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[噬菌体T4的RNA连接酶。 IV. 十五聚核糖核苷酸ApUpG(pU)6(pA)5pAp的合成]

[RNA-ligase of bacteriophage T4. IV. Synthesis of pentadecaribonucleotide ApUpG(pU)6(pA)5pAp].

作者信息

Antsiferova V V, Ven'iaminova A G, Repkova M N, Iamkovoĭ V I

出版信息

Bioorg Khim. 1987 Aug;13(8):1031-6.

PMID:3675646
Abstract

Oligoribonucleotide ApUpG(pU)6(pA)5pAp (I) has been prepared by means of RNA ligase. ApUpG, synthesised by the phosphotriester approach, was elongated in the 3'-direction by adding (pU)6 and then (pA)6, which was 3'-blocked with the phosphate or with the periodate-oxidized AMP residue, the latter giving considerably lower level of by-products. Condensation of ApUpG(pU)6 with blocked (pA)6 was carried out under conditions optimal for poor acceptors (20 degrees C, 48 h, pH 8,7) to afford (I) with the yield of 20% (105 OE260); ApUpG(pU)6(pA)10pAp was identified as a byproduct.

摘要

寡核糖核苷酸ApUpG(pU)6(pA)5pAp (I) 是通过RNA连接酶制备的。采用磷酸三酯法合成的ApUpG在3'方向上依次添加(pU)6和(pA)6进行延伸,(pA)6的3'端用磷酸或高碘酸盐氧化的AMP残基封闭,后者产生的副产物水平明显较低。ApUpG(pU)6与封闭的(pA)6的缩合反应在对较差受体而言最优的条件下(20℃,48小时,pH 8.7)进行,得到产率为20%(105 OE260)的(I);ApUpG(pU)6(pA)10pAp被鉴定为副产物。

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