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植物病毒沉默抑制子P25的原核表达及纯化
引用本文:秦波,麻鹏达,伏秀青,杨涛,刘晶莹,董春光,王兴智.植物病毒沉默抑制子P25的原核表达及纯化[J].吉林农业大学学报,2005,27(4):378-380.
作者姓名:秦波  麻鹏达  伏秀青  杨涛  刘晶莹  董春光  王兴智
作者单位:东北师范大学遗传与细胞研究所,长春,130024
基金项目:国家自然科学基金资助项目(30370767)
摘    要:通过体外DNA重组技术将P25基因连接在pET28a(+)载体上,构建成重组质粒。经PCR扩增、酶切鉴定及DNA序列分析,融合的P25基因序列正确。将重组质粒转化到大肠杆菌BL21(DE3)中进行异丙基β-D硫代半乳糖苷(IPTG)诱导表达,经过亲和层析得到纯品目的蛋白P25。

关 键 词:基因沉默抑制子  P25蛋白  原核表达系统
文章编号:1000-5684(2005)04-0378-03
收稿时间:2005-01-07
修稿时间:2005-01-07

Expression of A RNA Silencing Suppressor in Eschcrichia coli and Its Purification
QIN Bo,MA Peng-Da,FU Xiu-qing,YANG Tao,LIU Jing-ying,DONG Chun-guang,WANG Xing-zhi.Expression of A RNA Silencing Suppressor in Eschcrichia coli and Its Purification[J].Journal of Jilin Agricultural University,2005,27(4):378-380.
Authors:QIN Bo  MA Peng-Da  FU Xiu-qing  YANG Tao  LIU Jing-ying  DONG Chun-guang  WANG Xing-zhi
Abstract:The P25 gene was inserted into the pET-28a(+) vector to create a recombinant plasmid pET-28a(+)-P25. The resulted recombinant DNA was verified by PCR, restriction enzyme digestion and DNA sequencing. The P25 protein was then expressed in Eschcrichia coli and purified by Ni-NTA affinity chromatography after being induced by IPTG under denaturing condition.
Keywords:RNA silencing suppressor  P25 protein  prokaryotic expression system
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