ELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE

Aquilaria malaccensis is a common agarwood-producing tree cultivated in Indonesia. The agarwood can be induced by biological agents such as Fusarium solani and chemical ones, such as methyl jasmonate (MeJA). In vitro culture using A. malaccensis calli and F. solani Gorontalo strain (GSL1) ,Jambi str...

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Main Author: Puji Utami, Nadia
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/37127
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:37127
spelling id-itb.:371272019-03-18T16:20:44ZELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE Puji Utami, Nadia Indonesia Final Project Aquilaria malaccensis, Elicitation, Agarwood, Calli, Chromone INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/37127 Aquilaria malaccensis is a common agarwood-producing tree cultivated in Indonesia. The agarwood can be induced by biological agents such as Fusarium solani and chemical ones, such as methyl jasmonate (MeJA). In vitro culture using A. malaccensis calli and F. solani Gorontalo strain (GSL1) ,Jambi strain (GSL2), and methyl jasmonate, as inducer secondary metabolite production, can be used as an alternative methode to study the formation of agarwood compounds. Thus, this study aims to observe the effect of elicitation by F. solani GSL1 and GSL2 strains, and methyl jasmonate on the growth and secondary metabolite production in A. malaccensis calli. The study began by conducting calli propagation on Murashige-Skoog (MS) medium with the addition of 2 ppm 2,4-D (2,4-Dichlorophenoxyacetic acid) and 0,1 ppm (6-Benzylaminopurine) BAP. The calli was subcultured to another medium containing extract from GSL1 8 mg /L, GSL2 8 mg/L, and MeJA 100 ?M, then incubated for 20 days in dark and room temperature. The calli were measured to determine growth rate and cell viability, and subjected to testing by GC-MS to determine the profile of secondary metabolites present. The results showed that the treatments with GSL1, GSL2, and MeJA did not significantly influence calli growth rate, but decreased cell viability in the GSL1 (24,12%), GSL2 (17,04%), and MeJA (33,21%) treatments. The results of the GC-MS analysis showed that typical agarwood compounds, chromone (6-methoxy-2- (4-methoxyphenetyl) -4H-chromen-4-on), were detected in the calli of the GSL2 (5,72%) and MeJA (11,16%) treatments. From the study of this study it can be concluded that MeJA is the best elicitor in inducing agarwood compounds in A. malaccensis calli. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Aquilaria malaccensis is a common agarwood-producing tree cultivated in Indonesia. The agarwood can be induced by biological agents such as Fusarium solani and chemical ones, such as methyl jasmonate (MeJA). In vitro culture using A. malaccensis calli and F. solani Gorontalo strain (GSL1) ,Jambi strain (GSL2), and methyl jasmonate, as inducer secondary metabolite production, can be used as an alternative methode to study the formation of agarwood compounds. Thus, this study aims to observe the effect of elicitation by F. solani GSL1 and GSL2 strains, and methyl jasmonate on the growth and secondary metabolite production in A. malaccensis calli. The study began by conducting calli propagation on Murashige-Skoog (MS) medium with the addition of 2 ppm 2,4-D (2,4-Dichlorophenoxyacetic acid) and 0,1 ppm (6-Benzylaminopurine) BAP. The calli was subcultured to another medium containing extract from GSL1 8 mg /L, GSL2 8 mg/L, and MeJA 100 ?M, then incubated for 20 days in dark and room temperature. The calli were measured to determine growth rate and cell viability, and subjected to testing by GC-MS to determine the profile of secondary metabolites present. The results showed that the treatments with GSL1, GSL2, and MeJA did not significantly influence calli growth rate, but decreased cell viability in the GSL1 (24,12%), GSL2 (17,04%), and MeJA (33,21%) treatments. The results of the GC-MS analysis showed that typical agarwood compounds, chromone (6-methoxy-2- (4-methoxyphenetyl) -4H-chromen-4-on), were detected in the calli of the GSL2 (5,72%) and MeJA (11,16%) treatments. From the study of this study it can be concluded that MeJA is the best elicitor in inducing agarwood compounds in A. malaccensis calli.
format Final Project
author Puji Utami, Nadia
spellingShingle Puji Utami, Nadia
ELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE
author_facet Puji Utami, Nadia
author_sort Puji Utami, Nadia
title ELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE
title_short ELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE
title_full ELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE
title_fullStr ELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE
title_full_unstemmed ELICITATION OF SECONDARY METABOLITES IN AGARWOOD CALLI (AQUILARIA MALACCENSIS LAMK.) BY FUSARIUM SOLANI MYCELIUM EXTRACT AND METHYL JASMONATE
title_sort elicitation of secondary metabolites in agarwood calli (aquilaria malaccensis lamk.) by fusarium solani mycelium extract and methyl jasmonate
url https://digilib.itb.ac.id/gdl/view/37127
_version_ 1822924820918042624