摘要
以耐辐射异常球菌为试材, 以 Ecoli 为对照, 用显微扫描电镜和3 H- Td R 标记, 研究了离子注入对微生物细胞的刻蚀与对 D N A 的损伤及其修复。结果表明, 注入离子对细胞存在着刻蚀损伤;中性蔗糖梯度密度离心沉降分析证明, 大剂量下离子注入可直接导致 D N A 损伤, 并观察到在对应的存活率峰值注入剂量下, Dradiodurans 修复损伤 D N A 的能力比 Ecoli 强, 还证明了细胞经不同时间温育后, 损伤的 D N A 分子得到了部分修复。
The direct action of N + implantationin on D radiodurans and E coli was investigated by SEM, and their cells were labeled with 3 H-TdR, which were implanted by 20keV N + after incubation 18hours, then the DNA of lysed cells was subjected to the neutral sucrose gradient(5%~20%) ultra-centrifugation sedimentation analysis The results showed that N + implantation exerted direct action on two kinds of microorganisms; the momentum transfer and energy deposition of implantation ions produced the direct etching damage on cells, and repair DNA efficiency of D radiodurans was higher than that of E coli Meanwhile, the damaged DNA incomplete repairing was observed When incubation was continued up to 6 hours, the rejoined DNA molecules broke again The repair of damaged DNA could be inhibited by 200μg/ml chloramphenicol This suggested that DNA damage was serious by ion implantation and damaged DNA repair of cells need continuously synthesizing repair enzyme
出处
《遗传》
CAS
CSCD
北大核心
1999年第4期37-40,共4页
Hereditas(Beijing)
基金
国家自然科学基金
关键词
离子注入
耐辐射异常球菌
DNA损伤
修复
Ion implantation
Deinococcus radiodurans
SEM
Radio-labeling
Centrifugation of neutral sucrose gradient
DNA damage and repair