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PMID: 10658662 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Elucidation of anthracyclinone biosynthesis by stepwise cloning of genes for anthracyclines from three different Streptomyces spp.

Microbiology (Reading, England) ·Vol. 146 ( Pt 1) ·2000-01-00 ·Pages 155-163

Kantola J, Kunnari T, Hautala A, Hakala J, Ylihonko K, Mäntsälä P

Abstract

The anthracycline skeleton is biosynthesized by aromatic (type II) polyketide synthases. Furthermore, three post-polyketide steps are needed to form the basic aglycone of anthracyclines. Auramycinone was produced in Streptomyces lividans by introducing nine structural genes from three different anthracycline-producing Streptomyces species. The genes used to construct the auramycinone biosynthesis cluster were derived from nogalamycin-, daunomycin- and aclacinomycin-producing Streptomyces strains. The biosynthetic stages were divided into polyketide and post-polyketide steps on the assumption that the first stable intermediate would be nogalonic acid, named analogously to aklanonic acid, the precursor of several anthracyclines. Single genes were cloned in the expression construct in the order determined by the proposed biosynthetic pathway. This facilitated investigation of the products formed in the heterologous host after addition of each separate gene to the construct. The results thus elucidate the biosynthesis steps, products and the genes responsible for the reactions needed to build up an anthracyclinone.

MeSH Terms
Anthracyclines/chemistry,metabolism Antibiotics, Antineoplastic/biosynthesis,chemistry Cloning, Molecular Escherichia coli/genetics,metabolism Genes, Bacterial Magnetic Resonance Spectroscopy Molecular Sequence Data Multigene Family Open Reading Frames Plasmids/genetics Streptomyces/genetics,metabolism
Chemicals
Anthracyclines Antibiotics, Antineoplastic auramycinone
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Kantola Jaana
Department of Biochemistry, University of Turku, Vatselantie 2, FIN-20014 Turku, Finland1.
Kunnari Tero
Galilaeus Oy, PO BOX 113, FIN-20781 Kaarina, Finland2.
Hautala Anne
Galilaeus Oy, PO BOX 113, FIN-20781 Kaarina, Finland2.
Hakala Juha
Galilaeus Oy, PO BOX 113, FIN-20781 Kaarina, Finland2.
Ylihonko Kristiina
Galilaeus Oy, PO BOX 113, FIN-20781 Kaarina, Finland2. | Department of Biochemistry, University of Turku, Vatselantie 2, FIN-20014 Turku, Finland1.
Mäntsälä Pekka
Department of Biochemistry, University of Turku, Vatselantie 2, FIN-20014 Turku, Finland1.
Article Info
Journal
Microbiology (Reading, England)
Abbr.
Microbiology (Reading)
ISSN
1350-0872
Published
2000-01-00
Pages
155-163
Language
English
Region
England
NLM ID
9430468
Subset
IM
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