Horizon / Plein textes La base de ressources documentaires de l'IRD

IRD

Publications des scientifiques de l'IRD

Rey H. Y., Faloci M., Medina R., Dolce N., Mroyinski L., Engelmann Florent. Cryopreservation of in vitro grown shoot tips and apical meristems of the forage legume Arachis pintoi. Cryoletters, 2009, 30 (5), p. 347-358. ISSN 0143-2044

Accès réservé (Intranet IRD) Document en accès réservé (Intranet IRD)

Titre
Cryopreservation of in vitro grown shoot tips and apical meristems of the forage legume Arachis pintoi
Année de publication2009
Type de documentArticle référencé dans le Web of Science WOS:000272548000004
AuteursRey H. Y., Faloci M., Medina R., Dolce N., Mroyinski L., Engelmann Florent.
SourceCryoletters, 2009, 30 (5), p. 347-358. ISSN 0143-2044
RésuméA cryopreservation protocol using the encapsulation-dehydration procedure was established for shoot tips (2-3 mm in length) and meristems (0.3-0.5 mm) sampled from in vitro plantlets of diploid and triploid cytotypes of Arachis pintoi. The optimal protocol was the following: after dissection, explants were precultured for 24 h on establishment medium (EM), encapsulated in calcium alginate beads and pretreated in liquid EM medium with daily increasing sucrose concentration (0.5, 0.75, 1.0 M) and desiccated to 22-23% moisture content (fresh weight basis). Explants were frozen using slow cooling (1 degrees C min(-1) from 25 degrees C to -30 degrees C followed by direct immersion in liquid nitrogen), thawed rapidly and post-cultured in liquid EM medium enriched with daily decreasing sucrose concentrations (0.75, 0.50, 0.1 M). Explants were then transferred to solid EM medium in order to achieve shoot regeneration, then on Murashige and Skoog medium supplemented with 0.05 mu M naphthalene acetic acid to induce rooting of shoots. With this procedure, 53% and 56% of cryopreserved shoot tips of the diploid and triploid cytotypes, respectively, survived and formed plants. However, only 16% of cryopreserved meristems of both cytotypes regenerated plants. Using ten isozyme systems and seven RAPD profiles, no modification induced by cryopreservation could be detected in plantlets regenerated from cryopreserved material.
Plan de classement076
LocalisationFonds IRD [F B010048479] ; Montpellier (Centre IRD)
Identifiant IRDfdi:010048479
Lien permanenthttp://www.documentation.ird.fr/hor/fdi:010048479

Export des données

Accès direct

Bureau du chercheur

Site de la documentation

Espace intranet IST (accès réservé)

Suivi des publications IRD (accès réservé)

Mentions légales

Services Horizon

Poser une question

Consulter l'aide en ligne

Déposer une publication (accès réservé)

S'abonner au flux RSS

Voir les tableaux chronologiques et thématiques

Centres de documentation

Bondy

Montpellier (centre IRD)

Montpellier (MSE)

Cayenne

Nouméa

Papeete

Abidjan

Dakar

Niamey

Ouagadougou

Tunis

La Paz

Quito