Subscribe to RSS
DOI: 10.1055/s-2007-967131
© Georg Thieme Verlag KG Stuttgart · New York
Two New Depsipeptides from the Marine Fungus Spicellum roseum
Publication History
Received: October 30, 2006
Accepted: January 31, 2007
Publication Date:
12 March 2007 (online)
![](https://www.thieme-connect.de/media/plantamedica/200704/lookinside/thumbnails/10.1055-s-2007-967131-1.jpg)
Abstract
Investigation of the secondary metabolites of the marine-derived fungus Spicellum roseum yielded two new cyclohexadepsipeptides, spicellamide A (1) and spicellamide B (2). The structures of 1 and 2 were determined based on extensive evaluations of NMR and MS data. The absolute configuration was deduced after hydrolysis using Marfey's method, chiral chromatography, as well as NOESY and modeling data.
Key words
Spicellum roseum - marine-derived fungi - endophyte - Ectyplasia perox - depsipeptide
- Supporting Information for this article is available online at
- Supporting Information .
References
- 1 Bhadury P, Mohammad B T, Wright P C. The current status of natural products from marine fungi and their potential as anti-infective agents. J Ind Microbiol Biotechnol. 2006; 33 325-37.
- 2 Carlo L, Fornelli F, Ramires R, Nenna S, Tursi A, Caiaffa M F. et al . Cytotoxic effects of the mycotoxin beauvericin to human cell lines of myeloid origin. Pharmacol Res. 2004; 49 73-7.
- 3 Dobler M, Dunitz J D, Krajewski J. Structure of the K+ complex with enniatin B, a macrocyclic antibiotic with K+ transport properties. J Mol Biol. 1969; 28 603-6.
- 4 Gupta S, Krasnoff S B, Underwood N L, Renwick J AA, Roberts D W. Isolation of beauvericin as an insect toxin from Fusarium semitectum and Fusarium moniliforme var. subglutinans . Mycopathologia. 1991; 115 185-9.
- 5 Tomoda H, Huang X H, Cao J, Nishida H, Nagao R, Okuda S. et al . Inhibition of acyl-CoA: cholesterol acyltransferase activity by cyclodepsipeptide antibiotics. J Antibiot. 1992; 45 1626-32.
- 6 Krohn K, Steingröver K, Aust H J, Draeger S, Schulz B. Biologically active metabolites from fungi, 17. 8-α-acetoxyverrol, a new member of the trichothecene sesquiterpenes. Nat Prod Res. 2003; 17 67-70.
- 7 Tanaka K, Plattner R D, Yamagishi R, Minamisawa M, Manabe M, Kawasugi S. et al . 8-Deoxy-trichothecin production by Spicellum roseum isolated from a cultivated mushroom in Japan. Mycotoxins. 2001; 51 1-7.
- 8 Höller U, Wright A D, Matthée G F, König G M, Draeger S, Aust H J. et al . Fungi from marine sponges: diversity, biological activity and secondary metabolites. Mycol Res. 2000; 11 1354-65.
- 9 Schulz B, Sucker J, Aust H J, Krohn K, Ludewig K, Jones P G. et al . Biologically active secondary metabolites of endophytic Pezicula species. Mycol Res. 1995; 99 1007-15.
- 10 Luesch H, Yoshida W Y, Moore R E, Paul V J, Mooberry S L. Isolation, structure determination, and biological activity of lyngbyabellin A from the marine cyanobacterium Lyngbya majuscula . J Nat Prod. 2000; 63 611-5.
Prof. Dr. Gabriele M. König
Institute for Pharmaceutical Biology
University of Bonn
Nussallee 6
53115 Bonn
Germany
Phone: +49-228-733-747
Fax: +49-228-733-250
Email: G.Koenig@uni-bonn.de
- www.thieme-connect.de/ejournals/toc/plantamedica