Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor

Germination and subsequent development was assessed after seeds of Vanda tricolor were stored in liquid nitrogen. Mature seeds, harvested 7 months after self-pollination, were directly plunged into liquid nitrogen. Germination of cryopreserved seeds on solid New Dogashima (ND) medium supplemented wi...

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Main Authors: Nipawan Jitsopakul, Kanchit Thammasiri, Tomohisa Yukawa, Keiko Ishikawa
Other Authors: Rajamangala University of Technology Isan
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/15242
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spelling th-mahidol.152422018-06-11T12:27:38Z Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor Nipawan Jitsopakul Kanchit Thammasiri Tomohisa Yukawa Keiko Ishikawa Rajamangala University of Technology Isan Mahidol University National Science Museum, Tokyo Japan Horticultural Production and Research Institute Multidisciplinary Germination and subsequent development was assessed after seeds of Vanda tricolor were stored in liquid nitrogen. Mature seeds, harvested 7 months after self-pollination, were directly plunged into liquid nitrogen. Germination of cryopreserved seeds on solid New Dogashima (ND) medium supplemented with 1 mg/l 6-benzyladenine, 0.5 mg/l 1-naphthaleneacetic acid and 2% sucrose was faster than non-cryopreserved seeds (28 days versus 60 days after sowing). Immature seeds, harvested 6 months after self-pollination, were treated with or without loading solution (LS) of 2Mglycerol and 0.4 M sucrose in liquid ND medium, pH 5.4 at 25°C for 15 min and dehydrated with PVS2 solution for 0-210 min on ice and then cryopreserved by vitrification. The results showed that the germination percentage of cryopreserved seeds treated with LS was higher than without LS. After 90 days of sowing, the highest germination percentage of cryopreserved seeds was 13.6% which was higher than non-cryopreserved seeds (10.5%) when seeds were treated with LS for 15 min and then dehydrated with PVS2 solution for 180 min. After 150 days of sowing, protocorms of non-cryopreserved and cryopreserved seeds were able to form new protocorms (budding protocorms) and developed into shoots after 180 days of sowing. There were no significant differences between growth and development of protocorms derived from noncryopreserved and cryopreserved seeds. Copyright © 2005 ScienceAsia. 2018-06-11T05:27:38Z 2018-06-11T05:27:38Z 2012-09-01 Article ScienceAsia. Vol.38, No.3 (2012), 244-249 10.2306/scienceasia1513-1874.2012.38.244 15131874 2-s2.0-84870821903 https://repository.li.mahidol.ac.th/handle/123456789/15242 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870821903&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Multidisciplinary
spellingShingle Multidisciplinary
Nipawan Jitsopakul
Kanchit Thammasiri
Tomohisa Yukawa
Keiko Ishikawa
Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor
description Germination and subsequent development was assessed after seeds of Vanda tricolor were stored in liquid nitrogen. Mature seeds, harvested 7 months after self-pollination, were directly plunged into liquid nitrogen. Germination of cryopreserved seeds on solid New Dogashima (ND) medium supplemented with 1 mg/l 6-benzyladenine, 0.5 mg/l 1-naphthaleneacetic acid and 2% sucrose was faster than non-cryopreserved seeds (28 days versus 60 days after sowing). Immature seeds, harvested 6 months after self-pollination, were treated with or without loading solution (LS) of 2Mglycerol and 0.4 M sucrose in liquid ND medium, pH 5.4 at 25°C for 15 min and dehydrated with PVS2 solution for 0-210 min on ice and then cryopreserved by vitrification. The results showed that the germination percentage of cryopreserved seeds treated with LS was higher than without LS. After 90 days of sowing, the highest germination percentage of cryopreserved seeds was 13.6% which was higher than non-cryopreserved seeds (10.5%) when seeds were treated with LS for 15 min and then dehydrated with PVS2 solution for 180 min. After 150 days of sowing, protocorms of non-cryopreserved and cryopreserved seeds were able to form new protocorms (budding protocorms) and developed into shoots after 180 days of sowing. There were no significant differences between growth and development of protocorms derived from noncryopreserved and cryopreserved seeds. Copyright © 2005 ScienceAsia.
author2 Rajamangala University of Technology Isan
author_facet Rajamangala University of Technology Isan
Nipawan Jitsopakul
Kanchit Thammasiri
Tomohisa Yukawa
Keiko Ishikawa
format Article
author Nipawan Jitsopakul
Kanchit Thammasiri
Tomohisa Yukawa
Keiko Ishikawa
author_sort Nipawan Jitsopakul
title Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor
title_short Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor
title_full Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor
title_fullStr Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor
title_full_unstemmed Effect of cryopreservation on seed germination and protocorm development of Vanda tricolor
title_sort effect of cryopreservation on seed germination and protocorm development of vanda tricolor
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/15242
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