Azole antifungals are potent inhibitors of cytochrome P450 mono-oxygenases and bacterial growth in mycobacteria and streptomycetes-Reference-Cited by-同舟云学术

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Azole antifungals are potent inhibitors of cytochrome P450 mono-oxygenases and bacterial growth in mycobacteria and streptomycetes

Published:2002-10-01 Issue:10 Volume:148 Page:2937-2949
ISSN:1350-0872
Container-title:Microbiology
language:en
Short-container-title:

Author:

McLean Kirsty J.¹,Marshall Ker R.¹,Richmond Alison²,Hunter Iain S.²,Fowler Kay³,Kieser Tobias³,Gurcha Sudagar S.⁴,Besra Gurydal S.⁴,Munro Andrew W.¹

Affiliation:

1. Department of Biochemistry, University of Leicester, The Adrian Building, University Road, Leicester LE1 7RH, UK1

2. Department of Biosciences, University of Strathclyde, The Royal College, 204 George Street, Glasgow G1 1XL, UK2

3. Department of Genetics, John Innes Centre, Norwich NR4 7UH, UK3

4. School of Biosciences, The University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK4

Publisher

Microbiology Society

Subject

Microbiology

Reference42 articles.

1. Emergence of fluconazole-resistant sterol 14-demethylase P450 (CYP51) in Candida albicans is a model demonstrating the diversification mechanism of P450;Aoyama;Arch Biochem Biophys,2000

2. Characterization and catalytic properties of the sterol 14alpha-demethylase from Mycobacterium tuberculosis;Bellamine;Proc Natl Acad Sci USA,1999

3. Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2);Bentley;Nature,2002

4. Characterization of the macrolide P-450 hydroxylase from Streptomyces venezuelae which converts narbomycin to picromycin;Betlach;Biochemistry,1998

5. Transposition of Tn 4560 of Streptomyces fradiae in Mycobacterium smegmatis;Bhatt;FEMS Microbiol Lett,2002

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