Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq.

Shorea leprosula Miq., a fast growing dipterocarps, has potential for reforestation of degraded forest. However, planting stock of this species is scarce because fruiting is irregular and the seeds are recalcitrant. Micropropagation has been considered as an alternative to mass produce the planting...

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Main Author: Liu, Yan Tin
Format: Final Year Project Report
Language:English
English
Published: unimas 2009
Subjects:
Online Access:http://ir.unimas.my/id/eprint/20801/1/Establishment%20of%20contamination-free%2024pgs.pdf
http://ir.unimas.my/id/eprint/20801/8/Liu%20Yan%20ft.pdf
http://ir.unimas.my/id/eprint/20801/
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spelling my.unimas.ir.208012024-06-13T08:21:00Z http://ir.unimas.my/id/eprint/20801/ Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq. Liu, Yan Tin Q Science (General) QR Microbiology Shorea leprosula Miq., a fast growing dipterocarps, has potential for reforestation of degraded forest. However, planting stock of this species is scarce because fruiting is irregular and the seeds are recalcitrant. Micropropagation has been considered as an alternative to mass produce the planting stock. The objective of this study was to develop an effective surface sterilization protocol to establish contamination-free culture as the first step towards development of micropropagation of S. leprosula. The surface sterilization protocol developed so far started with soaking the fieldderived shoot-tip and nodal explants in a fungicide solution for one and three hours respectively. The explants were then dipped in 75% ethanol for one minute and surface sterilized in 5% Clorox added with Tween 20 for 10 minutes and Chlorine Dioxide at 50 ppm for 10 minutes. The explants were then rinsed with autoclaved-RO water for at least three times. Nodal explants were pulse-treated with 10 ml/L PPM for overnight whereas shoot-tip explants were pulsedtreated with PPM at 5 ml/L for an hour. Surface-sterilized explants were trimmed and cultured on MS basal medium supplemented with 20 g/L sucrose. BAP and TDZ were found to be effective in inducing new buds growth on nodal explants. Nodal explants inoculated on MS basal medium supplemented with 2 mg/L BAP and 0.1 mg/L NAA showed new buds growth. unimas 2009 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/20801/1/Establishment%20of%20contamination-free%2024pgs.pdf text en http://ir.unimas.my/id/eprint/20801/8/Liu%20Yan%20ft.pdf Liu, Yan Tin (2009) Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq. [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)
QR Microbiology
spellingShingle Q Science (General)
QR Microbiology
Liu, Yan Tin
Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq.
description Shorea leprosula Miq., a fast growing dipterocarps, has potential for reforestation of degraded forest. However, planting stock of this species is scarce because fruiting is irregular and the seeds are recalcitrant. Micropropagation has been considered as an alternative to mass produce the planting stock. The objective of this study was to develop an effective surface sterilization protocol to establish contamination-free culture as the first step towards development of micropropagation of S. leprosula. The surface sterilization protocol developed so far started with soaking the fieldderived shoot-tip and nodal explants in a fungicide solution for one and three hours respectively. The explants were then dipped in 75% ethanol for one minute and surface sterilized in 5% Clorox added with Tween 20 for 10 minutes and Chlorine Dioxide at 50 ppm for 10 minutes. The explants were then rinsed with autoclaved-RO water for at least three times. Nodal explants were pulse-treated with 10 ml/L PPM for overnight whereas shoot-tip explants were pulsedtreated with PPM at 5 ml/L for an hour. Surface-sterilized explants were trimmed and cultured on MS basal medium supplemented with 20 g/L sucrose. BAP and TDZ were found to be effective in inducing new buds growth on nodal explants. Nodal explants inoculated on MS basal medium supplemented with 2 mg/L BAP and 0.1 mg/L NAA showed new buds growth.
format Final Year Project Report
author Liu, Yan Tin
author_facet Liu, Yan Tin
author_sort Liu, Yan Tin
title Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq.
title_short Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq.
title_full Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq.
title_fullStr Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq.
title_full_unstemmed Establishment of contamination-free culture and In vitro regeneration of shorea leprosula miq.
title_sort establishment of contamination-free culture and in vitro regeneration of shorea leprosula miq.
publisher unimas
publishDate 2009
url http://ir.unimas.my/id/eprint/20801/1/Establishment%20of%20contamination-free%2024pgs.pdf
http://ir.unimas.my/id/eprint/20801/8/Liu%20Yan%20ft.pdf
http://ir.unimas.my/id/eprint/20801/
_version_ 1802981800608268288
score 13.211869