[The use of nucleolytic enzymes (ribonucleases, polynucleotide phosphorylases and endonuclease from Serratia marcescens) for producing initial blocks of synthetic endoribonucleases].

V P Kliagina, E A Sedel'nikova, O A Smolianinova, I A Soboleva, M I Khabarova, S M Zhenodarova
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引用次数: 0

Abstract

The simplest variant of synthetic substrate-ribozyme complex has been proposed. The schemes of potential ribozyme "subunits" synthesis have been worked out: R1--GCUUGAAACAAA; R2--AAAAACUGAUGAAAGC. The macroscale synthesis of dinucleoside monophosphate ApU, GpC, CpU catalyzed by immobilized ribonucleases of different specificity and preparation of oligoadenylates by hydrolysis of poly-A in the presence of endonuclease Serratia marcescens, as well the synthesis of conservative sequences of potential ribozyme such as ApUpG, CpUpG, GpApU, ApApApG and others have been described.

[利用溶核酶(来自粘质沙雷氏菌的核糖核酸酶、多核苷酸磷酸化酶和核酸内切酶)产生合成核糖核酸内切酶的初始片段]。
提出了合成底物-核酶复合物的最简单变体。确定了潜在核酶亚基的合成方案:R1—GCUUGAAACAAA;R2——AAAAACUGAUGAAAGC。本文描述了不同特异性的固定化核糖核酸酶催化大尺度合成单磷酸二核苷ApU、GpC、CpU,在粘质沙雷菌核酸内切酶存在下水解聚a制备低聚腺苷酸,以及潜在核酶保守序列ApUpG、CpUpG、GpApU、ApApApG等的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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