Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production

Somatic embryogenesis in cork oak (Quercus suber L.) is an efficient tool that allows the production of large number of embryos from selected quality and productive trees. Temporary immersion systems (TIS) are an alternative to semi-solid or liquid culture that combine the advantages of liquid culture and avoid the associated problems. Parameters that affect the TIS multiplication efficiency of Q. suber L. embryogenic cultures were evaluated. Immersion frequencies of 1 min every 6 or 4 h increased the fresh weight 3.7 or 7.5-fold compared with an immersion frequency of 1 min every 12 h or cultures on semi-solid medium, respectively. The cellular fate of embryogenic cultures was also affected by the immersion frequency, 1 min every 6 h was the best for mass propagation of proliferative developmental stages (embryogenic calli and embryo clusters) while 1 min every 4 h promoted the formation of single, fully developed cotyledonary embryos. An initial amount of 1.5 g fresh weight of proliferative tissues produced the best results in RITA® containers while 0.5 g of embryogenic callus was the best for semi-solid cultures. © 2013 Springer-Verlag Berlin Heidelberg.

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Main Authors: Pérez, M., Bueno, M. A., Escalona, M., Toorop, P., Rodríguez, R., Cañal, M. J.
Format: journal article biblioteca
Language:eng
Published: 2013
Online Access:http://hdl.handle.net/20.500.12792/3400
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spelling dig-inia-es-20.500.12792-34002020-12-15T09:54:30Z Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production Pérez, M. Bueno, M. A. Escalona, M. Toorop, P. Rodríguez, R. Cañal, M. J. Somatic embryogenesis in cork oak (Quercus suber L.) is an efficient tool that allows the production of large number of embryos from selected quality and productive trees. Temporary immersion systems (TIS) are an alternative to semi-solid or liquid culture that combine the advantages of liquid culture and avoid the associated problems. Parameters that affect the TIS multiplication efficiency of Q. suber L. embryogenic cultures were evaluated. Immersion frequencies of 1 min every 6 or 4 h increased the fresh weight 3.7 or 7.5-fold compared with an immersion frequency of 1 min every 12 h or cultures on semi-solid medium, respectively. The cellular fate of embryogenic cultures was also affected by the immersion frequency, 1 min every 6 h was the best for mass propagation of proliferative developmental stages (embryogenic calli and embryo clusters) while 1 min every 4 h promoted the formation of single, fully developed cotyledonary embryos. An initial amount of 1.5 g fresh weight of proliferative tissues produced the best results in RITA® containers while 0.5 g of embryogenic callus was the best for semi-solid cultures. © 2013 Springer-Verlag Berlin Heidelberg. 2020-10-22T14:36:32Z 2020-10-22T14:36:32Z 2013 journal article http://hdl.handle.net/20.500.12792/3400 10.1007/s00468-013-0876-y eng Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ open access
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country España
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region Europa del Sur
libraryname Biblioteca del INIA España
language eng
description Somatic embryogenesis in cork oak (Quercus suber L.) is an efficient tool that allows the production of large number of embryos from selected quality and productive trees. Temporary immersion systems (TIS) are an alternative to semi-solid or liquid culture that combine the advantages of liquid culture and avoid the associated problems. Parameters that affect the TIS multiplication efficiency of Q. suber L. embryogenic cultures were evaluated. Immersion frequencies of 1 min every 6 or 4 h increased the fresh weight 3.7 or 7.5-fold compared with an immersion frequency of 1 min every 12 h or cultures on semi-solid medium, respectively. The cellular fate of embryogenic cultures was also affected by the immersion frequency, 1 min every 6 h was the best for mass propagation of proliferative developmental stages (embryogenic calli and embryo clusters) while 1 min every 4 h promoted the formation of single, fully developed cotyledonary embryos. An initial amount of 1.5 g fresh weight of proliferative tissues produced the best results in RITA® containers while 0.5 g of embryogenic callus was the best for semi-solid cultures. © 2013 Springer-Verlag Berlin Heidelberg.
format journal article
author Pérez, M.
Bueno, M. A.
Escalona, M.
Toorop, P.
Rodríguez, R.
Cañal, M. J.
spellingShingle Pérez, M.
Bueno, M. A.
Escalona, M.
Toorop, P.
Rodríguez, R.
Cañal, M. J.
Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production
author_facet Pérez, M.
Bueno, M. A.
Escalona, M.
Toorop, P.
Rodríguez, R.
Cañal, M. J.
author_sort Pérez, M.
title Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production
title_short Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production
title_full Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production
title_fullStr Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production
title_full_unstemmed Temporary immersion systems (RITA®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production
title_sort temporary immersion systems (rita®) for the improvement of cork oak somatic embryogenic culture proliferation and somatic embryo production
publishDate 2013
url http://hdl.handle.net/20.500.12792/3400
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