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Generation of Pesticides-degrading Genetically Engineered Bacteria Expressing the Protein of GFP and Carboxylesterase B1

机译:产生杀虫剂降解的遗传工程细菌表达GFP和羧酸酶B1的蛋白质

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The genetically engineered bacteria, expressing the fusion protein of enhanced green fluorescent protein (EGFP) and carboxylesterase B1, have been successfully constructed, by cloning the genes of EGFP and carboxylesterase B1 into the pET-28b vector and then transforming E. coli BL21 (DE3). Expression of the fusion protein can be induced in E. coli BL21 (DE3) at 28°C for 8h by even as little as 0.01mM isopropyl β-D-thiogalactopyranoside (IPTG). The genetically engineered bacteria not only can degrade pesticides in the environment but also can be found easily by fluorescence spectrophotometry. The green fluorescence emitted by EGFP in genetically engineered bacteria can be seen even by naked eye in daylight.
机译:通过将EGFP和羧基酶B1的基因克入PET-28B载体,转化大肠杆菌BL21(DE3 )。融合蛋白的表达可以在28℃下在大肠杆菌BL21(DE3)中诱导8小时,甚至只有0.01mM异丙基β-D-硫代酰甲酸钠(IPTG)。转基因细菌不仅可以降解环境中的杀虫剂,而且可以通过荧光分光光度法容易地发现。甚至可以在白天的肉眼看到eGFP在遗传工程细菌中发出的绿色荧光。

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