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Preparation of fluorescence starch-nanoparticle and its application as plant transgenic vehicle

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【作者】 刘俊王凤华王玲玲肖苏尧童春意唐冬英刘选眀

【Author】 LIU Jun1, 2, WANG Feng-hua2, WANG Ling-ling3, XIAO Su-yao2, TONG Chun-yi2, TANG Dong-ying2, LIU Xuan-ming2 (1. College of Materials Science and Engineering, Hunan University, Changsha 410082, China; 2. College of Life Science and Biotechnology, Hunan University, Changsha 410082, China; 3. School of Physics and Microelectronics Science, Hunan University, Changsha 410082, China)

【机构】 College of Materials Science and Engineering,Hunan UniversityCollege of Life Science and Biotechnology,Hunan UniversitySchool of Physics and Microelectronics Science,Hunan University

【摘要】 Starch-nanoparticles were synthesized in water-in-oil microemusion at room temperature, and the starch-nanoparticles were coated with poly-L-lysine. The surface of the starch-nanoparticles was combined with fluorescence material Ru(bpy)32+·6H2O, and then the particles were characterized via transmission electron microscope. The fluorescence nanoparticles were conjugated with plasmid DNA to form complexes, and then treated with ultrasound and DNase I. pEGAD plasmid DNA-nanoparticle complexes were co-cultured with plant suspension cells of Dioscrea Zigiberensis G H Wright, and treated with ultrasound. The results show that the diameter of the fluorescence starch-nanoparticles is 50-100 nm. DNA-nanoparticle complexes can protect DNA from ultrasound damage as well as from DNase I cleavage. Mediated by ultrasound, pEGAD plasmid DNA-nanoparticle complexes can pierce into the cell wall, cell membrane and nucleus membrane of plant suspension cells. The green fluorescence protein(GFP) gene at a high frequency exceeds 5%. This nano-biomaterial can efficiently solve the problem that exterior genes cannot traverse the plant cell wall easily.

【Abstract】 Starch-nanoparticles were synthesized in water-in-oil microemusion at room temperature, and the starch-nanoparticles were coated with poly-L-lysine. The surface of the starch-nanoparticles was combined with fluorescence material Ru(bpy)32+·6H2O, and then the particles were characterized via transmission electron microscope. The fluorescence nanoparticles were conjugated with plasmid DNA to form complexes, and then treated with ultrasound and DNase I. pEGAD plasmid DNA-nanoparticle complexes were co-cultured with plant suspension cells of Dioscrea Zigiberensis G H Wright, and treated with ultrasound. The results show that the diameter of the fluorescence starch-nanoparticles is 50-100 nm. DNA-nanoparticle complexes can protect DNA from ultrasound damage as well as from DNase I cleavage. Mediated by ultrasound, pEGAD plasmid DNA-nanoparticle complexes can pierce into the cell wall, cell membrane and nucleus membrane of plant suspension cells. The green fluorescence protein(GFP) gene at a high frequency exceeds 5%. This nano-biomaterial can efficiently solve the problem that exterior genes cannot traverse the plant cell wall easily.

【基金】 Project(200501) supported the “985” Program of China
  • 【文献出处】 Journal of Central South University of Technology ,中南工业大学学报(英文版) , 编辑部邮箱 ,2008年06期
  • 【分类号】Q943.2
  • 【被引频次】10
  • 【下载频次】57
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