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多核苷酸磷酸化酶体外从头合成类DNA分子

De Novo Synthesis of DNA-Like Molecules by Polynucleotide Phosphorylase In Vitro.

作者信息

Beljanski M

机构信息

Cerbiol Application, Centre de Recherche Biologique, Domaine de la Source, Saint-Prim 38370, France

出版信息

J Mol Evol. 1996 May;42(5):493-9. doi: 10.1007/BF02352279.

Abstract

In the presence of Mg2+ ions, polynucleotide phosphorylase (PNPase, EC 2.7.7.8) is known to synthesize RNA-like polymers using ribonucleoside-5'-diphosphate (NDP) substrates but to be unable to utilize deoxyribonucleoside substrates. Our experiments show that when MgCl2 is replaced by FeCl3, PNPase becomes able to synthesize deoxyheteropolymers using deoxyribonucleoside-5'-diphosphates (dNDPs). The deoxyheteropolymer formed from the four dNDPs is degraded by pancreatic DNase, but not by RNase, and is readily used as a template by DNA-dependent DNA polymerase. Synthesis of this DNA-like polymer is accomplished de novo without the help of any primer or preexisting template. What is more, dA/dG and dC/dT ratios of polymers synthesized by different bacterial PNPases closely match ratios found in DNA of the bacterial species the enzyme came from.

摘要

已知在镁离子存在的情况下,多核苷酸磷酸化酶(PNPase,EC 2.7.7.8)利用核糖核苷-5'-二磷酸(NDP)底物合成类RNA聚合物,但无法利用脱氧核糖核苷底物。我们的实验表明,当用氯化铁取代氯化镁时,PNPase能够利用脱氧核糖核苷-5'-二磷酸(dNDPs)合成脱氧杂聚物。由四种dNDP形成的脱氧杂聚物可被胰脱氧核糖核酸酶降解,但不能被核糖核酸酶降解,并且很容易被依赖DNA的DNA聚合酶用作模板。这种类DNA聚合物的合成是从头开始完成的,无需任何引物或预先存在的模板。此外,不同细菌的PNPase合成的聚合物的dA/dG和dC/dT比率与该酶来源的细菌物种的DNA中发现的比率密切匹配。

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