Document Detail


Expression and purification of recombinant arginine decarboxylase (speA) from Escherichia coli.
MedLine Citation:
PMID:  19603287     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The crystal structures of almost all the enzymes of arginine metabolism have been determined, but arginine decarboxylase's structure is not resolved yet. In order to characterize and crystallize arginine decarboxylase, we overexpressed biosynthetic arginine decarboxylase (ADC; EC 4.1.1.19, encoded by the speA gene) from Escherichia coli in the T7 expression system as a cleavable poly-His-tagged fusion construct. The expressed recombinant His(10)-ADC (77.3 kDa) was first purified by Ni-NTA affinity chromatography, then proteolytically digested with Tobacco Etch Virus (TEV) protease to remove the poly-His fusion tag, and finally purified by anion exchange chromatography. The His(10) tag removed recombinant ADC (74.1 kDa)'s typical yield was 90 mg from 1 l of culture medium with purity above 98%. The recombinant ADC was assayed for decarboxylase activity, showing decarboxylase activity of 2.8 U/mg, similar to the purified native E. coli ADC. The decarboxylase activity assay also showed that the purified recombinant ADC tolerated broad ranges of pH (pH 6-9) and temperature (20-80 degrees C). Our research may facilitate further studies of ADC structure and function, including the determination of its crystal structure by X-ray diffraction.
Authors:
Jiaping Song; Chuanwen Zhou; Rui Liu; Xudong Wu; Di Wu; Xiaojian Hu; Yu Ding
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-07-15
Journal Detail:
Title:  Molecular biology reports     Volume:  37     ISSN:  1573-4978     ISO Abbreviation:  Mol. Biol. Rep.     Publication Date:  2010 Apr 
Date Detail:
Created Date:  2010-03-03     Completed Date:  2010-06-08     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0403234     Medline TA:  Mol Biol Rep     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  1823-9     Citation Subset:  IM    
Affiliation:
Department of Physiology and Biophysics, School of Life Sciences, Fudan University, 200433, Shanghai, China.
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MeSH Terms
Descriptor/Qualifier:
Carboxy-Lyases / isolation & purification*,  metabolism*
Cloning, Molecular
Culture Media
Electrophoresis, Polyacrylamide Gel
Escherichia coli / enzymology*
Escherichia coli Proteins / isolation & purification*,  metabolism*
Genetic Vectors / genetics
Hydrogen-Ion Concentration
Open Reading Frames
Recombinant Fusion Proteins / isolation & purification*,  metabolism*
Temperature
Chemical
Reg. No./Substance:
0/Culture Media; 0/Escherichia coli Proteins; 0/Recombinant Fusion Proteins; EC 4.1.1.-/Carboxy-Lyases; EC 4.1.1.19/arginine decarboxylase

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