Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)

Detalhes bibliográficos
Autor(a) principal: Canhoto, Jorge
Data de Publicação: 2006
Outros Autores: Rama, Sandra, Cruz, Gil
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/7576
https://doi.org/10.1079/IVP2006819
Resumo: Summary Somatic embryos of carob (Ceratonia siliqua L.) were induced from cotyledonary segments excised from immature seeds when cultured on Murashige and Skoog media supplemented with several combinations of 6-benzylaminopurine (BA) and indole-3-butyric acid (IBA). The best frequencies of induction (33.8%) were obtained when 4.4 µM BA and 0.5 µM IBA were used. Shoots were also sporadically formed in the same media. When IBA was replaced by other auxins in the induction media, only a-naphthaleneacetic acid (NAA) and indole-3-acetic acid (IAA) could induce somatic embryogenesis, although at lower rates than IBA. 2,4-Dichlorophenoxyacetic acid and 4-amino-3,5,6-trichloropicolinic acid were completely ineffective. Besides culture media composition, the developmental stage of the explants at the time of culture showed a strong influence on somatic embryogenesis induction, with cotyledons from stage II pods providing the highest levels of induction. By contrast, the genotype of the explant did not determine a significant role in the induction process. Attempts to achieve somatic embryo germination were mostly unsuccessful, since only shoot development was observed; the highest frequencies of development occurred on media containing only gibberellic acid (3.0 µM). For plant regeneration, the developed shoots were further rooted on IBA-supplemented media, and the plantlets obtained were transferred to soil, where c. 88% of them survived. Histological observations showed the presence of morphologically normal and abnormal somatic embryos, the latter displaying an abnormal pattern of vascular bundles. Ultrastructural analysis showed that the cells of the globular embryos had a dense cytoplasm, whereas those not involved in somatic embryo formation showed signs of senescence. Histological studies were also used to distinguish between somatic embryos and shoots originated in the same media.
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spelling Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)Summary Somatic embryos of carob (Ceratonia siliqua L.) were induced from cotyledonary segments excised from immature seeds when cultured on Murashige and Skoog media supplemented with several combinations of 6-benzylaminopurine (BA) and indole-3-butyric acid (IBA). The best frequencies of induction (33.8%) were obtained when 4.4 µM BA and 0.5 µM IBA were used. Shoots were also sporadically formed in the same media. When IBA was replaced by other auxins in the induction media, only a-naphthaleneacetic acid (NAA) and indole-3-acetic acid (IAA) could induce somatic embryogenesis, although at lower rates than IBA. 2,4-Dichlorophenoxyacetic acid and 4-amino-3,5,6-trichloropicolinic acid were completely ineffective. Besides culture media composition, the developmental stage of the explants at the time of culture showed a strong influence on somatic embryogenesis induction, with cotyledons from stage II pods providing the highest levels of induction. By contrast, the genotype of the explant did not determine a significant role in the induction process. Attempts to achieve somatic embryo germination were mostly unsuccessful, since only shoot development was observed; the highest frequencies of development occurred on media containing only gibberellic acid (3.0 µM). For plant regeneration, the developed shoots were further rooted on IBA-supplemented media, and the plantlets obtained were transferred to soil, where c. 88% of them survived. Histological observations showed the presence of morphologically normal and abnormal somatic embryos, the latter displaying an abnormal pattern of vascular bundles. Ultrastructural analysis showed that the cells of the globular embryos had a dense cytoplasm, whereas those not involved in somatic embryo formation showed signs of senescence. Histological studies were also used to distinguish between somatic embryos and shoots originated in the same media.2006info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/7576http://hdl.handle.net/10316/7576https://doi.org/10.1079/IVP2006819engIn Vitro Cellular & Developmental Biology - Plant. 42:6 (2006) 514-519Canhoto, JorgeRama, SandraCruz, Gilinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-05-29T09:41:59Zoai:estudogeral.uc.pt:10316/7576Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:55:45.558577Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
title Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
spellingShingle Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
Canhoto, Jorge
title_short Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
title_full Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
title_fullStr Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
title_full_unstemmed Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
title_sort Somatic embryogenesis and plant regeneration in carob ( Ceratonia siliqua L.)
author Canhoto, Jorge
author_facet Canhoto, Jorge
Rama, Sandra
Cruz, Gil
author_role author
author2 Rama, Sandra
Cruz, Gil
author2_role author
author
dc.contributor.author.fl_str_mv Canhoto, Jorge
Rama, Sandra
Cruz, Gil
description Summary Somatic embryos of carob (Ceratonia siliqua L.) were induced from cotyledonary segments excised from immature seeds when cultured on Murashige and Skoog media supplemented with several combinations of 6-benzylaminopurine (BA) and indole-3-butyric acid (IBA). The best frequencies of induction (33.8%) were obtained when 4.4 µM BA and 0.5 µM IBA were used. Shoots were also sporadically formed in the same media. When IBA was replaced by other auxins in the induction media, only a-naphthaleneacetic acid (NAA) and indole-3-acetic acid (IAA) could induce somatic embryogenesis, although at lower rates than IBA. 2,4-Dichlorophenoxyacetic acid and 4-amino-3,5,6-trichloropicolinic acid were completely ineffective. Besides culture media composition, the developmental stage of the explants at the time of culture showed a strong influence on somatic embryogenesis induction, with cotyledons from stage II pods providing the highest levels of induction. By contrast, the genotype of the explant did not determine a significant role in the induction process. Attempts to achieve somatic embryo germination were mostly unsuccessful, since only shoot development was observed; the highest frequencies of development occurred on media containing only gibberellic acid (3.0 µM). For plant regeneration, the developed shoots were further rooted on IBA-supplemented media, and the plantlets obtained were transferred to soil, where c. 88% of them survived. Histological observations showed the presence of morphologically normal and abnormal somatic embryos, the latter displaying an abnormal pattern of vascular bundles. Ultrastructural analysis showed that the cells of the globular embryos had a dense cytoplasm, whereas those not involved in somatic embryo formation showed signs of senescence. Histological studies were also used to distinguish between somatic embryos and shoots originated in the same media.
publishDate 2006
dc.date.none.fl_str_mv 2006
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/7576
http://hdl.handle.net/10316/7576
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url http://hdl.handle.net/10316/7576
https://doi.org/10.1079/IVP2006819
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dc.relation.none.fl_str_mv In Vitro Cellular & Developmental Biology - Plant. 42:6 (2006) 514-519
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