Objective The aim was to explore conditions of genetic transformation for Indica rice Kasalath and laid a foundation for further study on molecular biology. Method With callus of Kasalath as transformation receptor,...Objective The aim was to explore conditions of genetic transformation for Indica rice Kasalath and laid a foundation for further study on molecular biology. Method With callus of Kasalath as transformation receptor, Agrobacterium tumefaciens-mediated method was used to conduct genetic transformation. The genetic transformation system was optimized from several aspects, including co-culture mode, co-culture time and the affertreatment method of co-culture. Result The results showed that two days is the best co-culture time for genetic transformation, the acquisition rate of resistant callus was up to 84.1%, and transformation rate was up to 73%. Whether callus contact to the culture medium directly or indirectly has no significant effect on transformation. [ Conclusion] Genetic transformation successfully transferred exogenous gene OsMAPk2 into the rice genome.展开更多
[Objective] The research aimed to provide reference for increasing the genetic transformation efficiency of Ginkgo biloba mediated by Agrobacterium.[Method] Taking the mature embryos of Ginkgo biloba seeds as explants...[Objective] The research aimed to provide reference for increasing the genetic transformation efficiency of Ginkgo biloba mediated by Agrobacterium.[Method] Taking the mature embryos of Ginkgo biloba seeds as explants,after 48 hours＇ pre-cultivation on MS medium in the absence of phytohormone,GUS gene was transmitted into embryos of Ginkgo biloba mediated by three kinds of Agrobacterium.Transient expression of GUS gene activity was observed through histochemical staining,and the influencing factors of the expression of GUS gene were analyzed.And the expression vector of 1-deoxy-D-xylulose-5-phosphate reductoisomerase in the biosynthesis approach of biobalide precursor of Ginkgo biloba was constructed.[Result] A more suitable genetic transformation scheme was obtained as follows：taking embryos of Ginkgo biloba as explants,using EHA105 Agrobacterium with pCAMBIA1304＋ for infection,co-culture for 3 days and GUS staining.The results showed that transient expression rate of GUS after transformation was higher.[Conclusion] The research provide a more effective method for further study on the transgene of Ginkgo biloba.展开更多
In order to achieve large tolerance capture and high stiffness connection for space payload operations,a Chinese large-scale space end-effector (EER) was developed.Three flexible steel cables were adopted to capture t...In order to achieve large tolerance capture and high stiffness connection for space payload operations,a Chinese large-scale space end-effector (EER) was developed.Three flexible steel cables were adopted to capture the payload with large capture allowance.Ball screw transmission mechanism and plane shape-constraint four bar linkage mechanism were utilized to connect the payload with high stiffness.The experiments show that capture tolerances in X,Y,Z,Pitch,Yaw,Roll directions are 100 mm,100 mm,120 mm,10.5°,10.5°,12°,respectively.The maximum connection stiffness is 4 800 N·m.The end-effector could meet the requirements for space large tolerance capture and high stiffness connection in the future.展开更多
In this paper, populus xeuramericana cv. Guariento was transformed with bean chitinase by Agrobacterium tumefaciens-mediated leaf disc method. Firstly, the leaf explants were pre-cultured at 25℃ for 2d. Secondly, the...In this paper, populus xeuramericana cv. Guariento was transformed with bean chitinase by Agrobacterium tumefaciens-mediated leaf disc method. Firstly, the leaf explants were pre-cultured at 25℃ for 2d. Secondly, they were infected in Agrobacterium tumefaciens suspension （OD600=0.5） for 20 rain, then were co-cultured for 3d in the dark. Thirdly, the explants were transferred to the selection culture medium （containing Kanamycin 40 mg.L^-1 and Cefotaxime Sodium 800 mg-L1） and incubated at 25℃ until resistance buds formed. Chitinase activity was determined for the positive plants by PCR and PCR-Southern blot hybridization analysis. And, chitinase activity of positive plants was significantly higher than that of control plant, and the highest ratio of activity of NO.4 to that of control was 3.41. It showed that bean chitinase gene had been expressed in the plant genome.展开更多
基金Supported by Youth Foundation of National Natural Science(30600400)Chenguang Program of Youth Science and Techonogyof Wuhan City(00750731302)Introduced Talents Started Projectof South-Central University for Nationalities(YZZ05012)~~
文摘Objective The aim was to explore conditions of genetic transformation for Indica rice Kasalath and laid a foundation for further study on molecular biology. Method With callus of Kasalath as transformation receptor, Agrobacterium tumefaciens-mediated method was used to conduct genetic transformation. The genetic transformation system was optimized from several aspects, including co-culture mode, co-culture time and the affertreatment method of co-culture. Result The results showed that two days is the best co-culture time for genetic transformation, the acquisition rate of resistant callus was up to 84.1%, and transformation rate was up to 73%. Whether callus contact to the culture medium directly or indirectly has no significant effect on transformation. [ Conclusion] Genetic transformation successfully transferred exogenous gene OsMAPk2 into the rice genome.
