Abstract
DNA sequence analysis of a region of the Streptomyces sp. strain C5 daunomycin biosynthesis gene cluster, located between the daunomycin polyketide biosynthesis gene cluster and a dnrI (transcriptional activator) homolog, revealed the presence of a gene encoding a P-450-like enzyme with a deduced Mr of 46,096. Expression of this gene, named herein doxA, in Streptomyces lividans TY24 resulted in in vivo bioconversion of daunomycin to doxorubicin. DoxA showed specificity for only daunomycin and 13-dihydrodaunomycin, both of which were converted to doxorubicin. Daunomycinone (daunomycin aglycone), carminomycin, 13-dihydrocarminomycin, idarubicin, and aklavin were not apparent substrates for DoxA. In vector controls or in vectors in which doxA was poorly expressed, S. lividans catalyzed the reduction of daunomycin and other 13-oxo-anthracyclines and -anthracyclinones to their 13-dihydro homologs.
MeSH Terms
Amino Acid Sequence
Antibiotics, Antineoplastic/metabolism
Base Sequence
Cytochrome P-450 Enzyme System/metabolism
Daunorubicin/metabolism
Doxorubicin/metabolism
Genes, Bacterial
Molecular Sequence Data
Open Reading Frames
Plasmids
Recombinant Proteins/metabolism
Streptomyces/genetics
Substrate Specificity
Chemicals
Antibiotics, Antineoplastic
Recombinant Proteins
Doxorubicin
Cytochrome P-450 Enzyme System
Daunorubicin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Dickens M L
Department of Microbiology, The Ohio State University, Columbus, 43210, USA.
Strohl W R
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