Literature DB >> 7410214

Bioconversion and biosynthesis of nanaomycins using cerulenin, a specific inhibitor of fatty acid and polyketide biosyntheses.

C Kitao, H Tanaka, S Minami, S Omura.   

Abstract

The biosynthetic relationship of the nanaomycins produced by Streptomyces rosa var. notoensis OS-3966 was studied by means of a bioconversion method using the antibiotic cerulenin, a specific inhibitor of fatty acid and polyketide biosyntheses. Nanaomycin D was considered to be the first component produced from the hypothetical intermediate "polyketide". It is proposed that the biosynthesis sequence for the nanaomycin is: nanaomycin D leads to nanaomycin A leads to nanaomycin E leads to nanaomycin B. Nanaomycin B can be converted to nanaomycin A by non-enzymatic dehydration; however, nanaomycin A is rapidly bioconverted to nanaomycin E, which is the major component synthesized by the nanaomycin-producing strain.

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Year:  1980        PMID: 7410214     DOI: 10.7164/antibiotics.33.711

Source DB:  PubMed          Journal:  J Antibiot (Tokyo)        ISSN: 0021-8820            Impact factor:   2.649


  2 in total

Review 1.  Enzymes of secondary metabolism and the biosynthesis of macrolide antibiotics.

Authors:  J Neuzil; Z Hostálek
Journal:  Folia Microbiol (Praha)       Date:  1986       Impact factor: 2.099

2.  The effect of cerulenin on the production of esperamicin A1 by Actinomadura verrucosospora.

Authors:  K S Lam; D R Gustavson; J A Veitch; S Forenza
Journal:  J Ind Microbiol       Date:  1993-02
  2 in total

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