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真菌诱导型植物表达载体pBP的构建

Construction of Fungi Inducible Plant Expression Vector pBP
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摘要 根据prp1-1启动子序列设计并合成了一对引物,通过PCR扩增的方法从马铃薯基因组中扩增到了病原诱导的prp1-1启动子,并将其克隆到PGEMT-Easy载体上,然后进一步克隆到植物表达载体pBI101.2上,构建了病原诱导型基因表达载体pBP. According to the reported sequences of inducible expression promoter prp1 - 1, a pair of primers were designed and synthesised. After the fragment of prp1 - 1 promoter was amplified by the method of PCR from the potato, it was inserted into PGEMT- Easy vector. Thereafter, the fragment was cloned into pBI101. 2 expression vector, and a new kind of pathogen - inducible expression vector pBP was constructed.
出处 《湛江师范学院学报》 2005年第3期37-40,共4页 Journal of Zhanjiang Normal College
基金 广东省科技计划项目(Z002A2070402) 湛江市科技攻关项目(103).
关键词 诱导型启动子 prp1-1 克隆 载体构建 fungi - inducible promoter prp1 - 1 cloning vector construction
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参考文献1

  • 1Norbert Martini,Margot Egen,Irmgard Rüntz,Günter Strittmatter. Promoter sequences of a potato pathogenesis-related gene mediate transcriptional activation selectively upon fungal infection[J] 1993,MGG Molecular & General Genetics(2-3):179~186

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