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首页> 外文期刊>Applied and Environmental Microbiology >Construction and use of a nontoxigenic strain of Pseudomonas aeruginosa for the production of recombinant exotoxin A.
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Construction and use of a nontoxigenic strain of Pseudomonas aeruginosa for the production of recombinant exotoxin A.

机译:铜绿假单胞菌非产毒菌株的构建和生产重组外毒素A的用途。

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To express recombinant forms of Pseudomonas aeruginosa exotoxin A in high yield, we have developed a nontoxigenic strain of P. aeruginosa derived from the hypertoxigenic strain PA103. The nontoxigenic strain, designated PA103A, was produced by the excision marker rescue technique to replace the toxA structural gene in PA103 with an insertionally inactivated toxA gene. The PA103A strain (ToxA-) was used subsequently as the host strain for the expression and production of several recombinant versions of exotoxin A, and the results were compared with exotoxin A production in other P. aeruginosa and Escherichia coli strains. Use of the PA103A strain transformed with the high-copy-number pRO1614 plasmid bearing various toxA alleles resulted in final purification yields of exotoxin A averaging 23 mg/liter of culture. By comparison, exotoxin A production in other expression systems and host strains yields approximately 1/4 to 1/10 as much toxin.
机译:为了高产量表达铜绿假单胞菌外毒素A的重组形式,我们开发了一种来自高毒原性菌株PA103的铜绿假单胞菌的非毒原性菌株。通过切除标记拯救技术生产了非毒素菌株,命名为PA103A,用插入灭活的toxA基因代替了PA103中的toxA结构基因。随后将PA103A菌株(ToxA-)用作宿主菌株,以表达和生产几种重组形式的外毒素A,并将该结果与其他铜绿假单胞菌和大肠杆菌菌株中外毒素A的产生进行比较。使用带有多个toxA等位基因的高拷贝数pRO1614质粒转化的PA103A菌株可产生平均23毫克/升培养物的外毒素A的最终纯化产量。相比之下,在其他表达系统和宿主菌株中外毒素A的产生量大约是毒素的1/4至1/10。

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