤及其O(6)-衍生物的糖基化反应不会伴随着碱基的脱酰基作用。

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