DocumentCode :
3379488
Title :
Prokaryotic expression, protein purification of a protein phosphatase 2C gene (ZmPP2C2) from maize
Author :
Liu, Lixia ; Hu, Xiaoli
Author_Institution :
Agronomy Dept., Dezhou Univ., Dezhou, China
fYear :
2009
fDate :
13-14 Dec. 2009
Firstpage :
191
Lastpage :
193
Abstract :
The coding region of the protein phosphatase 2C gene (ZmPP2C2) from Zea mays (maize) was sub-cloned into expression vector, pET30a-c(+), and introduced into E. coli BL21 (DE3) for expression. SDS-PAGE analysis indicated ZmPP2C2 was great expressed at 37°C for 4 h with 1mM IPTG. Ultrasonic extraction experiment showed this recombinant protein was little in lysis buffer solution, but most in inclusion body. Inclusion body was collected and dissolved by lysis buffer solution with carbamide. The hexahistidine-tagged ZmPP2C2 fusion protein was purified by Ni-NTA column by 300 mM imidazole elution.
Keywords :
buffer layers; genetics; inclusions; proteins; purification; IPTG; SDS-PAGE analysis; Ultrasonic extraction experiment; carbamide; expression vector; hexahistidine-tagged ZmPP2C2 fusion protein; imidazole elution; inclusion body; lysis buffer solution; prokaryotic expression; protein phosphatase 2C gene; protein purification; temperature 37 degC; time 1 h; Amino acids; Animals; Biomedical engineering; Capacitive sensors; Cloning; Pharmaceuticals; Protein engineering; Purification; Signal processing; Stress; Imidazole elution; Prokaryotic expression; Protein phosphatase 2C; Recombinant protein;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
BioMedical Information Engineering, 2009. FBIE 2009. International Conference on Future
Conference_Location :
Sanya
Print_ISBN :
978-1-4244-4690-2
Electronic_ISBN :
978-1-4244-4692-6
Type :
conf
DOI :
10.1109/FBIE.2009.5405877
Filename :
5405877
Link To Document :
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