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14型鼻病毒RNA聚合酶复合物

Rhinovirus type 14 RNA polymerase complexes.

作者信息

Griffith M M, Gauntt C J

出版信息

Arch Virol. 1975;47(1):11-20. doi: 10.1007/BF01315588.

Abstract

Rhinovirus type 14 RNA-dependent RNA polymerase complexes were isolated from microsomal and soluble fraction of infected KB cells. Maximum activities were measured at at 6 and 7 hours post inoculation (p.i.) for microsomal and soluble polymerases, respectively. Both polymerase activities are considerably reduced by 8 to 9 hours, p.i., and interval in which the in vivo rate of synthesis of viral RNA is maximal. In vitro RNA products of RNA polymerases in both fractions consist of ribonuclease-sensitive and ribonuclease-resistant RNA of heterogeneous sizes. Detergent treatment of the microsomal RNA polymerase(s) did not affect the total amount of RNA synthesized, the proportion of ribonuclease-sensitive RNA synthesized or the size of the RNA products. The data suggest that RV14RNA polymerase complexes are intially associated with membranes but are then irreversibly released into the soluble phase of the cytoplasm; possible explanations for this phenomena are discussed.

摘要

从感染的KB细胞的微粒体和可溶部分中分离出14型鼻病毒RNA依赖性RNA聚合酶复合物。微粒体和可溶聚合酶的最大活性分别在接种后6小时和7小时测得。两种聚合酶活性在接种后8至9小时显著降低,而这一时间段内病毒RNA的体内合成速率最高。两个部分中RNA聚合酶的体外RNA产物均由大小各异的核糖核酸酶敏感型和核糖核酸酶抗性RNA组成。用去污剂处理微粒体RNA聚合酶不会影响合成的RNA总量、合成的核糖核酸酶敏感型RNA的比例或RNA产物的大小。数据表明,RV14 RNA聚合酶复合物最初与膜结合,但随后不可逆地释放到细胞质的可溶相中;文中讨论了对此现象的可能解释。

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