首页 | 本学科首页   官方微博 | 高级检索  
   检索      

胡萝卜软腐欧文氏菌中信号分子合成酶expI基因的克隆、表达及其分析
引用本文:黄媛媛,边子睿,宋水山.胡萝卜软腐欧文氏菌中信号分子合成酶expI基因的克隆、表达及其分析[J].生物学杂志,2012,29(4):60-64.
作者姓名:黄媛媛  边子睿  宋水山
作者单位:河北省科学院生物研究所,石家庄,050081;河北省主要农作物病害微生物控制工程技术研究中心,石家庄,050081
基金项目:国家重点基础研究发展计划,河北省自然科学基金,河北省重点基础研究计划项目
摘    要:用PCR方法从胡萝卜软腐欧文氏菌的基因组DNA中扩增出信号分子合成酶expI基因,将其克隆到大肠杆菌表达载体pET-28α(+)上,转化大肠杆菌BL21(DE3),获得高效表达expI基因的重组大肠杆菌BL21(pET28α-expI).重组菌经IPTG诱导表达,SDS-PAGE检测表达蛋白相对分子质量约为24.8kD,与预期分子量相符.经薄层层析和高效液相色谱分析发现该重组菌产生的信号分子种类为N-3-羰基己酰高丝氨酸内酯和N-己酰高丝氨酸内酯与胡萝卜软腐欧文氏菌产生的一致.

关 键 词:胡萝卜软腐欧文氏菌  expI基因  克隆  薄层层析  高效液相色谱

Cloning,expression and analysis of expI gene of Erwinia carotovora subsp.carotovora
HUANG Yuan-yuan , BIAN Zi-rui , SONG Shui-shan.Cloning,expression and analysis of expI gene of Erwinia carotovora subsp.carotovora[J].Journal of Biology,2012,29(4):60-64.
Authors:HUANG Yuan-yuan  BIAN Zi-rui  SONG Shui-shan
Institution:1,2(1.Biology Institute,Hebei Academy of Sciences,Shijiazhuang 050081;2.Hebei Engineering and Technology Center of Microbiological Control on Main Crop Disease,Shijiazhuang 050081,China)
Abstract:An expI gene was amplified with PCR from the genomic DNA of Erwinia carotovora subsp.carotovora and was cloned into the expression vector pET-28 a(+).The hybrid plasmid was transformed into Escherichia coli BL21(DE3).A recombinant strain harbouring expI gene was obtained.An expression product with a molecular of 24.8kD weight was detected by SDS-PAGE after induction by IPTG.TLC and HPLC analysis revealed that the recombinant strain produced similar types of quorum sensing signals with Erwinia carotovora subsp carotorave.
Keywords:Erwinia carotovora subsp  Carotovora  expI gene  cloning  TLC  HPLC
本文献已被 CNKI 维普 万方数据 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