In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram

Curcuma mangga Val., commonly known as the mango ginger has been used traditionally as a seasoning for food and as a treatment for stomach aches, fever, and cancer. Due to its medicinal importance, a systematic approach was taken to establish a rapidly growing suspension culture of C. mangga. In ini...

Full description

Bibliographic Details
Main Author: Meenakshi Sundram, Tamil Chelvan
Format: Thesis
Published: 2012
Subjects:
Online Access:http://pendeta.um.edu.my/client/default/search/results?qu=In+vitro+cultures+of+Curcuma+mangga+Val.+for+the+production&te=
http://studentsrepo.um.edu.my/3802/1/1._Title_page%2C_abstract%2C_content.pdf
http://studentsrepo.um.edu.my/3802/2/2._orginal_literacy_declaration.pdf
http://studentsrepo.um.edu.my/3802/3/3._FULL_THESIS_final.pdf
http://studentsrepo.um.edu.my/3802/4/4._PUBLICATION%2D_APPENDIX.pdf
http://studentsrepo.um.edu.my/3802/5/FRONT_COVER_PAGE.pdf
_version_ 1848772499849871360
author Meenakshi Sundram, Tamil Chelvan
author_facet Meenakshi Sundram, Tamil Chelvan
author_sort Meenakshi Sundram, Tamil Chelvan
building UM Research Repository
collection Online Access
description Curcuma mangga Val., commonly known as the mango ginger has been used traditionally as a seasoning for food and as a treatment for stomach aches, fever, and cancer. Due to its medicinal importance, a systematic approach was taken to establish a rapidly growing suspension culture of C. mangga. In initiating callus, various responses were obtained from shoot bud explants cultured on MS basal medium supplemented with different concentrations of 2,4-D, NAA and IAA either alone or in combinations. Different concentrations of sucrose were also tested. Rapid growing friable callusobtained from shoot explants cultured on MS basal medium supplemented with 1 mg l-1 2,4-D, 30 g l-1 sucrose and 2 g l-1 gelrite were selected for the initiation of suspension cultures based on histological morphology. From various medium screened, rapid growing suspension cultures were established by using MS liquid medium supplemented with 0.3 mg l-1 2,4-D, 0.1 mg l-1 NAA, 30 g l-1 sucrose, 0.1 g l-1 malt extract, 0.5 mg l-1 d-Biotin, 100 mg l-1 glutamine, 5 mg l-1 ascorbic acid and citric acid respectively. Phenolic compounds production was most effectively controlled by the incorporation of ascorbic and citric acid as antioxidants. (E)-labda-8(17),12-dien-15,16 dial is one of the bioactive compounds isolated from rhizomes of C. mangga. Recently, the cytotoxicity of this compound against cancer cells has been reported. (E)-Labda-8(17),12-dien-15,16 dial was extracted from cells, callus, rhizomes and shoots using solvent extraction method. Gas Chromatography (GC) and Gas Chromatography Flame Ionization Detector (GCFID) was used to compare the quantity of (E)-labda-8(17),12-dien-15,16 dial production in suspension cells and callus induced through various treatment and at different growth period.The presence of this compound in field grown rhizomes and in vivo shoot buds samples were also tested. The amount of (E)-labda-8(17),12-dien-15,16 dial in in vivo sources was higher than the in vitro sources, but the presence can be enhanced through various method in future studies.
first_indexed 2025-11-14T13:27:29Z
format Thesis
id um-3802
institution University Malaya
institution_category Local University
last_indexed 2025-11-14T13:27:29Z
publishDate 2012
recordtype eprints
repository_type Digital Repository
