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链霉菌分化关键基因——whiG在大肠杆菌的克隆和高表达 被引量:1
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作者 谭华荣 田宇清 +4 位作者 杨海花 吴畏 董可宁 K F Chater M J Buttner 《中国科学(B辑)》 CSCD 北大核心 1995年第11期1167-1171,共5页
whiG结构基因翻译起始位点邻近的序列区域被改造了6个碱基。利用聚合酶链式反应(PCR)扩增了该基因,序列分析验证了改造后的整个DNA序列,并定向克隆到大肠杆菌高效表达载体pET11c的T7噬菌体10启动子的下游,转化可被IPTG诱导产生T7 RNA聚... whiG结构基因翻译起始位点邻近的序列区域被改造了6个碱基。利用聚合酶链式反应(PCR)扩增了该基因,序列分析验证了改造后的整个DNA序列,并定向克隆到大肠杆菌高效表达载体pET11c的T7噬菌体10启动子的下游,转化可被IPTG诱导产生T7 RNA聚合酶的受体菌株——大肠杆菌BL21(DE3)。诱导后的重组菌株,经蛋白提取,SDS-PAGE结果表明whiG在大肠杆菌中获得了高效表达,其表达量约为不溶性蛋白总量的20%。经抗体制备,Western杂交证明了高效表达的产物确是whiG的编码产物——σ^(whiG)。whiG基因被亚克隆到链霉菌的表达质粒载体pIJ6021,转化天蓝色链霉菌孢子形成缺陷突变株C71后,使其能恢复孢子的形成,进一步证明了改造后的whiG基因的生物学功能。 展开更多
关键词 链霉菌 分化 σ^whiG 大肠杆菌 基因表达 克隆
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High-level expression of whiG——A key gene for Streptomyces differentiation in Escherichia coli
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作者 谭华荣 田宇清 +3 位作者 杨海花 吴畏 董可宁 K. F. Chater and M. J. Buttner 《Science China(Life Sciences)》 SCIE CAS 1996年第3期284-290,共7页
Six nucleotides located in the region of translation start site of whiG were changed. whiG was amplified by PCR technique. Reformed sequences were determined. This gene was directly subcloned into expression vector pE... Six nucleotides located in the region of translation start site of whiG were changed. whiG was amplified by PCR technique. Reformed sequences were determined. This gene was directly subcloned into expression vector pET11c containing strong T7 promoter, and the recombinant plasmid was introduced into E. coli BL21(DE3), which could be induced by IPTG to produce T7 RNA polymerase. The SDS-PAGE result showed that whiG highly expressed in E. coli BL21(DE3), and the yield of whiG product was about 20% of insoluble proteins in cell. whiG product (σwhiG) was further identified by Western blot hybridization after making its antibody. whiG gene was subcloned into Streptomyces plasmid pIJ6021, and then it was introduced into sporulation deficient mutant C71 from Streptomyces coelicolor. The result showed that C71 could restore sporulation and σwhiG has biological functions. 展开更多
关键词 Streptomyces differentiation σ^(whiG) high expression.
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