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RNA催化的硫酯合成。

RNA-catalyzed thioester synthesis.

作者信息

Coleman Tricia M, Huang Faqing

机构信息

Department of Chemistry and Biochemistry, University of Southern Mississippi, Hattiesburg, MS 39406, USA.

出版信息

Chem Biol. 2002 Nov;9(11):1227-36. doi: 10.1016/s1074-5521(02)00264-8.

Abstract

A series of efficient ribozymes with thioester synthetase activities have been isolated from CoA-linked RNA libraries containing four different lengths (30N, 60N, 100N, and 140N) of random nucleotide regions. Competitive evolution of these size-heterogeneous CoA-RNA libraries resulted in an RNA size population in the order of 30N > 60N >> 100N > 140N. From isolated clones in the 30N and 60N size groups, two predominant RNA sequences, TES1 (30N) and TES33 (60N), have been shown to catalyze the synthesis of different thioesters using various acyl adenylates as the substrates. Together with our previous findings, the current results demonstrate a CoA thioester synthetic pathway catalyzed by individual metabolic ribozymes, and suggest a likely mechanism for thioester synthesis and utilization in an RNA world.

摘要

一系列具有硫酯合成酶活性的高效核酶已从包含四种不同长度(30N、60N、100N和140N)随机核苷酸区域的CoA连接RNA文库中分离出来。这些大小异质的CoA-RNA文库的竞争性进化导致RNA大小群体的顺序为30N > 60N >> 100N > 140N。从30N和60N大小组中分离出的克隆中,已证明两种主要的RNA序列TES1(30N)和TES33(60N)使用各种酰基腺苷酸作为底物催化不同硫酯的合成。结合我们之前的发现,目前的结果证明了由单个代谢核酶催化的CoA硫酯合成途径,并提出了RNA世界中硫酯合成和利用的可能机制。

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