New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina
Authors
Robert A. Bara
Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr,
Geb.26.23. D-40225 Düsseldorf, Germany
Faculty of Fisheries and Marine Science, Sam Ratulangi University, Kampus Unsrat, Bahu Manado 95115, Indonesia
Author
Ilka Zerfaß
Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr,
Geb.26.23. D-40225 Düsseldorf, Germany
Author
Daowan Lai
Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr,
Geb.26.23. D-40225 Düsseldorf, Germany
Author
Weihan Lin
National Research Laboratories of Natural and Biomimetic Drugs, Peking University, Health Science Center,
100083 Beijing, People’s Republic of China
Author
Abdessamad Debbab
Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr,
Geb.26.23. D-40225 Düsseldorf, Germany
Author
Heike Brötz-Oesterelt
Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr,
Geb.26.23. D-40225 Düsseldorf, Germany
Author
Peter Proksch
Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr,
Geb.26.23. D-40225 Düsseldorf, Germany
Author
Chemical investigation of the endophytic fungus Botryosphaeria australis isolated from Avicennia marina originally from Hainan Province, P.R. China, yielded a new compound botryosphaenin (1), from the class of napthoquinone, together with 5 known compounds, botryosterpene (2) and 5-hydroxy-2,7-dimethoxynaphthalene-1,4-dione (3) and its derivatives, 6-ethyl-5-hydroxy-2,7-dimethoxynaphthalene-1,4-dione (4), O-methylaspmenone (5), O-methylasparvenone (6) and 5-(carboxymethyl)-7-hydroxy-1,4a-dimethyl-6-methylene decahydron aphthalene-1-carboxylic acid (7). Their structures were determined on the basis of spectroscopic methods including 1D (1H, 13C, and DEPT) and 2D (COSY, HMQC, HMBC, and ROESY) NMR experiments and by mass spectroscopic measurements The new compounds, 1 showed activity against the bacterial pathogens Staphylococcus aureus, several Streptococcus species and Bacillus subtilis, but also against the eukaryotic cell lines THP-1 (human leukemia monocyte) and BALB/3T3 (mouse embryonic fibroblast).