New products related to kinamycin from Streptomyces murayamaensis. II. Structures of pre-kinamycin, keto-anhydrokinamycin, and kinamycins E and F.
- 1 January 1989
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 42 (2) , 189-197
- https://doi.org/10.7164/antibiotics.42.189
Abstract
Four new colored components of Streptomyces murayamaensis sp. nov. Hata et Ohtani, the producer of the kinamycins, have been isolated and their structures determined by a combination of mass spectral, high field NMR and biosynthetic techniques. The first compound with the benz[b]carbazole skeleton in the biosynthetic pathway of kinamycin D has been named "pre-kinamycin" (7). A keto-epoxide kinamycin intermediate has been labeled "keto-anhydrokinamycin" (9), and the 1''-monoacetate of kinamycin has been called kinamycin E (12). Natural production of deacetylkinamycin (13, now labeled kinamycin F) by S. murayamaensis has been confirmed by an isotope trapping experiment. The role of these new intermediates in kinamycin biosynthesis is discussed.This publication has 2 references indexed in Scilit:
- New products related to kinamycin from Streptomyces murayamaensis. I. Taxonomy, production, isolation and biological properties.The Journal of Antibiotics, 1989
- Biosynthesis of the kinamycin antibiotics by Streptomyces murayamaensis. Determination of the origin of carbon, hydrogen, and oxygen atoms by carbon-13 NMR spectroscopyJournal of the American Chemical Society, 1986