Back to Search Start Over

Expression and characterization of the carboxyl esterase Rv3487c from Mycobacterium tuberculosis

Authors :
Zhang, Min
Wang, Jia-dong
Li, Zuo-feng
Xie, Jun
Yang, Yan-ping
Zhong, Yang
Wang, Hong-hai
Source :
Protein Expression & Purification. Jul2005, Vol. 42 Issue 1, p59-66. 8p.
Publication Year :
2005

Abstract

Abstract: Rv3487c (lipF), a member of the lipase family of Mycobacterium tuberculosis, is related to virulence of this pathogen. Real-time RT-PCR analysis indicated that Rv3487c was induced at low pH in M. tuberculosis cultured in vitro. The gene of Rv3487c was cloned and expressed as fusion protein in Escherichia coli. After removal of the N-terminal domain of the fusion partner by enterokinase treatment, the effect of pH, temperature, and detergents on the purified enzyme activity and stability was characterized. Rv3487c could efficiently hydrolyze short chain esters. The catalytic triad of Rv3487c consists of residues Ser90, Glu189, and His219 as demonstrated by amino acid sequence alignment, three-dimensional modeling, and site-directed mutagenesis. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
10465928
Volume :
42
Issue :
1
Database :
Academic Search Index
Journal :
Protein Expression & Purification
Publication Type :
Academic Journal
Accession number :
17920368
Full Text :
https://doi.org/10.1016/j.pep.2005.03.022