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Cryopreservation of non-encapsulated embryogenic tissue of sweet potato (Ipomoea batatas)
Embryogenic tissue of the sweet potato (Ipomoea batatas (L) LAM) genotype TIB 10 was established from in vitro axillary shoot tips on Murashige and Skoog (1962) medium supplemented with 5 μM 2,4-dichlorophenoxyacetic acid. Embryogenic aggregates of fresh mass 9.0-12 mg were subjected to a rapid free...
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Published in: | Plant cell reports 1996-08, Vol.15 (11), p.873-876 |
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creator | BLAKESLEY, D AL MAZROOEI, S BHATTI, M. H HENSHAW, G. G |
description | Embryogenic tissue of the sweet potato (Ipomoea batatas (L) LAM) genotype TIB 10 was established from in vitro axillary shoot tips on Murashige and Skoog (1962) medium supplemented with 5 μM 2,4-dichlorophenoxyacetic acid. Embryogenic aggregates of fresh mass 9.0-12 mg were subjected to a rapid freezing protocol in liquid nitrogen following sucrose preculture and varying degrees of dehydration. Up to 50% of embryogenic explants survived rapid freezing after preculture on 0.4 or 0.7M sucrose only. Dehydration with silica gel to moisture contents in the range 18-41% improved the survival after cryopreservation of embryogenic tissue. Tissue dehydrated for intermediate periods exhibited poor survival. Following freezing, embryogenic tissue appeared to develop normally, retaining its competence to produce mature embryos and plantlets. |
doi_str_mv | 10.1007/bf00233160 |
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Following freezing, embryogenic tissue appeared to develop normally, retaining its competence to produce mature embryos and plantlets.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Establishment of new cell lines, improvement of cultural methods, mass culture</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ipomoea batatas</subject><subject>Methods. Procedures. 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Psychology</topic><topic>Ipomoea batatas</topic><topic>Methods. Procedures. Technologies</topic><topic>Plant cells and fungal cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BLAKESLEY, D</creatorcontrib><creatorcontrib>AL MAZROOEI, S</creatorcontrib><creatorcontrib>BHATTI, M. H</creatorcontrib><creatorcontrib>HENSHAW, G. G</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Plant cell reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BLAKESLEY, D</au><au>AL MAZROOEI, S</au><au>BHATTI, M. 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Dehydration with silica gel to moisture contents in the range 18-41% improved the survival after cryopreservation of embryogenic tissue. Tissue dehydrated for intermediate periods exhibited poor survival. Following freezing, embryogenic tissue appeared to develop normally, retaining its competence to produce mature embryos and plantlets.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>24178228</pmid><doi>10.1007/bf00233160</doi><tpages>4</tpages></addata></record> |
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subjects | Biological and medical sciences Biotechnology Establishment of new cell lines, improvement of cultural methods, mass culture Eukaryotic cell cultures Fundamental and applied biological sciences. Psychology Ipomoea batatas Methods. Procedures. Technologies Plant cells and fungal cells |
title | Cryopreservation of non-encapsulated embryogenic tissue of sweet potato (Ipomoea batatas) |
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