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Discovery of a pimaricin analog JBIR-13, from Streptomyces bicolor NBRC 12746 as predicted by sequence analysis of type I polyketide synthase gene.
Komaki, Hisayuki; Izumikawa, Miho; Ueda, Jun-ya; Nakashima, Takuji; Khan, Shams Tabrez; Takagi, Motoki; Shin-ya, Kazuo.
Affiliation
  • Komaki H; Biomedicinal Information Research Center, Japan Biological Informatics Consortium, 2-42 Aomi, Koto-ku, Tokyo 135-0064, Japan. hskomaki@nbrc.nite.go.jp
Appl Microbiol Biotechnol ; 83(1): 127-33, 2009 May.
Article in En | MEDLINE | ID: mdl-19156407
ABSTRACT
Sequence analysis of ketosynthase domain amplicons from Streptomyces bicolor NBRC 12746(T) revealed the presence of previously unreported type I polyketide synthases (PKS-I) genes. The clustering of these genes with the reference PKS-1 sequences suggested the possibility to produce a polyene compound similar to pimaricin. Thus, the cultured sample from NBRC 12746(T) was analyzed for the production of polyene compounds. The strain produced an antifungal compound which displayed the UV absorption spectrum of tetraene macrolides. The structure determination based on the spectroscopic analysis of the purified compound resulted in the identification of a novel pimaricin analog JBIR-13 (1). This study therefore strongly suggested that a careful analysis of PKS-I genes can provide valuable information in the search of novel bioactive compounds within a class predicted from phylogenetic analysis.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Streptomyces / Bacterial Proteins / Natamycin / Polyketide Synthases / Antifungal Agents Type of study: Prognostic_studies / Risk_factors_studies Language: En Year: 2009 Type: Article

Full text: 1 Database: MEDLINE Main subject: Streptomyces / Bacterial Proteins / Natamycin / Polyketide Synthases / Antifungal Agents Type of study: Prognostic_studies / Risk_factors_studies Language: En Year: 2009 Type: Article