The treatment of muskmelon cultivar 'Wangwenxiang', which is sensitive to watermelon mosaic virus-2 (WMV-2), with oxalate increases systemic resistance of the cultivar to WMV-2 significantly. The challenge ino...The treatment of muskmelon cultivar 'Wangwenxiang', which is sensitive to watermelon mosaic virus-2 (WMV-2), with oxalate increases systemic resistance of the cultivar to WMV-2 significantly. The challenge inoculation experiments indicate that the symptom of ox-alate-treated plant is much slighter than that of control plants and the virus content is only 4%展开更多
Endo-β-glucanase II(EG II)gene cDNA was isolated from the fungus Humicola insolens H31-3 by RT-PCR.It was cloned into the expression vector pGAPZαA.The resultant recombinant plasmid was introduced into Pichia pastor...Endo-β-glucanase II(EG II)gene cDNA was isolated from the fungus Humicola insolens H31-3 by RT-PCR.It was cloned into the expression vector pGAPZαA.The resultant recombinant plasmid was introduced into Pichia pastoris GS115 by electroporation after being linearized by BspHI digestion.The recombinant Pichia pastoris strain was obtained and SDS-PAGE showed that the molecular weight of the expression protein was about 55 kD.The cultivation condition and the characteristics of the recombinant EG II were also explored.展开更多
文摘The treatment of muskmelon cultivar 'Wangwenxiang', which is sensitive to watermelon mosaic virus-2 (WMV-2), with oxalate increases systemic resistance of the cultivar to WMV-2 significantly. The challenge inoculation experiments indicate that the symptom of ox-alate-treated plant is much slighter than that of control plants and the virus content is only 4%
基金This work was funded by the National Plan Key Technology R&D Program of China(No.2004BA713B03-01).
文摘Endo-β-glucanase II(EG II)gene cDNA was isolated from the fungus Humicola insolens H31-3 by RT-PCR.It was cloned into the expression vector pGAPZαA.The resultant recombinant plasmid was introduced into Pichia pastoris GS115 by electroporation after being linearized by BspHI digestion.The recombinant Pichia pastoris strain was obtained and SDS-PAGE showed that the molecular weight of the expression protein was about 55 kD.The cultivation condition and the characteristics of the recombinant EG II were also explored.
