鲍曼不动杆菌核苷二磷酸激酶的克隆、表达和纯化。

Q2 Biochemistry, Genetics and Molecular Biology Enzyme Research Pub Date : 2013-01-01 Epub Date: 2013-04-11 DOI:10.1155/2013/597028
Juhi Sikarwar, Sanket Kaushik, Mau Sinha, Punit Kaur, Sujata Sharma, Tej P Singh
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摘要

鲍曼不动杆菌(Acinetobacter baumannii)是一种具有多重耐药性的病原菌,与医院感染有关。这种细菌具有多种耐药机制,使得用常规药物控制这种细菌变得更加困难,而且迄今为止还没有针对这种细菌的有效药物。核苷酸二磷酸激酶是一种重要的酶,它通过将γ-磷酸从 NTPs 转移到 NDPs 来维持细胞内的三磷酸核苷酸总量。核苷二磷酸激酶(Ndk)在其他生物的致病过程中也发挥了作用。然而,要破译它在鲍曼不动杆菌中的其他可能作用,还需要进行深入研究。在本研究中,我们成功克隆了编码 Ndk 的基因,并在细菌宿主 BL-21 (DE3) 中实现了过表达。过表达的蛋白质通过镍-次氮基三乙酸(Ni-NTA)色谱法进一步纯化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cloning, Expression, and Purification of Nucleoside Diphosphate Kinase from Acinetobacter baumannii.

Acinetobacter baumannii is a multidrug resistant pathogenic bacteria associated with hospital acquired infections. This bacterium possesses a variety of resistance mechanisms which makes it more difficult to control the bacterium with conventional drugs, and, so far no effective drug treatment is available against it. Nucleoside diphosphate kinase is an important enzyme, which maintains the total nucleotide triphosphate pool inside the cell by the transfer of γ -phosphate from NTPs to NDPs. The role of nucleoside diphosphate kinase (Ndk) has also been observed in pathogenesis in other organisms. However, intensive studies are needed to decipher its other putative roles in Acinetobacter baumannii. In the present study, we have successfully cloned the gene encoding Ndk and achieved overexpression in bacterial host BL-21 (DE3). The overexpressed protein is further purified by nickel-nitrilotriacetic acid (Ni-NTA) chromatography.

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Enzyme Research
Enzyme Research Biochemistry, Genetics and Molecular Biology-Biochemistry
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