[Objective] The research aimed to study the seed germination and growth of different rape cultivars, including Brassica napus, Brassica juncea and Brassica rapa, treated with kanamycin or hygromycin at different conce...[Objective] The research aimed to study the seed germination and growth of different rape cultivars, including Brassica napus, Brassica juncea and Brassica rapa, treated with kanamycin or hygromycin at different concentrations. [Method] Brassica napus Chun K101, Brassica napus L0935 and Brassica rapa L0926 seeds were cultured on 1/2 MS medium supplemented with different concentrations of antibiotics. The hypocotyl and taproot changes of different rape cultivated were recorded and analyzed. [Result] It was shown that 50 mg/L kanamycin could stimulate rapeseed hypocotyl growth, but obviously restrain taproot development. Hygromycin apparently inhibited the growth of hypocotyl and taproot of all the three cultivars. [Conclusion] Kanamycin was suitable to screen the transformed seed of Brassica juncea. The optimal concentration of hygromycin to screen transgenic rapeseed was 40-60 mg/L.展开更多
[ Objective] The study is to generate pharmaceutical protein via plant transgenic technique. [Methed] Using the cotyledons with petiole as transformation receptor, the fusion gene of rapeseed oil-body gene and bFGF wa...[ Objective] The study is to generate pharmaceutical protein via plant transgenic technique. [Methed] Using the cotyledons with petiole as transformation receptor, the fusion gene of rapeseed oil-body gene and bFGF was introduced into the rapeseed （ Brassica campestris L. ） by Agrobacterium tumefaciens-mediated transformation; meanwhile regeneration conditions of rapeseed were also optimized, and the regenerated resistant plantlets were detected by PCR and Southern blot. [ Result] This fusion gene had been integrated into rapeseed genome successfully, and the optimized conditions of transformation and regeneration were as follows： explants pre-culture for 2 d, co-culture for 3 d, bacteria solution OD600 for 0.3 and infection time for 5 min. [ Conclusion] The results laid a solid foundation for extraction, isolation and purification of protein in transgenic plant seeds.展开更多
[Objective]The aim was to explore the relative expression trends of WRKY transcription factor gene under ABA treatment in Brassica campestris.[Method]Actin gene and WRKY gene were cloned by using the homology cloning ...[Objective]The aim was to explore the relative expression trends of WRKY transcription factor gene under ABA treatment in Brassica campestris.[Method]Actin gene and WRKY gene were cloned by using the homology cloning method.The sequences of nucleic acid and amino acid were analyzed using BLAST and DNAMAN software.Relative expression trends of WRKY gene were detected by applying real-time relative quantification PCR（RT-qPCR）under ABA（100 μmol/L）treatment.[Result]A 680 bp WRKY gene segment and a 933 bp β-actin gene segment were acquired in Brassica campestris.The result of RT-qPCR analysis revealed that BcWRKY expression could be induced by ABA and that the relative expression of WRKY gene reached the peak at 1 h with ABA treatment.[Conclusion]Actin and WRKY gene in B.campestris were cloned successfully,which was proved to play an important role in ABA signal pathway.展开更多
基金Supported by the National High Technology Research and Development Program of China(863Program,2007AA10Z120)the Doctoral Fund of Henan Polytechnic University(B2011-035)~~
文摘[Objective] The research aimed to study the seed germination and growth of different rape cultivars, including Brassica napus, Brassica juncea and Brassica rapa, treated with kanamycin or hygromycin at different concentrations. [Method] Brassica napus Chun K101, Brassica napus L0935 and Brassica rapa L0926 seeds were cultured on 1/2 MS medium supplemented with different concentrations of antibiotics. The hypocotyl and taproot changes of different rape cultivated were recorded and analyzed. [Result] It was shown that 50 mg/L kanamycin could stimulate rapeseed hypocotyl growth, but obviously restrain taproot development. Hygromycin apparently inhibited the growth of hypocotyl and taproot of all the three cultivars. [Conclusion] Kanamycin was suitable to screen the transformed seed of Brassica juncea. The optimal concentration of hygromycin to screen transgenic rapeseed was 40-60 mg/L.
基金Supported by Bioreactor Important Special Item of 863-Program inthe "Eleventh Five-Year" Plan (No. 2007AA100503)Science and Technology Development Key Plan of Jilin Province( No.20070922)+1 种基金Cultivation Fund of Scientific and Technical Innovation Project Major Program of Higher Education Institutions ( No.70S018)Science and Technology Plan of Changchun City (No.06GG150)~~
文摘[ Objective] The study is to generate pharmaceutical protein via plant transgenic technique. [Methed] Using the cotyledons with petiole as transformation receptor, the fusion gene of rapeseed oil-body gene and bFGF was introduced into the rapeseed （ Brassica campestris L. ） by Agrobacterium tumefaciens-mediated transformation; meanwhile regeneration conditions of rapeseed were also optimized, and the regenerated resistant plantlets were detected by PCR and Southern blot. [ Result] This fusion gene had been integrated into rapeseed genome successfully, and the optimized conditions of transformation and regeneration were as follows： explants pre-culture for 2 d, co-culture for 3 d, bacteria solution OD600 for 0.3 and infection time for 5 min. [ Conclusion] The results laid a solid foundation for extraction, isolation and purification of protein in transgenic plant seeds.
基金Supported by Plant Stress Biology Research Platform Establishment Program of Beijing Municipal Education Commission(5075101019)~~
文摘[Objective]The aim was to explore the relative expression trends of WRKY transcription factor gene under ABA treatment in Brassica campestris.[Method]Actin gene and WRKY gene were cloned by using the homology cloning method.The sequences of nucleic acid and amino acid were analyzed using BLAST and DNAMAN software.Relative expression trends of WRKY gene were detected by applying real-time relative quantification PCR（RT-qPCR）under ABA（100 μmol/L）treatment.[Result]A 680 bp WRKY gene segment and a 933 bp β-actin gene segment were acquired in Brassica campestris.The result of RT-qPCR analysis revealed that BcWRKY expression could be induced by ABA and that the relative expression of WRKY gene reached the peak at 1 h with ABA treatment.[Conclusion]Actin and WRKY gene in B.campestris were cloned successfully,which was proved to play an important role in ABA signal pathway.