spelling um-38022013-08-30T04:19:19Z In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram Meenakshi Sundram, Tamil Chelvan QH301 Biology Curcuma mangga Val., commonly known as the mango ginger has been used traditionally as a seasoning for food and as a treatment for stomach aches, fever, and cancer. Due to its medicinal importance, a systematic approach was taken to establish a rapidly growing suspension culture of C. mangga. In initiating callus, various responses were obtained from shoot bud explants cultured on MS basal medium supplemented with different concentrations of 2,4-D, NAA and IAA either alone or in combinations. Different concentrations of sucrose were also tested. Rapid growing friable callusobtained from shoot explants cultured on MS basal medium supplemented with 1 mg l-1 2,4-D, 30 g l-1 sucrose and 2 g l-1 gelrite were selected for the initiation of suspension cultures based on histological morphology. From various medium screened, rapid growing suspension cultures were established by using MS liquid medium supplemented with 0.3 mg l-1 2,4-D, 0.1 mg l-1 NAA, 30 g l-1 sucrose, 0.1 g l-1 malt extract, 0.5 mg l-1 d-Biotin, 100 mg l-1 glutamine, 5 mg l-1 ascorbic acid and citric acid respectively. Phenolic compounds production was most effectively controlled by the incorporation of ascorbic and citric acid as antioxidants. (E)-labda-8(17),12-dien-15,16 dial is one of the bioactive compounds isolated from rhizomes of C. mangga. Recently, the cytotoxicity of this compound against cancer cells has been reported. (E)-Labda-8(17),12-dien-15,16 dial was extracted from cells, callus, rhizomes and shoots using solvent extraction method. Gas Chromatography (GC) and Gas Chromatography Flame Ionization Detector (GCFID) was used to compare the quantity of (E)-labda-8(17),12-dien-15,16 dial production in suspension cells and callus induced through various treatment and at different growth period.The presence of this compound in field grown rhizomes and in vivo shoot buds samples were also tested. The amount of (E)-labda-8(17),12-dien-15,16 dial in in vivo sources was higher than the in vitro sources, but the presence can be enhanced through various method in future studies. 2012 Thesis NonPeerReviewed application/pdf http://studentsrepo.um.edu.my/3802/1/1._Title_page%2C_abstract%2C_content.pdf application/pdf http://studentsrepo.um.edu.my/3802/2/2._orginal_literacy_declaration.pdf application/pdf http://studentsrepo.um.edu.my/3802/3/3._FULL_THESIS_final.pdf application/pdf http://studentsrepo.um.edu.my/3802/4/4._PUBLICATION%2D_APPENDIX.pdf application/pdf http://studentsrepo.um.edu.my/3802/5/FRONT_COVER_PAGE.pdf http://pendeta.um.edu.my/client/default/search/results?qu=In+vitro+cultures+of+Curcuma+mangga+Val.+for+the+production&te= Meenakshi Sundram, Tamil Chelvan (2012) In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram. Masters thesis, University of Malaya. http://studentsrepo.um.edu.my/3802/
spellingShingle QH301 Biology
Meenakshi Sundram, Tamil Chelvan
In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram
title In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram
title_full In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram
title_fullStr In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram
title_full_unstemmed In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram
title_short In vitro cultures of Curcuma mangga Val. for the production of (E)-labda-8(17), 12-diene-15, 16-dial / Tamil Chelvan Meenakshi Sundram
title_sort in vitro cultures of curcuma mangga val. for the production of (e)-labda-8(17), 12-diene-15, 16-dial / tamil chelvan meenakshi sundram
topic QH301 Biology
url http://pendeta.um.edu.my/client/default/search/results?qu=In+vitro+cultures+of+Curcuma+mangga+Val.+for+the+production&te=
http://pendeta.um.edu.my/client/default/search/results?qu=In+vitro+cultures+of+Curcuma+mangga+Val.+for+the+production&te=
http://studentsrepo.um.edu.my/3802/1/1._Title_page%2C_abstract%2C_content.pdf
http://studentsrepo.um.edu.my/3802/2/2._orginal_literacy_declaration.pdf
http://studentsrepo.um.edu.my/3802/3/3._FULL_THESIS_final.pdf
http://studentsrepo.um.edu.my/3802/4/4._PUBLICATION%2D_APPENDIX.pdf
http://studentsrepo.um.edu.my/3802/5/FRONT_COVER_PAGE.pdf