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Development of Wolffia arrhiza as a Producer for Recombinant Human Granulocyte Colony-Stimulating Factor

机译:开发作为重组人粒细胞集落刺激因子生产者的无花果。

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To date, the expression of recombinant proteins in transgenic plants is becoming a powerful alternative to classical expression methods. Special efforts are directed to the development of contained cultivation systems based on cell culture or rhyzosecretion, which reliably prevents the heterologous DNA releasing into the environment. A promising object for the development of such systems is the tiny aquatic plant of wolffia (Wolffia arrhiza (L.) Horkel ex Wimm.), which can be used as a dipped culture in bioreactors. Herein we have expressed the human granulocyte colony-stimulating factor (hG-CSF) in nuclear-transformed wolffia. The nucleotide sequence of hG-CSF was optimized for expression in wolffia and cloned into the vector pCamGCSF downstream of double CaMV 35S promoter. Wolffia plants were successfully transformed and 34 independent transgenic lines with hG-CSF gene were obtained, PCR and Southern blot analysis confirmed the transgenic origin of these lines. Western blot analysis revealed accumulation of the target protein in 33 transgenic lines. Quantitative ELISA of protein extracts from these lines showed hG-CSF accumulation up to 35.5 mg/kg of wolffia raw weight (0.194% of total soluble protein). This relatively high yield holds promise for the development of wolffia-based expression system in strictly controlled format to produce various recombinant proteins.
机译:迄今为止,重组蛋白在转基因植物中的表达正成为经典表达方法的有力替代方法。专门致力于开发基于细胞培养或根分泌的封闭式培养系统,该系统可可靠地防止异源DNA释放到环境中。开发这种系统的有前途的对象是狼f(Wolffia arrhiza(L.)Horkel ex Wimm。)的微小水生植物,其可用作生物反应器中的浸入式培养物。在此,我们已经在核转化的狼疮中表达了人类粒细胞集落刺激因子(hG-CSF)。优化了hG-CSF的核苷酸序列以在狼疮中表达,并将其克隆到双CaMV 35S启动子下游的载体pCamGCSF中。成功地转化了Wolffia植物,并获得了34个具有hG-CSF基因的独立转基因株系,PCR和Southern blot分析证实了这些株系的转基因起源。 Western印迹分析揭示了靶蛋白在33个转基因系中的积累。从这些品系提取的蛋白质的定量ELISA结果显示,hG-CSF积累的狼毒原重高达35.5 mg / kg(占总可溶性蛋白的0.194%)。这种相对较高的产量有望为严格控制形式的基于沃尔夫亚的表达系统的开发提供希望,以产生各种重组蛋白。

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