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Cloning and characterization of the lanosterol 14α-demethylase (ERG11) gene in Cryptococcus neoformans
被引:40
|作者:
Revankar, SG
Fu, J
Rinaldi, MG
Kelly, SL
Kelly, DE
Lamb, DC
Keller, SM
Wickes, BL
机构:
[1] Univ Texas, Hlth Sci Ctr, Dept Microbiol & Immunol, San Antonio, TX 78284 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Pathol, San Antonio, TX 78284 USA
[3] Univ Coll Swansea, Wolfson Lab P450 Biodivers, Swansea SA2 8PP, W Glam, Wales
关键词:
lanosterol demethylase;
codehop;
Candida;
Histoplasma;
Coccidioides;
D O I:
10.1016/j.bbrc.2004.09.112
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The ergosterol pathway in fungal pathogens is an attractive antimicrobial target because it is unique from the major sterol (cholesterol) producing pathway in humans. Lanosterol 14alpha-demethylase is the target for a major class of antifungals, the azoles. In this study we have isolated the gene for this enzyme from Cryptococcus neoformans. The gene, ERG11, was recovered using degenerate PCR with primers designed with a novel algorithm called CODEHOP. Sequence analysis of Erg11p identified a highly conserved region typical of the cytochrome P450 class of mono-oxygenases. The gene was present in single copy in the genome and mapped to one end of the largest chromosome. Comparison of the protein sequence to a number of major human fungal pathogen Erg11 p homologs revealed that the C. neoformans protein was highly conserved, and most closely related to the Erg11p homologs from other basidiomycetes. Functional studies demonstrated that the gene could complement a Saccharomyces cerevisiae erg11 mutant, which confirmed the identity of the C. neoformans gene. (C) 2004 Elsevier Inc. All rights reserved.
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页码:719 / 728
页数:10
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