Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata

Endophytic fungi has an economic potential as raw material for biologically active compounds. Cladosporium oxysporum is one of the endophytic fungi isolated from Indonesian medicinal plant Aglaia odorata Lour (Local name: Pacarcina). This planth has been used for fever, cough, diarrhea, inflammation...

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Main Authors: Armila Fatma Setyaningrum, Risma Pratiwi, Suciati, Noor Erma Nasution, Gunawan Indrayanto
Format: Article PeerReviewed
Language:English
English
English
Published: Universitas Sebelas Maret 2018
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Online Access:http://repository.unair.ac.id/93622/1/C-15%20Artikel.pdf
http://repository.unair.ac.id/93622/3/C-15%20Reviewer.pdf
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http://repository.unair.ac.id/93622/
https://jurnal.uns.ac.id/alchemy/article/view/12974
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spelling id-langga.936222020-02-04T07:48:53Z http://repository.unair.ac.id/93622/ Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata Armila Fatma Setyaningrum Risma Pratiwi Suciati Noor Erma Nasution Gunawan Indrayanto R Medicine RS Pharmacy and materia medica Endophytic fungi has an economic potential as raw material for biologically active compounds. Cladosporium oxysporum is one of the endophytic fungi isolated from Indonesian medicinal plant Aglaia odorata Lour (Local name: Pacarcina). This planth has been used for fever, cough, diarrhea, inflammation and injury. In our previous study, the ethyl acetate extract and several fractions of the extract of C. oxysporum showed antimicrobial activity against Candida albicans, Escherichia coli, and Staphylococcus aureus. The objective of the currents study is to investigate the chemical constituent of the active fraction. Purification of the metabolite was achieved by using column chromatography followed by preparative thin layer chromatography. Identification of the metabolite was conducted by using TLC densitometry, GC-FID and GCMS. Compound 1 was isolated from fraction 12. The purity of this compound was determined by 2D-TLC and GC-FID. The UV-Vis profile of compound 1 indicates a phenolic compound. Further analysis by using GCMS shows one peak at a retention time (Rt) of 23.80 minutes, predicted as 4-4’-(1-methylethylidene)-bisphenol. The chemical constituent of the sub fraction 12.2.7 (fraction a) is identified as 4-4’-(1-methylethylidene)-bisphenol. Universitas Sebelas Maret 2018-09-03 Article PeerReviewed text en http://repository.unair.ac.id/93622/1/C-15%20Artikel.pdf text en http://repository.unair.ac.id/93622/3/C-15%20Reviewer.pdf text en http://repository.unair.ac.id/93622/2/C-15%20Result.pdf Armila Fatma Setyaningrum and Risma Pratiwi and Suciati and Noor Erma Nasution and Gunawan Indrayanto (2018) Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata. Alchemy Jurnal Penelitian Kimia, 14 (2). pp. 193-201. ISSN 1412-4092 https://jurnal.uns.ac.id/alchemy/article/view/12974 doi.org/10.20961/alchemy.14.2.12974.193-201
institution Universitas Airlangga
building Universitas Airlangga Library
country Indonesia
collection UNAIR Repository
language English
English
English
topic R Medicine
RS Pharmacy and materia medica
spellingShingle R Medicine
RS Pharmacy and materia medica
Armila Fatma Setyaningrum
Risma Pratiwi
Suciati
Noor Erma Nasution
Gunawan Indrayanto
Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata
description Endophytic fungi has an economic potential as raw material for biologically active compounds. Cladosporium oxysporum is one of the endophytic fungi isolated from Indonesian medicinal plant Aglaia odorata Lour (Local name: Pacarcina). This planth has been used for fever, cough, diarrhea, inflammation and injury. In our previous study, the ethyl acetate extract and several fractions of the extract of C. oxysporum showed antimicrobial activity against Candida albicans, Escherichia coli, and Staphylococcus aureus. The objective of the currents study is to investigate the chemical constituent of the active fraction. Purification of the metabolite was achieved by using column chromatography followed by preparative thin layer chromatography. Identification of the metabolite was conducted by using TLC densitometry, GC-FID and GCMS. Compound 1 was isolated from fraction 12. The purity of this compound was determined by 2D-TLC and GC-FID. The UV-Vis profile of compound 1 indicates a phenolic compound. Further analysis by using GCMS shows one peak at a retention time (Rt) of 23.80 minutes, predicted as 4-4’-(1-methylethylidene)-bisphenol. The chemical constituent of the sub fraction 12.2.7 (fraction a) is identified as 4-4’-(1-methylethylidene)-bisphenol.
format Article
PeerReviewed
author Armila Fatma Setyaningrum
Risma Pratiwi
Suciati
Noor Erma Nasution
Gunawan Indrayanto
author_facet Armila Fatma Setyaningrum
Risma Pratiwi
Suciati
Noor Erma Nasution
Gunawan Indrayanto
author_sort Armila Fatma Setyaningrum
title Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata
title_short Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata
title_full Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata
title_fullStr Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata
title_full_unstemmed Identification of 4-4’-(1-methylethylidene)-bisphenol from an Endophytic Fungus Cladosporium oxysporum derived from Aglaia odorata
title_sort identification of 4-4’-(1-methylethylidene)-bisphenol from an endophytic fungus cladosporium oxysporum derived from aglaia odorata
publisher Universitas Sebelas Maret
publishDate 2018
url http://repository.unair.ac.id/93622/1/C-15%20Artikel.pdf
http://repository.unair.ac.id/93622/3/C-15%20Reviewer.pdf
http://repository.unair.ac.id/93622/2/C-15%20Result.pdf
http://repository.unair.ac.id/93622/
https://jurnal.uns.ac.id/alchemy/article/view/12974
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