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变性双链法实现葡萄糖异构酶基因敲除的研究
引用本文:廖军,徐冲,杨永辉,李晖,程阳,陈承露,朱国萍,牛立文,王玉珍.变性双链法实现葡萄糖异构酶基因敲除的研究[J].遗传学报,2000,27(5):449-454.
作者姓名:廖军  徐冲  杨永辉  李晖  程阳  陈承露  朱国萍  牛立文  王玉珍
作者单位:1. 中国科学技术大学生命科学学院分子生物与细胞生物学系,合肥,230027
2. 中国科学技术大学结构生物学开放实验室,合肥,230027
基金项目:国家“八六三”高技术计划!( 130-13-02-04)
摘    要:对7号淀粉酶菌M1033的遗传背景进行分析,建立了其原生质体制备、转化的优化条件。构建了葡萄糖异构酶(GI)结构基因内插千方百计以链丝菌肽基因(tsr)的置换型同源重组质粒,利用其变性双链片段实现与M1033菌株染色体上基因的同源重组,获得置换型葡萄异构酶缺陷型蓖M1033LJ。为在染色体上引入突变位点实现染色体上分子定点改造造尊定了基础。

关 键 词:葡萄糖异构酶  同源重组  变性双链法  基因敲除

Glucose Isomerase Gene Knock-out by Denatured Double-stranded DNA
LIAO Jun,XU Chong,YANG Yong-Hui,LI Hui,CHENG Yang,CHEN Cheng-Lu,ZHU Guo-Ping,NIU Li-Wen,WANG Yu-Zhen.Glucose Isomerase Gene Knock-out by Denatured Double-stranded DNA[J].Journal of Genetics and Genomics,2000,27(5):449-454.
Authors:LIAO Jun  XU Chong  YANG Yong-Hui  LI Hui  CHENG Yang  CHEN Cheng-Lu  ZHU Guo-Ping  NIU Li-Wen  WANG Yu-Zhen
Abstract:After Genetic background analysis of Streptomyces diastaticus No. 7 strain M1033, the modified conditions of M1033 protoplasts and transformation were established. Replacement plasmid for homologous recombination was also constructed by inserting tsr gene into glucose isomerase gene. The homologous recombination of GI gene in M1033 chromosomes was achieved by using denatured linearized DNA fragments and glucose isomerase deficient strain M1033LJ was obtained. It is basic for introducing mutation into M1033 chromosome and realizing site-directed molecular reformation.
Keywords:glucose isomerase  Streptomyces  homologous recombination
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