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丝裂霉素C对Erwinia herbicola表达及运转冰核活性蛋白方式的影响
引用本文:陈庆森,高秀芝,闫亚丽,宋丽萍,庞广昌,郭淑华.丝裂霉素C对Erwinia herbicola表达及运转冰核活性蛋白方式的影响[J].遗传学报,2005,32(5):545-549.
作者姓名:陈庆森  高秀芝  闫亚丽  宋丽萍  庞广昌  郭淑华
作者单位:1. 天津市食品生物技术重点实验室,天津商学院,天津,300134
2. 北京农学院食品科学与工程系,北京,100012
3. 天津南开大学实验中心,天津,300071
基金项目::国家自然科学基金资助(编号:39770580),国家自然科学基金资助(主任基金)(编号:30340040),天津市重点自然科学基金(编号:023803311)资助~~
摘    要:利用添加丝裂霉素C(MMC)于不同培养基中,并在不同培养条件下对草生欧文氏菌10025A(E.herbicola 10025A)诱导培养,首次证实该菌表达冰核活性蛋白的活性及运转分泌冰核活性蛋白方式是不同。研究结果显示,MMC的加入可以提高细菌培养物的冰核活性,该现象可以解释为MMC对E.herbicola的作用能够激活细胞SOS应急系统的反应,诱导细胞合成部分参与修复DNA损伤的酶和蛋白因子,达到对E.herbicola诱导表达冰核蛋白通过高尔基体形成小液泡,向膜外分泌的方式,同时对E.herbicola细胞分裂后的形态也发生明显的影响。这对研究细胞在恶劣环境的生存机制以及获取该条件下的蛋白具有重要的意义,对低温生物的研究也将产生积极地影响。

关 键 词:丝裂霉素C  诱导  冰核活性细菌  冰核活性蛋白  扫描电镜
文章编号:0379-4172(2005)05-0545-05

Effects of Mitomycin C on the Expression and Transport of Ice-nuclei Proteins of Erwinia herbicola
CHEN Qing-sen,GAO Xiu-Zhi,YAN Ya-li,SONG Li-ping,PANG Guang-chang,GUO Shu-hua.Effects of Mitomycin C on the Expression and Transport of Ice-nuclei Proteins of Erwinia herbicola[J].Journal of Genetics and Genomics,2005,32(5):545-549.
Authors:CHEN Qing-sen  GAO Xiu-Zhi  YAN Ya-li  SONG Li-ping  PANG Guang-chang  GUO Shu-hua
Institution:CHEN Qing-Sen~
Abstract:In this paper,Mitomycin C (MMC) was added to different kinds of medium to study the effects of different cultural conditions on the Erwinia herbicola 10025A.For the first time it was confirmed that the expressed activity of the ice-nuclei active protein was different from its transportable manner from the ice nucleation active bacteria (Erwinia herbicola 10025A).The findings indicated that MMC could stimulate the SOS response,and induce the synthesis of some enzymes and proteins,which take part in repairing the damaged DNA.The effects of the MMC on the E.herbicola under different media were different.It could increase the ice nucleation activity of the E.herbicola,forming new small vesicles,which are secreted to the outside of membrane.The importance of this research for study the living mechanism of cells ander poor condition was discussed.
Keywords:Mitomycin C  induction  ice nucleation active bacteria  ice-nuclei active protein  scanning electronic microscope
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