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
  • Ilka Zerfaß Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, Germany
  • Daowan Lai Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, Germany
  • Weihan Lin National Research Laboratories of Natural and Biomimetic Drugs, Peking University, Health Science Center, 100083 Beijing, People’s Republic of China
  • Abdessamad Debbab Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, Germany
  • Heike Brötz-Oesterelt Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, Germany
  • Peter Proksch Institut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, Germany

DOI:

https://doi.org/10.15578/squalen.86

Keywords:

Mangrove, Avicennia marina, Botryosphaeria australis, antibiotic activities, cytotoxicity

Abstract

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).

Downloads

Published

2013-12-12