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Title: | Biotransformation of α-mangostin by Colletotrichum sp. MT02 and Phomopsis euphorbiae K12 |
Authors: | Arunrattiyakorn P. Suwannasai N. Aree T. Kanokmedhakul S. Ito H. Kanzaki H. |
Keywords: | Bioconversion Biomolecules Cell culture Spectroscopic analysis X ray crystallography Antimycobacterial activity Biotransformation Colletotrichum sp Microbial transformation Mycobacterium tuberculosis Phomopsis Prenylated xanthone X-ray crystallographic analysis Metabolites 12,13,19 trihydroxymangostin 12,13,20 trihydroxymangostin 17,18 dihydroxymangostanin 20 hydroxymangostanin alpha mangostin antiinfective agent cyclomangostanin doxorubicin tamoxifen unclassified drug xanthone derivative antimicrobial activity article biotransformation carbon nuclear magnetic resonance Colletotrichum cytotoxicity enzyme structure enzyme substrate enzyme synthesis fungal strain fungus fungus isolation Garcinia mangostana IC 50 incubation time nonhuman nucleotide sequence olive tree Phomopsis euphorbiae proton nuclear magnetic resonance X ray crystallography |
Issue Date: | 2014 |
Abstract: | The microbial transformation of the major mangosteen pericarp xanthone, α-mangostin (1) by the endophytic fungi Colletotrichum sp. MT02 and Phomopsis euphorbiae K12 resulted in the production of the five metabolites 2-6. Biotransformation with Colletotrichum sp. MT02 converted 1 into 17,18-dihydroxymangostanin (2) and cyclomangostanin (3), while incubation with P. euphorbiae K12 gave 12,13,20-trihydroxymangostin (4), 12,13,19- trihydroxymangostin (5), and 20-hydroxymangostanin (6) as transformation products. The structures of these metabolites were elucidated via spectroscopic analyses, and for compound 3, the structure was confirmed by X-ray crystallographic analysis. All metabolites are new, and metabolite 3 possessed an unusual structure of bis-ring fused xanthene in nature. In addition, substrate and all products were evaluated for the antimycobacterial activity against Mycobacterium tuberculosis as well as the cytotoxicity against breast cancer (MCF-7) cell lines. © 2014 Elsevier B.V. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13798 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84896280271&doi=10.1016%2fj.molcatb.2014.02.010&partnerID=40&md5=a30cd03964204fad2d898a40f5a87983 |
ISSN: | 13811177 |
Appears in Collections: | Scopus 1983-2021 |
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