Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.

This work reports on the cryopreservation of immature zygotic embryonic axes (EA) of petai (Parkia speciosa Hassk.) for the first time. Two cryopreservation protocols, namely desiccation and vitrification method were tested individually using excised EA. Desiccation of EA to lower moisture content (...

Full description

Saved in:
Bibliographic Details
Main Authors: Sinniah, Uma Rani, Gantait, Saikat
Format: Article
Language:English
English
Published: Springer Berlin Heidelberg 2013
Online Access:http://psasir.upm.edu.my/id/eprint/29492/1/Cryopreservation%20of%20immature%20Parkia%20speciosa%20Hassk.pdf
http://psasir.upm.edu.my/id/eprint/29492/
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Universiti Putra Malaysia
Language: English
English
id my.upm.eprints.29492
record_format eprints
spelling my.upm.eprints.294922016-02-03T02:55:38Z http://psasir.upm.edu.my/id/eprint/29492/ Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution. Sinniah, Uma Rani Gantait, Saikat This work reports on the cryopreservation of immature zygotic embryonic axes (EA) of petai (Parkia speciosa Hassk.) for the first time. Two cryopreservation protocols, namely desiccation and vitrification method were tested individually using excised EA. Desiccation of EA to lower moisture content (MC) reduced the survival percentage but a drastic decline in survival percentage (~20 %) was recorded at 16 % MC prior to exposure to LN, rendering the EA to be sensitive to desiccation. Cryopreservation of EA after desiccation, irrespective of the MC, did not result in any survival. On the other hand, post-cryopreservation survival was obtained when the EA were exposed to plant vitrification solution-2 (PVS2) for 75–105 min. The best results were obtained when the EA were exposed to PVS2 for 90 min with an average recovery of 55.5 %. EA recovery into whole plantlets was obtained when the EA were cultured on MS medium supplemented with 2 gl−1 activated charcoal and 0.1 mgl−1 of the plant growth regulators α-naphthalene acetic acid, 6-benzylaminopurine and gibberellin A3, each. EA, exposed for less than 75 min and more than 105 min to PVS2, did not show any survival after cryopreservation. The optimization of exposure time is necessary to increase survival. This study has shown that the employment of suitable method is important for conservation using cryopreservation. Springer Berlin Heidelberg 2013 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/29492/1/Cryopreservation%20of%20immature%20Parkia%20speciosa%20Hassk.pdf Sinniah, Uma Rani and Gantait, Saikat (2013) Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution. Acta Physiologiae Plantarum, 35 (8). pp. 2629-2634. ISSN 0137-5881; ESSN: 1861-1664 10.1007/s11738-013-1284-z English
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
English
description This work reports on the cryopreservation of immature zygotic embryonic axes (EA) of petai (Parkia speciosa Hassk.) for the first time. Two cryopreservation protocols, namely desiccation and vitrification method were tested individually using excised EA. Desiccation of EA to lower moisture content (MC) reduced the survival percentage but a drastic decline in survival percentage (~20 %) was recorded at 16 % MC prior to exposure to LN, rendering the EA to be sensitive to desiccation. Cryopreservation of EA after desiccation, irrespective of the MC, did not result in any survival. On the other hand, post-cryopreservation survival was obtained when the EA were exposed to plant vitrification solution-2 (PVS2) for 75–105 min. The best results were obtained when the EA were exposed to PVS2 for 90 min with an average recovery of 55.5 %. EA recovery into whole plantlets was obtained when the EA were cultured on MS medium supplemented with 2 gl−1 activated charcoal and 0.1 mgl−1 of the plant growth regulators α-naphthalene acetic acid, 6-benzylaminopurine and gibberellin A3, each. EA, exposed for less than 75 min and more than 105 min to PVS2, did not show any survival after cryopreservation. The optimization of exposure time is necessary to increase survival. This study has shown that the employment of suitable method is important for conservation using cryopreservation.
format Article
author Sinniah, Uma Rani
Gantait, Saikat
spellingShingle Sinniah, Uma Rani
Gantait, Saikat
Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.
author_facet Sinniah, Uma Rani
Gantait, Saikat
author_sort Sinniah, Uma Rani
title Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.
title_short Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.
title_full Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.
title_fullStr Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.
title_full_unstemmed Cryopreservation of immature Parkia speciosa Hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.
title_sort cryopreservation of immature parkia speciosa hassk. zygotic embryonic axes following desiccation or exposure to vitrification solution.
publisher Springer Berlin Heidelberg
publishDate 2013
url http://psasir.upm.edu.my/id/eprint/29492/1/Cryopreservation%20of%20immature%20Parkia%20speciosa%20Hassk.pdf
http://psasir.upm.edu.my/id/eprint/29492/
_version_ 1643829775909781504