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Fusion Expression of Raphanus sativus-Antifungal Protein 1 (Rs-AFP1) in Escherichia coli and Its Antifungal Activity on Verticillium dahliae 被引量:3
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作者 周向军 王仑山 +4 位作者 林芝萍 贾军伟 卢山 储昭庆 陈晓亚 《Acta Botanica Sinica》 CSCD 2000年第7期703-707,共5页
The Raphanus sativus L. antifungal protein 1 (Rs_AFP1) gene was isolated by polymerase chain reaction (PCR). The complete open reading frame and the fragment encoding the putative mature protein were inserted into the... The Raphanus sativus L. antifungal protein 1 (Rs_AFP1) gene was isolated by polymerase chain reaction (PCR). The complete open reading frame and the fragment encoding the putative mature protein were inserted into the prokaryotic expression vector pET_32b(+), respectively. Subsequent expression showed that the Rs_AFP1 was produced in E. coli as a 27 kD fusion protein only when the N_terminal signal peptide was removed. After treatment with thrombin to remove part of the N_terminal His.tag sequence, the bacterially expressed Rs_AFP1 was used for fungal growth inhibition assay which was conducted on Verticillium dahliae Kleb., a soil_born fungus causing the cotton wilt disease. Results showed that, in the liquid medium, the Rs_AFP1 fusion protein at a concentration of 0.3 g/L clearly inhibited the growth of V. dahliae and the germination of spores. Thus the bacterially expressed fusion protein had the antifungal activity against V. dahliae. 展开更多
关键词 Raphanus sativus_antifungal protein 1 (rs-afp1) FUNGUS Verticillium dahliae prokaryotic expression
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农杆菌介导将抗真菌r-硫堇蛋白Rs-afp1基因导入水稻获得转基因植株 被引量:5
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作者 姚方印 李广贤 +3 位作者 杨磊 刘理梅 李中华 翟红梅 《山东农业科学》 2002年第3期20-21,共2页
利用农杆菌介导的高效遗传转化系统 ,将抗真菌r -硫堇蛋白Rs -afp1基因导入黄淮稻区主栽品种豫梗 6号的胚性愈伤组织 ,获得了 8株转基因植株 ,Gus染色和PCR分析表明 。
关键词 农杆菌介导 rs-afp1基因 水稻 转基因植株 r-硫堇蛋白 稻瘟病 纹枯病 抗病育种 真菌
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农杆菌介导AFP1基因转化小麦获得转基因植株 被引量:5
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作者 支大英 徐春晖 +3 位作者 薛哲勇 刘庆忠 姜鸿鸣 夏光敏 《山东农业科学》 2004年第3期14-16,19,共4页
以nptⅡ基因为筛选基因,利用农杆菌转化系统向普通小麦品种核生3号和99P的愈伤组织中转入白粉病抗性基因Rs-AFP1;获得抗生素抗性克隆数目分别为27个和24个,其中再生绿苗的克隆分别为2个和8个;PCR分析检测所得nptⅡ阳性植株分别为2株和6... 以nptⅡ基因为筛选基因,利用农杆菌转化系统向普通小麦品种核生3号和99P的愈伤组织中转入白粉病抗性基因Rs-AFP1;获得抗生素抗性克隆数目分别为27个和24个,其中再生绿苗的克隆分别为2个和8个;PCR分析检测所得nptⅡ阳性植株分别为2株和6株,AFP1基因阳性植株分别为1株和4株。 展开更多
关键词 普通小麦 农杆菌介导转化 转基因植株 rs-afp1
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