Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.)

In this research new protocol has been developed that would induce callus from anther and ovary of Kenaf. The haploid technique is a fast and efficient tool for developing new varieties in a comparatively short time. The present study was carried out to investigate the effect of cold treatment, plan...

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Main Authors: Ahmed Mahmood Ibrahim, Fatimah Kayat, Dwi Susanto, Mohammed Ariffulah, Pedram Kashiani
Format: Non-Indexed Article
Published: Universiti Malaysia Kelantan 2015
Online Access:http://discol.umk.edu.my/id/eprint/8024/
http://jtrss.org/JTRSS/volume3/UN-17/3-1-6-13.pdf
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_version_ 1831512472821956608
author Ahmed Mahmood Ibrahim
Fatimah Kayat
Dwi Susanto
Mohammed Ariffulah
Pedram Kashiani
author_facet Ahmed Mahmood Ibrahim
Fatimah Kayat
Dwi Susanto
Mohammed Ariffulah
Pedram Kashiani
author_sort Ahmed Mahmood Ibrahim
building Perpustakaan Universiti Malaysia Kelantan
collection Institutional Repository
content_provider Universiti Malaysia Kelantan
content_source UMK Institutional Repository
continent Asia
country Malaysia
description In this research new protocol has been developed that would induce callus from anther and ovary of Kenaf. The haploid technique is a fast and efficient tool for developing new varieties in a comparatively short time. The present study was carried out to investigate the effect of cold treatment, plant growth regulators (PGR) and culture condition on callus induction from Kenaf anther and ovary culture. Kenaf HF992 cultivar was chosen as an explants material, several trails were carried out to investigate the Androgenesis and gynogenesis ability before we succeed to get high percentage of callus. Flower buds at the appropriate stage of anther and ovary development were sterilized and the anthers and ovary were carefully excised from the flowers and underwent to various pretreatments and inoculated into media contained different combinations of PGR like NAA(anaphthaleneacetic acid), BAP(N6-benzyladenine), 2iP(N6-(2-Isopentenyl) adenine) and TDZ (Thidiazuron)and kept in the dark place for different periods before transferred to light conditions. The best callus induction frequency from anther was 90.00 % in the optimized MS medium fortified with 3.0 mg/l 2iP + 3.0 mg/l NAA at the stage the microspores were at the uninucleate stage and the anther was about 7±1 mm long collected. And the best callus induction frequency from ovary was 91.25% in the optimized semi solid MS medium fortified with 3.0 mg/l 2iP + 3.0 mg/l NAA, and the flower buds was about 24±1 mm length which was collected 3-5 weeks after flower initiation. The effect of culture condition was highly significant, the root induction was highest (83.75% & 87.50%) of anther and ovary respectively when it kept in dark place for 28 days.
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institution Universiti Malaysia Kelantan
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spelling my.umk.eprints.80242022-05-23T10:24:44Z http://discol.umk.edu.my/id/eprint/8024/ Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.) Ahmed Mahmood Ibrahim Fatimah Kayat Dwi Susanto Mohammed Ariffulah Pedram Kashiani In this research new protocol has been developed that would induce callus from anther and ovary of Kenaf. The haploid technique is a fast and efficient tool for developing new varieties in a comparatively short time. The present study was carried out to investigate the effect of cold treatment, plant growth regulators (PGR) and culture condition on callus induction from Kenaf anther and ovary culture. Kenaf HF992 cultivar was chosen as an explants material, several trails were carried out to investigate the Androgenesis and gynogenesis ability before we succeed to get high percentage of callus. Flower buds at the appropriate stage of anther and ovary development were sterilized and the anthers and ovary were carefully excised from the flowers and underwent to various pretreatments and inoculated into media contained different combinations of PGR like NAA(anaphthaleneacetic acid), BAP(N6-benzyladenine), 2iP(N6-(2-Isopentenyl) adenine) and TDZ (Thidiazuron)and kept in the dark place for different periods before transferred to light conditions. The best callus induction frequency from anther was 90.00 % in the optimized MS medium fortified with 3.0 mg/l 2iP + 3.0 mg/l NAA at the stage the microspores were at the uninucleate stage and the anther was about 7±1 mm long collected. And the best callus induction frequency from ovary was 91.25% in the optimized semi solid MS medium fortified with 3.0 mg/l 2iP + 3.0 mg/l NAA, and the flower buds was about 24±1 mm length which was collected 3-5 weeks after flower initiation. The effect of culture condition was highly significant, the root induction was highest (83.75% & 87.50%) of anther and ovary respectively when it kept in dark place for 28 days. Universiti Malaysia Kelantan 2015 Non-Indexed Article NonPeerReviewed Ahmed Mahmood Ibrahim and Fatimah Kayat and Dwi Susanto and Mohammed Ariffulah and Pedram Kashiani (2015) Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.). Journal of Tropical Resources and Sustainable Sciences, 3. pp. 6-13. ISSN 2289-3946 http://jtrss.org/JTRSS/volume3/UN-17/3-1-6-13.pdf
spellingShingle Ahmed Mahmood Ibrahim
Fatimah Kayat
Dwi Susanto
Mohammed Ariffulah
Pedram Kashiani
Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.)
title Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.)
title_full Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.)
title_fullStr Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.)
title_full_unstemmed Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.)
title_short Callus induction through Anther and Ovary of Kenaf (Hibiscus cannabinus L.)
title_sort callus induction through anther and ovary of kenaf (hibiscus cannabinus l.)
url http://discol.umk.edu.my/id/eprint/8024/
http://jtrss.org/JTRSS/volume3/UN-17/3-1-6-13.pdf
url_provider http://discol.umk.edu.my/