Isolasi Metabolit Sekunder dari Jamur Endofitik Akar Tumbuhan Sambiloto (Andrographis paniculata Nees)
Main Authors: | Elfita, Elfita, Munawar, Munawar |
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Other Authors: | Raffiudin, Rika , Supena, Ence D J , Widyastuti, Utut , Purwantiningsih, Purwantiningsih, Sumaryada, Tony Ibnu , Sitanggang, Imas Sukaesih , Kusuma, Wisnu Ananta, Sulistyani, Sulistyani, Indahwati, Indahwati, Effendi, Sobri, Kusnanto, Ali |
Format: | BookSection PeerReviewed application/pdf |
Terbitan: |
FMIPA IPB Bagor
, 2014
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Subjects: | |
Online Access: |
http://eprints.unsri.ac.id/5880/1/PROSIDING_SEMIRATA_IPB.pdf http://eprints.unsri.ac.id/5880/ |
ctrlnum |
5880 |
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fullrecord |
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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"><title>Isolasi Metabolit Sekunder dari Jamur Endofitik Akar Tumbuhan Sambiloto (Andrographis paniculata Nees)</title><creator>Elfita, Elfita</creator><creator>Munawar, Munawar</creator><subject>QD Chemistry</subject><description>Endophytic fungi are important sources of bioactive natural products with enormous potential for the discovery of new molecules for drug discovery, industrial use and agricultural applications. This study was conducted on the isolation of secondary metabolite from the endophytic fungi of selected plants sambiloto. Three endophytic fungi from root of sambiloto were isolated and purified. One of the Unidentified fungi (Sb-1) was cultured in 5L Potato Dextrose Broth (PDB) medium at room temperature (no shaking) for 8 weeks. The culture broth was filtered to remove mycelia. The culture media was then extracted in 5 L ethyl acetate (2 times), followed by filtration and then taken to evaporation. The extract was separated into the fractions by column chromatography (CC) on silica gel. The fractions was further separated by silica gel column chromatography to give one aromatic compound. The molecular structure was identified on the basis of spectroscopic UV analysis</description><publisher>FMIPA IPB Bagor</publisher><contributor>Raffiudin, Rika </contributor><contributor>Supena, Ence D J </contributor><contributor>Widyastuti, Utut </contributor><contributor>Purwantiningsih, Purwantiningsih</contributor><contributor>Sumaryada, Tony Ibnu </contributor><contributor>Sitanggang, Imas Sukaesih </contributor><contributor>Kusuma, Wisnu Ananta</contributor><contributor>Sulistyani, Sulistyani</contributor><contributor>Indahwati, Indahwati</contributor><contributor>Effendi, Sobri</contributor><contributor>Kusnanto, Ali </contributor><date>2014-05-09</date><type>Book:BookSection</type><type>PeerReview:PeerReviewed</type><type>File:application/pdf</type><identifier>http://eprints.unsri.ac.id/5880/1/PROSIDING_SEMIRATA_IPB.pdf</identifier><identifier>Elfita, Elfita and Munawar, Munawar (2014) Isolasi Metabolit Sekunder dari Jamur Endofitik Akar Tumbuhan Sambiloto (Andrographis paniculata Nees). In: Prosiding Seminar Nasional dan Rapat Tahunan Bidang MIPA 2014. FMIPA IPB Bagor, Bogor, pp. 2-7. ISBN 978-602-70491-0-9</identifier><relation>http://eprints.unsri.ac.id/5880/</relation><recordID>5880</recordID></dc>
|
format |
Book:BookSection Book PeerReview:PeerReviewed PeerReview File:application/pdf File |
author |
Elfita, Elfita Munawar, Munawar |
author2 |
Raffiudin, Rika Supena, Ence D J Widyastuti, Utut Purwantiningsih, Purwantiningsih Sumaryada, Tony Ibnu Sitanggang, Imas Sukaesih Kusuma, Wisnu Ananta Sulistyani, Sulistyani Indahwati, Indahwati Effendi, Sobri Kusnanto, Ali |
title |
Isolasi Metabolit Sekunder dari Jamur Endofitik Akar Tumbuhan Sambiloto (Andrographis paniculata Nees) |
publisher |
FMIPA IPB Bagor |
publishDate |
2014 |
isbn |
9786027049109 |
topic |
QD Chemistry |
url |
http://eprints.unsri.ac.id/5880/1/PROSIDING_SEMIRATA_IPB.pdf http://eprints.unsri.ac.id/5880/ |
contents |
Endophytic fungi are important sources of bioactive natural products with enormous potential for the discovery of new molecules for drug discovery, industrial use and agricultural applications. This study was conducted on the isolation of secondary metabolite from the endophytic fungi of selected plants sambiloto. Three endophytic fungi from root of sambiloto were isolated and purified. One of the Unidentified fungi (Sb-1) was cultured in 5L Potato Dextrose Broth (PDB) medium at room temperature (no shaking) for 8 weeks. The culture broth was filtered to remove mycelia. The culture media was then extracted in 5 L ethyl acetate (2 times), followed by filtration and then taken to evaporation. The extract was separated into the fractions by column chromatography (CC) on silica gel. The fractions was further separated by silica gel column chromatography to give one aromatic compound. The molecular structure was identified on the basis of spectroscopic UV analysis |
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KOTA PALEMBANG |
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SUMATERA SELATAN |
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