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Cloning, Expression, and Purification of Nucleoside Diphosphate Kinase fromAcinetobacter baumannii
Author(s) -
Juhi Sikarwar,
Sanket Kaushik,
M. Sinha,
Punit Kaur,
Sujata Sharma,
T.P. Singh
Publication year - 2013
Publication title -
enzyme research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.439
H-Index - 39
eISSN - 2090-0406
pISSN - 2090-0414
DOI - 10.1155/2013/597028
Subject(s) - acinetobacter baumannii , cloning (programming) , nucleoside , nucleoside diphosphate kinase , microbiology and biotechnology , virology , biology , medicine , kinase , bacteria , genetics , computer science , pseudomonas aeruginosa , programming language
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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