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作 者:WANG Zhongni LIU Huijing LI Luhua LI Quanliang WANG Xiuran JIANG Yuan FU Yuqin LU Changli
机构地区:[1]Engineering Research Center of Bioreactor and Pharmaceutical Development, Ministry of Education,College of Life Science, Jilin Agricultural University, Changchun 130018, P R. China [2]Faculty of Chemistry, Northeast Normal University, Changchun 130024, P. R. China [3]Guizhou Sub-center of National Wheat Improvement Center, Guizhou University, Guiyang 550025, P. R. China
出 处:《Chemical Research in Chinese Universities》2017年第6期912-916,共5页高等学校化学研究(英文版)
基 金:Supported by the National Natural Science Foundation of China(Nos.31302062, 21074019) and the Youth Fund of Jilin Agricultural University, China(No.201315).
摘 要:Although nanotechnology is considered to be one of the most important technologies to promote social and economic development in the twenty-first century, its application in agriculture is relatively few compared with those in other fields. In this article, plasmid carrying GUS gene was successfully delivered into tobacco(Nicotiana tabacum) by mesoporous silica nanoparticles(MSNs) modified with positively charged poly-L-lysine(PLL) with the assist of ultrasonic method. Stable transformation was confirmed by polymerase chain reaction(PCR) detection and GUS histochemical staining. Meanwhile, we also studied the factors that could enhance the genetic transformation efficiency. The result suggests that the callus receptor and a suitable DNA/MSNs ratio contribute a lot to the transformation efficiency. In a word, our research provides an efficient and cost-effective method for gene delivery to plant.Although nanotechnology is considered to be one of the most important technologies to promote social and economic development in the twenty-first century, its application in agriculture is relatively few compared with those in other fields. In this article, plasmid carrying GUS gene was successfully delivered into tobacco(Nicotiana tabacum) by mesoporous silica nanoparticles(MSNs) modified with positively charged poly-L-lysine(PLL) with the assist of ultrasonic method. Stable transformation was confirmed by polymerase chain reaction(PCR) detection and GUS histochemical staining. Meanwhile, we also studied the factors that could enhance the genetic transformation efficiency. The result suggests that the callus receptor and a suitable DNA/MSNs ratio contribute a lot to the transformation efficiency. In a word, our research provides an efficient and cost-effective method for gene delivery to plant.
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