In vitro propagation of cryptocoryne ferruginea engler

Cryptocoryne ferruginea Engler (Araceae) is an endemic species of Borneo. Many Cryptocoryne species are popular as aquarium plants but there is limited information on the successful commercialization of the species from Malaysia. Surface sterilization using 70 % ethanol for 1 minute, 15 % (v/v) Cl...

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Main Author: Chen, Mei Yin
Format: Final Year Project Report
Language:English
English
Published: Universiti Malaysia Sarawak, (UNIMAS) 2012
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Online Access:http://ir.unimas.my/id/eprint/6194/1/IN%20VITRO%20PROPAGATION%20OF%20CRYPTOCORYNE%20FERRUGINEA%20ENGLER%2824pgs%29.pdf
http://ir.unimas.my/id/eprint/6194/8/IN%20VITRO%20PROPAGATION%20OF%20CRYPTOCORYNE%20FERRUGINEA%20ENGLER%28OCR%29.pdf
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Institution: Universiti Malaysia Sarawak
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spelling my.unimas.ir.61942023-01-31T08:59:21Z http://ir.unimas.my/id/eprint/6194/ In vitro propagation of cryptocoryne ferruginea engler Chen, Mei Yin Q Science (General) QL Zoology SB Plant culture Cryptocoryne ferruginea Engler (Araceae) is an endemic species of Borneo. Many Cryptocoryne species are popular as aquarium plants but there is limited information on the successful commercialization of the species from Malaysia. Surface sterilization using 70 % ethanol for 1 minute, 15 % (v/v) Clorox® for 15 minutes and rinsed thrice with distilled water produced the highest percentage of contamination-free petiole explants at 50 %. For runner explants, 15% (v/v) Clorox® for 12 minutes produced 58% contamination-free runner explants during the first two weeks after culture initiation in Murashige & Skoog (MS) medium. Only 4 explants (4.17 %) runner explants remained uncontaminated after four weeks. Incorporation of Plant Preservative Mixture (PPM™) into MS medium reduced contamination up to 100% in runner explants but only 5 explants (5.21%) were viable for shoot regeneration. The protocol requires further refinement to improve its efficiency. Multiple shoot, leaf and root regeneration used combinations of BAP (0-2.0 mg/L) with or without 0.1 mg/L IBA. Highest mean number of shoots (6.93) and leaves (3.33) per explant was observed in medium supplemented with 1.0mg/L BAP and 0.1mg/L IBA. Addition of 0.1mg/L IBA alone induced highest mean number of roots (2.93) per explant. Different medium (solid or liquid) with or without 0.1 mg/L NAA was used for root induction. Highest mean number of roots (4.25) per explant was induced in liquid medium supplemented with 0.1 mg/L NAA. Universiti Malaysia Sarawak, (UNIMAS) 2012 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/6194/1/IN%20VITRO%20PROPAGATION%20OF%20CRYPTOCORYNE%20FERRUGINEA%20ENGLER%2824pgs%29.pdf text en http://ir.unimas.my/id/eprint/6194/8/IN%20VITRO%20PROPAGATION%20OF%20CRYPTOCORYNE%20FERRUGINEA%20ENGLER%28OCR%29.pdf Chen, Mei Yin (2012) In vitro propagation of cryptocoryne ferruginea engler. [Final Year Project Report] (Unpublished)
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
English
topic Q Science (General)
QL Zoology
SB Plant culture
spellingShingle Q Science (General)
QL Zoology
SB Plant culture
Chen, Mei Yin
In vitro propagation of cryptocoryne ferruginea engler
description Cryptocoryne ferruginea Engler (Araceae) is an endemic species of Borneo. Many Cryptocoryne species are popular as aquarium plants but there is limited information on the successful commercialization of the species from Malaysia. Surface sterilization using 70 % ethanol for 1 minute, 15 % (v/v) Clorox® for 15 minutes and rinsed thrice with distilled water produced the highest percentage of contamination-free petiole explants at 50 %. For runner explants, 15% (v/v) Clorox® for 12 minutes produced 58% contamination-free runner explants during the first two weeks after culture initiation in Murashige & Skoog (MS) medium. Only 4 explants (4.17 %) runner explants remained uncontaminated after four weeks. Incorporation of Plant Preservative Mixture (PPM™) into MS medium reduced contamination up to 100% in runner explants but only 5 explants (5.21%) were viable for shoot regeneration. The protocol requires further refinement to improve its efficiency. Multiple shoot, leaf and root regeneration used combinations of BAP (0-2.0 mg/L) with or without 0.1 mg/L IBA. Highest mean number of shoots (6.93) and leaves (3.33) per explant was observed in medium supplemented with 1.0mg/L BAP and 0.1mg/L IBA. Addition of 0.1mg/L IBA alone induced highest mean number of roots (2.93) per explant. Different medium (solid or liquid) with or without 0.1 mg/L NAA was used for root induction. Highest mean number of roots (4.25) per explant was induced in liquid medium supplemented with 0.1 mg/L NAA.
format Final Year Project Report
author Chen, Mei Yin
author_facet Chen, Mei Yin
author_sort Chen, Mei Yin
title In vitro propagation of cryptocoryne ferruginea engler
title_short In vitro propagation of cryptocoryne ferruginea engler
title_full In vitro propagation of cryptocoryne ferruginea engler
title_fullStr In vitro propagation of cryptocoryne ferruginea engler
title_full_unstemmed In vitro propagation of cryptocoryne ferruginea engler
title_sort in vitro propagation of cryptocoryne ferruginea engler
publisher Universiti Malaysia Sarawak, (UNIMAS)
publishDate 2012
url http://ir.unimas.my/id/eprint/6194/1/IN%20VITRO%20PROPAGATION%20OF%20CRYPTOCORYNE%20FERRUGINEA%20ENGLER%2824pgs%29.pdf
http://ir.unimas.my/id/eprint/6194/8/IN%20VITRO%20PROPAGATION%20OF%20CRYPTOCORYNE%20FERRUGINEA%20ENGLER%28OCR%29.pdf
http://ir.unimas.my/id/eprint/6194/
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