New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina

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-dimet...

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Main Authors: Robert A. Bara, Ilka Zerfaß, Daowan Lai, Weihan Lin, Abdessamad Debbab, Heike Brötz-Oesterelt, Peter Proksch
Format: Article
Language:English
Published: Kementerian Kelautan dan Perikanan 2013-12-01
Series:Squalen
Subjects:
Online Access:http://bbp4b.litbang.kkp.go.id/squalen-bulletin/index.php/squalen/article/view/86
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author Robert A. Bara
Ilka Zerfaß
Daowan Lai
Weihan Lin
Abdessamad Debbab
Heike Brötz-Oesterelt
Peter Proksch
author_facet Robert A. Bara
Ilka Zerfaß
Daowan Lai
Weihan Lin
Abdessamad Debbab
Heike Brötz-Oesterelt
Peter Proksch
author_sort Robert A. Bara
collection DOAJ
description 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).
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spelling doaj.art-2efead30226246d3b051f9bf8fed61db2022-12-22T03:14:06ZengKementerian Kelautan dan PerikananSqualen2089-56902406-92722013-12-018313914510.15578/squalen.v8i3.8663New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marinaRobert A. Bara0Ilka Zerfaß1Daowan Lai2Weihan Lin3Abdessamad Debbab4Heike Brötz-Oesterelt5Peter Proksch6Institut 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, IndonesiaInstitut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, GermanyInstitut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, GermanyNational Research Laboratories of Natural and Biomimetic Drugs, Peking University, Health Science Center, 100083 Beijing, People’s Republic of ChinaInstitut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, GermanyInstitut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, GermanyInstitut für Pharmazeutische Biologie und Biotechnologie Heinrich-Heine-Universität Düsseldorf Universitätsstr, Geb.26.23. D-40225 Düsseldorf, GermanyChemical 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).http://bbp4b.litbang.kkp.go.id/squalen-bulletin/index.php/squalen/article/view/86MangroveAvicennia marinaBotryosphaeria australisantibiotic activitiescytotoxicity
spellingShingle Robert A. Bara
Ilka Zerfaß
Daowan Lai
Weihan Lin
Abdessamad Debbab
Heike Brötz-Oesterelt
Peter Proksch
New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina
Squalen
Mangrove
Avicennia marina
Botryosphaeria australis
antibiotic activities
cytotoxicity
title New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina
title_full New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina
title_fullStr New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina
title_full_unstemmed New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina
title_short New Natural Product from Botryosphaeria australis, an Endophyte from Mangrove Avicennia marina
title_sort new natural product from botryosphaeria australis an endophyte from mangrove avicennia marina
topic Mangrove
Avicennia marina
Botryosphaeria australis
antibiotic activities
cytotoxicity
url http://bbp4b.litbang.kkp.go.id/squalen-bulletin/index.php/squalen/article/view/86
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