4.5 Article

Novel bioactive metabolites from a marine derived bacterium Nocardia sp ALAA 2000

Journal

JOURNAL OF ANTIBIOTICS
Volume 61, Issue 6, Pages 379-386

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ja.2008.53

Keywords

Nocardia sp ALAA 2000; ayamycin; justicidin B; NMR; X-ray; antimicrobial

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Extracts of the Egyptian marine actinomycete, Nocardia sp. ALAA 2000, were found to be highly bioactive. It was isolated from the marine red alga Laurenica spectabilis collected off the Ras-Gharib coast of the Red Sea, Egypt. According to detailed identification studies, the strain was classified as a member of the genus Nocardia. The cultivation and chemical analysis of this species yielded four structurally related compounds namely, chrysophanol 8-methyl ether (1), asphodelin; 4,7'-bichrysophanol (2) and justicidin B (3), in addition to a novel bioactive compound ayamycin; 1,1-dichloro-4-ethyl-5-(4-nitro-phenyl)-hexan-2-one (4) which is unique in contain both chlorination and a rarely observed nitro group. The compounds were isolated by a series of chromatographic steps and their structures of 1 similar to 3 secured by detailed spectroscopic analysis of the MS and NMR data whereas that of 4 was elucidated by single crystal X-ray diffraction studies. These compounds displayed different potent antimicrobial activity against both Gram-positive and Gram-negative bacteria as well as fungi with MIC ranging from 0. 1 to 10 mu g/ml.

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