Khan Z A, Hiriyanna K T, Chavez F, Fraenkel-Conrat H
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2383-6. doi: 10.1073/pnas.83.8.2383.
Much work has been done on the isolation, purification, and characterization of the RNA-directed RNA polymerase (EC 2.7.7.48) of cucumber mosaic virus (CMV)-infected cucumbers. Uninfected plants were reported to have no such enzyme, but we recently detected low levels of the activity in cucumber. Since tobacco and cowpea contain such an enzyme that is variably increased in amount by various virus (as well as viroid) infections, we assumed that this would also be the case upon CMV infection of cucumber. However, further purification and characterization of the RNA-directed RNA polymerases from healthy and from infected cucumber suggests that these are different enzymes. The presumed CMV replicase was obtained pure and consists of a major polypeptide of Mr 100,000 and minor components of Mr 110,000 and about 10,000. The Km is 5 microM ([3H]GTP) when tobacco mosaic virus RNA is used as template.
在黄瓜花叶病毒(CMV)感染的黄瓜中,针对RNA指导的RNA聚合酶(EC 2.7.7.48)的分离、纯化及特性研究已经开展了大量工作。据报道,未感染的植物没有这种酶,但我们最近在黄瓜中检测到了低水平的该酶活性。由于烟草和豇豆含有这种酶,且其含量会因各种病毒(以及类病毒)感染而不同程度地增加,我们推测黄瓜感染CMV后也会出现这种情况。然而,对健康黄瓜和感染黄瓜中RNA指导的RNA聚合酶的进一步纯化和特性分析表明,它们是不同的酶。假定的CMV复制酶已被纯化出来,它由一个分子量为100,000的主要多肽以及分子量为110,000和大约10,000的次要成分组成。当以烟草花叶病毒RNA作为模板时,其米氏常数(Km)为5微摩尔([3H]GTP)。