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机构地区:[1]中国热带农业科学院热带作物生物技术国家重点实验室
出 处:《热带作物学报》1995年第S1期83-88,共6页Chinese Journal of Tropical Crops
摘 要:利用带有Trp启动子的大肠杆菌表达载体WCC8能有效地表达西红柿Cu/ZnSOD基因,该表达蛋白在菌体中具有活性,并在一定程度上抑制受体菌SOD基因的表达。据SDS-PAGE分析,表达SOD蛋白占茵体总蛋白20%左右,其活性达3.0×105V/L发酵液。还利用NBT法对表达SOD蛋白的活性进行了研究。The CV/Zn SOD(superoxide dismutase)gene of Tomato has been successfully cloned and ex-pressed in E. coli under the transcriptional control of the Trp promoters. The expression protein ofSOD gene prOduced was as much as 20%of total cellular protein by SDS-pAGE eletrophoresisand it showed activity in the host ceIls of E. coli by NBT method,while the expression of SODgene of the host cells was greatly inhibited.It was demonstrated that 3.0 × 105 U activity of SODcould be obtained from 1 LB medium after fermentation for 10h.
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