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变铅青链霉菌多核苷酸磷酸化酶在磷酸解条件下能够聚合核苷二磷酸,这对结构 RNA 的降解有影响。

Streptomyces coelicolor polynucleotide phosphorylase can polymerize nucleoside diphosphates under phosphorolysis conditions, with implications for the degradation of structured RNAs.

机构信息

Department of Biochemistry and Molecular Biology, The University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

J Bacteriol. 2013 Nov;195(22):5151-9. doi: 10.1128/JB.00936-13. Epub 2013 Sep 13.

Abstract

We have examined the ability of wild-type polynucleotide phosphorylase (PNPase) from Streptomyces coelicolor and two mutant forms of the enzyme, N459D and C468A, to function in the polymerization of ADP and in the phosphorolysis of RNA substrates derived from the S. coelicolor rpsO-pnp operon. The wild-type enzyme was twice as active in polymerization as N459D and four times as active as C468A. The kcat/Km value for phosphorolysis of a structured RNA substrate by N459D was essentially the same as that observed for the wild-type enzyme, while C468A was 50% as active with this substrate. A mixture of all four common nucleoside diphosphates increased the kcat/Km for phosphorolysis of the structured substrate by the wild-type enzyme by a factor of 1.7 but did not affect phosphorolysis catalyzed by N459D or C468A. We conducted phosphorolysis of the structured substrate in the presence of nucleoside diphosphates and labeled the 3' ends of the products of those reactions using [(32)P]pCp. Digestion of the end-labeled RNAs and display of the products on a sequencing gel revealed that wild-type S. coelicolor PNPase was able to synthesize RNA 3' tails under phosphorolysis conditions while the N459D and C468A mutants could not. The wild-type enzyme did not add 3' tails to a substrate that already possessed an unstructured 3' tail. We propose a model in which the transient synthesis of 3' tails facilitates the phosphorolysis of structured substrates by Streptomyces PNPase.

摘要

我们研究了野生型多核苷酸磷酸化酶(PNPase)、两种突变酶 N459D 和 C468A 在聚合 ADP 和磷酸解 RNA 底物方面的功能,这些 RNA 底物来自链霉菌 coelicolor 的 rpsO-pnp 操纵子。野生型酶在聚合反应中的活性是 N459D 的两倍,是 C468A 的四倍。N459D 对结构 RNA 底物的磷酸解的 kcat/Km 值与野生型酶观察到的基本相同,而 C468A 对此底物的活性为 50%。四种常见的核苷二磷酸混合物使野生型酶对结构底物的磷酸解的 kcat/Km 值提高了 1.7 倍,但不影响 N459D 或 C468A 催化的磷酸解。我们在存在核苷二磷酸的情况下进行了结构底物的磷酸解,并使用 [(32)P]pCp 标记这些反应产物的 3'末端。对末端标记的 RNA 进行消化并在测序凝胶上显示产物,结果表明野生型链霉菌 PNPase 能够在磷酸解条件下合成 RNA 3'尾巴,而 N459D 和 C468A 突变体则不能。野生型酶不会向已经具有无结构 3'尾巴的底物添加 3'尾巴。我们提出了一个模型,其中 3'尾巴的瞬时合成有助于链霉菌 PNPase 对结构底物的磷酸解。

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