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A型产气荚膜梭菌α-毒素基因的克隆与核苷酸序列分析
引用本文:赵志军,许崇波,曾瑾,邓光存,王玉炯. A型产气荚膜梭菌α-毒素基因的克隆与核苷酸序列分析[J]. 生物技术, 2003, 13(4): 1-2
作者姓名:赵志军  许崇波  曾瑾  邓光存  王玉炯
作者单位:宁夏大学生命科学学院,宁夏,银川,750021
基金项目:宁夏自然科学基金资助项目("α毒素基因工程亚单位苗的研制",200206)
摘    要:利用聚合酶链式反应(PCR)技术,从A型产气莫膜梭菌染色体基因组中扩增了1.2kb的α毒素基因。通过T4 DNA连接酶,将纯化的PCR产物与载体pGEM-T连接,转化受至体菌JM109中,经NcoI/EcoRI和BamHI/EcoRI双酶切分析,证明重组质粒pXCPA02中含有A型产气荚膜棱菌α毒素全基因。经核苷酸序列分析,明确了克隆的α毒素基因在重组质粒中的连接向位且核苷酸序列是正确的。

关 键 词:A型产气荚膜梭菌 α-毒素 基因克隆 核苷酸序列分析
文章编号:1004-311X(2003)04-0001-02
修稿时间:2003-03-16

Cloning and Nucleotide Sequencing of alpha-toxin Gene of Clostridium perfringens typeA
ZHAO Zhi-Jun,XU Chong-Bo,ZENG Jing,DENG Guang-cun,WANG Yu-Jiong. Cloning and Nucleotide Sequencing of alpha-toxin Gene of Clostridium perfringens typeA[J]. Biotechnology, 2003, 13(4): 1-2
Authors:ZHAO Zhi-Jun  XU Chong-Bo  ZENG Jing  DENG Guang-cun  WANG Yu-Jiong
Abstract:Alpha-toxin gene was amplified from genomic DNA of Clostridium perfringens type A by polymerase chain reaction(PCR).PCR product was inserted into vector pGEM-T directively.The recombinant plasmid pXCPA02 was identified by restriction endonucleases Nco I/ Eco RI and Bam HI/ Eco RI analysis and nucleotide sequencing.The results showed that alpha-toxin gene fragment of 1.2kb has been cloned with a positive nucleotide sequence.
Keywords:Clostridium perfringens type A  alpha-toxin gene  gene cloning  nucleotide sequence
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