Martin E M, Sonnabend J A
J Virol. 1967 Feb;1(1):97-109. doi: 10.1128/JVI.1.1.97-109.1967.
The large-particle fraction from the cytoplasm of chick embryo fibroblasts infected with Semliki Forest virus was found to catalyze the incorporation of the 5'-triphosphates of guanosine, adenine, cytidine, and uridine into an acid-insoluble alkali-labile product. The conditions affecting the preparation and assay of this enzyme were investigated. The ribonucleic acid (RNA) polymerase was not present in uninfected cells, and it appeared in infected cells at the time of rapid viral RNA synthesis. The polymerase was found to catalyze the synthesis of a species of RNA which was resistant to ribonuclease and which exhibited the sedimentation properties, buoyant density, and thermal transition temperature of the double-stranded RNA found in vivo in chick cells infected with Semliki forest virus. Attempts to demonstrate that the reaction product of this enzyme also included single-stranded viral RNA were not successful. Although other interpretations are possible, these results give some support to the suggestion that more than one enzyme may be involved in the replication of viral RNA.
研究发现,感染了Semliki森林病毒的鸡胚成纤维细胞胞质中的大颗粒部分能催化鸟苷、腺嘌呤、胞苷和尿苷的5'-三磷酸掺入一种酸不溶性碱不稳定产物中。对影响该酶制备和测定的条件进行了研究。未感染细胞中不存在核糖核酸(RNA)聚合酶,它在病毒RNA快速合成时出现在感染细胞中。发现该聚合酶能催化一种对核糖核酸酶有抗性的RNA的合成,这种RNA表现出与感染Semliki森林病毒的鸡细胞体内双链RNA相同的沉降特性、浮力密度和热转变温度。证明该酶的反应产物还包括单链病毒RNA的尝试未成功。尽管可能有其他解释,但这些结果为病毒RNA复制可能涉及不止一种酶的观点提供了一些支持。