文摘[Objective] The research aimed to provide reference for increasing the genetic transformation efficiency of Ginkgo biloba mediated by Agrobacterium.[Method] Taking the mature embryos of Ginkgo biloba seeds as explants,after 48 hours＇ pre-cultivation on MS medium in the absence of phytohormone,GUS gene was transmitted into embryos of Ginkgo biloba mediated by three kinds of Agrobacterium.Transient expression of GUS gene activity was observed through histochemical staining,and the influencing factors of the expression of GUS gene were analyzed.And the expression vector of 1-deoxy-D-xylulose-5-phosphate reductoisomerase in the biosynthesis approach of biobalide precursor of Ginkgo biloba was constructed.[Result] A more suitable genetic transformation scheme was obtained as follows：taking embryos of Ginkgo biloba as explants,using EHA105 Agrobacterium with pCAMBIA1304＋ for infection,co-culture for 3 days and GUS staining.The results showed that transient expression rate of GUS after transformation was higher.[Conclusion] The research provide a more effective method for further study on the transgene of Ginkgo biloba.
基金Project(2006AA04Z228) supported by the National High Technology Research and Development Program of China
文摘In order to achieve large tolerance capture and high stiffness connection for space payload operations,a Chinese large-scale space end-effector (EER) was developed.Three flexible steel cables were adopted to capture the payload with large capture allowance.Ball screw transmission mechanism and plane shape-constraint four bar linkage mechanism were utilized to connect the payload with high stiffness.The experiments show that capture tolerances in X,Y,Z,Pitch,Yaw,Roll directions are 100 mm,100 mm,120 mm,10.5°,10.5°,12°,respectively.The maximum connection stiffness is 4 800 N·m.The end-effector could meet the requirements for space large tolerance capture and high stiffness connection in the future.
基金This work was supported by Heilongjiang Key Technologies R＆D Programme （No. GB06B303-4） and Heilongjiang Natural Science Foundation（No. ZJN04-0101）.
文摘In this paper, populus xeuramericana cv. Guariento was transformed with bean chitinase by Agrobacterium tumefaciens-mediated leaf disc method. Firstly, the leaf explants were pre-cultured at 25℃ for 2d. Secondly, they were infected in Agrobacterium tumefaciens suspension （OD600=0.5） for 20 rain, then were co-cultured for 3d in the dark. Thirdly, the explants were transferred to the selection culture medium （containing Kanamycin 40 mg.L^-1 and Cefotaxime Sodium 800 mg-L1） and incubated at 25℃ until resistance buds formed. Chitinase activity was determined for the positive plants by PCR and PCR-Southern blot hybridization analysis. And, chitinase activity of positive plants was significantly higher than that of control plant, and the highest ratio of activity of NO.4 to that of control was 3.41. It showed that bean chitinase gene had been expressed in the plant genome.
