In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germination

The objective of this study is to establish an in vitro germination and cultivation protocol for murici (Byrsonima cydoniifolia A. Juss.) using zygotic embryos. Therefore, three assays were performed: in assay I, embryo asepsis was tested at exposure times of 5, 10, 15, 20, 25, and 30 minutes in 2.5% sodium hypochlorite, with or without immersion in 70% alcohol; in assay II, MS (MURASHIGE; SKOOG, 1962) e WPM (LLOYD; McCOWN, 1980) culture media were tested at salt concentrations of 25, 50, and 100%, with or without the addition of sucrose, to germinate the buds; in assay III, seedling growth was evaluated in MS and WPM culture media at salt concentrations of 25, 50 and 100%. Sodium hypochlorite (2.5%) with or without 70% alcohol was used to avoid contamination because it was not toxic to murici embryos. Water-agar was the most appropriate culture medium for bud germination, and 50% WPM was appropriate for seedling growth.

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Main Authors: Martendal,Cíntia de Oliveira, Bernardino,Murilo Martins, Pereira,Flávia Dionísio, Silva,Fabiano Guimarães, Menezes,Carlos César Evangelista de, Hara,Alessandra Cristina Boffino de Almeida Monteiro
Format: Digital revista
Language:English
Published: Editora da Universidade Estadual de Maringá - EDUEM 2013
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1807-86212013000200011
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spelling oai:scielo:S1807-862120130002000112013-04-16In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germinationMartendal,Cíntia de OliveiraBernardino,Murilo MartinsPereira,Flávia DionísioSilva,Fabiano GuimarãesMenezes,Carlos César Evangelista deHara,Alessandra Cristina Boffino de Almeida Monteiro tissue culture asepsis culture medium Cerrado fruit The objective of this study is to establish an in vitro germination and cultivation protocol for murici (Byrsonima cydoniifolia A. Juss.) using zygotic embryos. Therefore, three assays were performed: in assay I, embryo asepsis was tested at exposure times of 5, 10, 15, 20, 25, and 30 minutes in 2.5% sodium hypochlorite, with or without immersion in 70% alcohol; in assay II, MS (MURASHIGE; SKOOG, 1962) e WPM (LLOYD; McCOWN, 1980) culture media were tested at salt concentrations of 25, 50, and 100%, with or without the addition of sucrose, to germinate the buds; in assay III, seedling growth was evaluated in MS and WPM culture media at salt concentrations of 25, 50 and 100%. Sodium hypochlorite (2.5%) with or without 70% alcohol was used to avoid contamination because it was not toxic to murici embryos. Water-agar was the most appropriate culture medium for bud germination, and 50% WPM was appropriate for seedling growth.info:eu-repo/semantics/openAccessEditora da Universidade Estadual de Maringá - EDUEMActa Scientiarum. Agronomy v.35 n.2 20132013-06-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1807-86212013000200011en10.4025/actasciagron.v35i2.15402
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Martendal,Cíntia de Oliveira
Bernardino,Murilo Martins
Pereira,Flávia Dionísio
Silva,Fabiano Guimarães
Menezes,Carlos César Evangelista de
Hara,Alessandra Cristina Boffino de Almeida Monteiro
spellingShingle Martendal,Cíntia de Oliveira
Bernardino,Murilo Martins
Pereira,Flávia Dionísio
Silva,Fabiano Guimarães
Menezes,Carlos César Evangelista de
Hara,Alessandra Cristina Boffino de Almeida Monteiro
In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germination
author_facet Martendal,Cíntia de Oliveira
Bernardino,Murilo Martins
Pereira,Flávia Dionísio
Silva,Fabiano Guimarães
Menezes,Carlos César Evangelista de
Hara,Alessandra Cristina Boffino de Almeida Monteiro
author_sort Martendal,Cíntia de Oliveira
title In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germination
title_short In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germination
title_full In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germination
title_fullStr In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germination
title_full_unstemmed In vitro cultivation of zygotic embryos from Murici (Byrsonima cydoniifolia A. Juss. ): establishment, disinfection, and germination
title_sort in vitro cultivation of zygotic embryos from murici (byrsonima cydoniifolia a. juss. ): establishment, disinfection, and germination
description The objective of this study is to establish an in vitro germination and cultivation protocol for murici (Byrsonima cydoniifolia A. Juss.) using zygotic embryos. Therefore, three assays were performed: in assay I, embryo asepsis was tested at exposure times of 5, 10, 15, 20, 25, and 30 minutes in 2.5% sodium hypochlorite, with or without immersion in 70% alcohol; in assay II, MS (MURASHIGE; SKOOG, 1962) e WPM (LLOYD; McCOWN, 1980) culture media were tested at salt concentrations of 25, 50, and 100%, with or without the addition of sucrose, to germinate the buds; in assay III, seedling growth was evaluated in MS and WPM culture media at salt concentrations of 25, 50 and 100%. Sodium hypochlorite (2.5%) with or without 70% alcohol was used to avoid contamination because it was not toxic to murici embryos. Water-agar was the most appropriate culture medium for bud germination, and 50% WPM was appropriate for seedling growth.
publisher Editora da Universidade Estadual de Maringá - EDUEM
publishDate 2013
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1807-86212013000200011
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