Stone H O, Portner A, Kingsbury D W
J Virol. 1971 Aug;8(2):174-80. doi: 10.1128/JVI.8.2.174-180.1971.
Sendai virions contain an enzyme which catalyzes the incorporation of ribonucleotides into ribonucleic acid (RNA). Enzyme activity was optimal at pH 8.0 and 28 C; otherwise conditions were similar to those reported for Newcastle disease virion (NDV) RNA polymerase. The initial rate of RNA synthesis by the Sendai virion enzyme was about 10 pmoles per mg of protein per hr, but after 3 hr of incubation the rate increased about fivefold. The virion enzyme was compared with an RNA polymerase in the microsomal fraction of infected cells. Both enzymes made predominantly single-stranded RNA which was complementary in base sequences to 50S virion RNA. Most of the RNA synthesized by the virion polymerase sedimented at 16S, but the product of the microsomal enzyme sedimented at about 8S.
仙台病毒粒子含有一种能催化核糖核苷酸掺入核糖核酸(RNA)的酶。酶活性在pH 8.0和28℃时最佳;其他条件与报道的新城疫病毒粒子(NDV)RNA聚合酶的条件相似。仙台病毒粒子酶合成RNA的初始速率约为每毫克蛋白质每小时10皮摩尔,但孵育3小时后速率增加约五倍。将病毒粒子酶与感染细胞微粒体部分中的RNA聚合酶进行了比较。两种酶主要合成单链RNA,其碱基序列与50S病毒粒子RNA互补。病毒粒子聚合酶合成的大部分RNA在16S处沉降,但微粒体酶的产物在约8S处沉降。