New Pyran of An Endophytic Fungus Fusarium sp. Isolated from The Leaves of Brotowali (Tinaspora Crispa)
| Main Authors: | Elfita, Elfita, Muharni, Muharni, Munawar, Munawar, Suprayetno, Suprayetno |
|---|---|
| Format: | Article PeerReviewed Book |
| Bahasa: | eng |
| Terbitan: |
Department of Chemistry, Universitas Gadjah Mada
, 2013
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| Subjects: | |
| Online Access: |
http://repository.unsri.ac.id/24264/1/IJC_2013_Elfita_%2812%29.pdf http://repository.unsri.ac.id/24264/ |
| ctrlnum |
24264 |
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<dc schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><relation>http://repository.unsri.ac.id/24264/</relation><title>New Pyran of An Endophytic Fungus Fusarium sp. Isolated from The Leaves of Brotowali (Tinaspora Crispa)</title><creator>Elfita, Elfita</creator><creator>Muharni, Muharni</creator><creator>Munawar, Munawar</creator><creator>Suprayetno, Suprayetno</creator><subject>QD1-999 Chemistry</subject><description>Endophytes are microorganisms that reside asymptomatically in the tissues of higher plants and are relatively unstudied and a promising source of novel organic natural metabolites exhibiting a variety of biological activities. As a part of our systematic search for new bioactive lead structures from endophytic, the endophytic fungus Fusarium sp. isolated from the leaves of Brotowali (Tinaspora crispa), was cultured for isolation of metabolite. The endophytic fungus was cultivated on 6 L of Potatos Dextose Broth (PDB) medium at room temperature (no shaking) for 8 weeks. The cultures were then extracted with ethyl acetate to afford 9.4 g of residue after removal of the solvent under reduced pressure. The extract was separated into the fractions by column chromatography (CC) on silica gel. The fractions were further separated by silica gel column chromatography to give one compound. The molecular structure was established on the basis of spectroscopic analysis including UV, IR, 1H-NMR, 13C-NMR, HMQC, HMBC, COSY, and MS. The compound was determined as a new pyran.</description><publisher>Department of Chemistry, Universitas Gadjah Mada</publisher><date>2013-11</date><type>Journal:Article</type><type>PeerReview:PeerReviewed</type><type>Book:Book</type><language>eng</language><identifier>http://repository.unsri.ac.id/24264/1/IJC_2013_Elfita_%2812%29.pdf</identifier><identifier> Elfita, Elfita and Muharni, Muharni and Munawar, Munawar and Suprayetno, Suprayetno (2013) New Pyran of An Endophytic Fungus Fusarium sp. Isolated from The Leaves of Brotowali (Tinaspora Crispa). Journal of Chemistry, 13 (3). pp. 209-215. ISSN 1411-9420 </identifier><recordID>24264</recordID></dc>
|
| language |
eng |
| format |
Journal:Article Journal PeerReview:PeerReviewed PeerReview Book:Book Book |
| author |
Elfita, Elfita Muharni, Muharni Munawar, Munawar Suprayetno, Suprayetno |
| title |
New Pyran of An Endophytic Fungus Fusarium sp. Isolated from The Leaves of Brotowali (Tinaspora Crispa) |
| publisher |
Department of Chemistry, Universitas Gadjah Mada |
| publishDate |
2013 |
| topic |
QD1-999 Chemistry |
| url |
http://repository.unsri.ac.id/24264/1/IJC_2013_Elfita_%2812%29.pdf http://repository.unsri.ac.id/24264/ |
| contents |
Endophytes are microorganisms that reside asymptomatically in the tissues of higher plants and are relatively unstudied and a promising source of novel organic natural metabolites exhibiting a variety of biological activities. As a part of our systematic search for new bioactive lead structures from endophytic, the endophytic fungus Fusarium sp. isolated from the leaves of Brotowali (Tinaspora crispa), was cultured for isolation of metabolite. The endophytic fungus was cultivated on 6 L of Potatos Dextose Broth (PDB) medium at room temperature (no shaking) for 8 weeks. The cultures were then extracted with ethyl acetate to afford 9.4 g of residue after removal of the solvent under reduced pressure. The extract was separated into the fractions by column chromatography (CC) on silica gel. The fractions were further separated by silica gel column chromatography to give one compound. The molecular structure was established on the basis of spectroscopic analysis including UV, IR, 1H-NMR, 13C-NMR, HMQC, HMBC, COSY, and MS. The compound was determined as a new pyran. |
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