首页 | 本学科首页   官方微博 | 高级检索  
     

核多角体病毒感染昆虫细胞的DNA拓扑异构酶性质的研究
引用本文:李永方,王平,巫爱珍. 核多角体病毒感染昆虫细胞的DNA拓扑异构酶性质的研究[J]. 病毒学报, 1988, 0(4)
作者姓名:李永方  王平  巫爱珍
作者单位:中国科学院上海生物工程中心(李永方,王平),中国科学院上海生物工程中心(巫爱珍)
摘    要:核多角体病毒(Nuclear polyhedrosis virus)的核酸是双股环状DNA,在病毒颗粒中呈超螺旋状态。超螺旋DNA复制时,一般皆有超螺旋解旋过程。为了解这一机制,本文报道了从NPV感染的家蚕中肠组织中分离细胞核,经过羟基磷灰石、磷酸纤维素柱层析,ssDNA-纤维素亲和层析,纯化了DNA拓扑异构酶I,SDS-PAGE测定分子量为47kd,最适Mg~(++)浓度约为5mM。AcNPV感染的TN368细胞DNA拓扑异构酶I总活力较正常细胞酶活力高1~3倍,且活力的提高与病毒增殖平行。讨论了昆虫细胞DNA拓扑异构酶I的性质及其与NPV复制的关系。

关 键 词:核多角体病毒  超螺旋DNA  松弛型DNA  拓扑异构酶

INSECT DNA TOPOISOMERASE AND THE REPLICATION OF NPV
Li Yongfang Wang Ping Wu Aizhen. INSECT DNA TOPOISOMERASE AND THE REPLICATION OF NPV[J]. Chinese journal of virology, 1988, 0(4)
Authors:Li Yongfang Wang Ping Wu Aizhen
Affiliation:Shanghai Center of Biotechnology of Chinese Academy of Sciences
Abstract:Nuclear polyhedrosis virus ( NPV ) is one of the baculovirus which consists of supercoiled DNA in the virion. This paper describes the DNA topoisomerase I isolated from the mid-gut of silkworm , Bombyx mori and TN368 celis infected with NPV. The topoisomerase I was purified by hydroxyapatite chromatography, phosphorocellulose chromatography and DNA affinity chromatography. The molecular weight of DNA topoisomerase was 47K dalton. Mg++ was not essential but made the enzymatic activity of the DNA topoisomerase increased greatly. The activity of the DNA topoisomerase from infected TN368 celis increased parallelly with the multipli-cation of NPV. It was suggested that the DNA topoisomerase should bei-nvolved in the replication of NPV.
Keywords:Nuclear polyhedrosis virus Supercoiled DNA Relaxed DNA Topoisomerase
本文献已被 CNKI 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号