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重组抗菌肽LfcinB/LfampinB基因的克隆及表达载体的构建
引用本文:孙金霞,刘艳环,李海涛,李庆超,张广雷,苗利光. 重组抗菌肽LfcinB/LfampinB基因的克隆及表达载体的构建[J]. 特产研究, 2010, 32(2): 16-18,39
作者姓名:孙金霞  刘艳环  李海涛  李庆超  张广雷  苗利光
作者单位:1. 江苏科技大学,江苏镇江,212018;中国农业科学院特产研究所,吉林吉林,132109
2. 中国农业科学院特产研究所,吉林吉林,132109
3. 江苏科技大学,江苏镇江,212018
基金项目:中国农业科学院特产研究所基金 
摘    要:根据GeneBank中提供的牛乳铁蛋白基因序列,设计并合成了重组LfcinB/LfampinB基因,并通过PGEM-Teasy载体扩增。酶切回收的LfcinB/LfampinB片段与中间载体pP6连接。pP6上的启动子、信号肽和调控序列与LfcinB/LfampinB共同切下,获得具有上游调控元件的PLfc/Lfa基因片段。将PLfc/Lfa与pME290表达载体连接,并转化绿脓杆菌。结果表明,本试验成功构建了重组pPLfc/Lfa表达载体。

关 键 词:抗菌肽  克隆  表达载体  构建

The Cloing and Expressional Vector Construction of Recombinant Antimicrobial peptide LfcinB/LfampinB Gene
SUN Jin-xia,LIU Yan-huan,LI Hai-tao,Li Qing-chao,ZHANG Guang-lei,MIAO Li-guang. The Cloing and Expressional Vector Construction of Recombinant Antimicrobial peptide LfcinB/LfampinB Gene[J]. Special Wild Economic Animal and Plant Research, 2010, 32(2): 16-18,39
Authors:SUN Jin-xia  LIU Yan-huan  LI Hai-tao  Li Qing-chao  ZHANG Guang-lei  MIAO Li-guang
Affiliation:1.Jiangsu University of Science and Technology,Zhenjiang 212018,China;2.Institute of Special Wild Economic Animals and Plants CAAS,Jilin 132109,China)
Abstract:the Bovine lactoferrin gene deposited in GeneBank,LfcinB/LfampinB recombinant gene was designed and synthesized,and then amplified by PGEM-T easy plasmid.The purified LfcinB/LfampinB gene by restriction enzyme was linked to pP6 plasmid.Together with LfcinB/LfampinB gene,the promoter,signal peptide and regulator gene which were in pP6 plasmid were digested by restriction enzyme,PLfc/Lfa fragment which had upstream regulatory element was obtained.PLfc/Lfa was linked to pME290 expression plasmid and transformed into competent cells of.The results showed that recombinant expression plasmid pPLfc/Lfa was obtained.
Keywords:Antimicrobial peptide  Clone  Expressional plasmid  Construction
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