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苏云金芽孢杆菌NAD(P)H:醌氧化还原酶基因的克隆和敲除载体的构建
引用本文:李今煜,肖水华,黄天培.苏云金芽孢杆菌NAD(P)H:醌氧化还原酶基因的克隆和敲除载体的构建[J].福建农林大学学报(自然科学版),2012,41(5):508-512.
作者姓名:李今煜  肖水华  黄天培
作者单位:福建农林大学生物农药与化学生物学教育部重点实验室,福建福州,350002
基金项目:国家自然科学基金,国家863项目,福建省高校服务海西建设重点项目
摘    要:以苏云金芽孢杆菌库斯塔克亚种(Bacillus thuringiensis subsp.kurstaki)8010为研究材料,通过PCR技术获得Bt 8010菌株NAD(P)H:醌氧化还原酶基因上下游2个片段,以含有卡那霉素抗性基因的pDG780质粒为中间载体,通过酶切、连接和PCR,构建含待敲除NAD(P)H:醌氧化还原酶基因上下游片段、卡那霉素抗性基因的重组质粒pRN5101DKU,为后续Bt8010菌株NAD(P)H:醌氧化还原酶基因的敲除做准备.

关 键 词:苏云金芽孢杆菌  NAD(P)H:醌氧化还原酶基因  基因敲除载体

Cloning and knockout vector construction of a NAD(P)H: quinone oxidoreductase gene in Bacillus thuringiensis
LI Jin-yu , XIAO Shui-hua , HUANG Tian-pei.Cloning and knockout vector construction of a NAD(P)H: quinone oxidoreductase gene in Bacillus thuringiensis[J].Journal of Fujian Agricultural and Forestry University,2012,41(5):508-512.
Authors:LI Jin-yu  XIAO Shui-hua  HUANG Tian-pei
Institution:(Key Laboratory of Biopesticide and Chemical Biology,Ministry of Education, Fujian Agriculture and Forestry University,Fuzhou,Fujian 350002,China)
Abstract:Bacillus thuringiensis subsp.kurstaki isolate 8010 was selected to obtain the upstream and downstream sequences of NAD(P)H: quinone oxidoreductase gene by PCR technology.The pDG780 vector(containing the kanamycin resistance gene) was used to construct a recombination plasmid pRN5101DKU which contained the upstream and downstream sequences of NAD(P)H: quinone oxidoreductase,and the kanamycin resistance gene by PCR and RE treatments.It was provided for further study on gene knockout.
Keywords:Bacillus thuringiensis  NAD(P)H: quinone oxidoreductase gene  gene knockout vector
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