High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata)

In vitro culture has been recognized as a potential plant clonal propagation tool for a broad variety of commercial, ornamental, and medicinal species, with applications in both industrial and academic laboratories. In this study, we describe somatic embryogenesis and plant regeneration protocol for...

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Main Authors: Goytia Bertero, Valentina, Beznec, Ailin, Faccio, Paula Daniela, Auteri, Micol Tais, Arteaga, Martin, Bonafede, Marcos, Bossio, Maria Emilia
Format: Artículo
Language:Inglés
Published: Springer 2020
Subjects:
Online Access:http://hdl.handle.net/20.500.12123/8145
https://link.springer.com/article/10.1007%2Fs11627-020-10098-5
https://doi.org/10.1007/s11627-020-10098-5
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author Goytia Bertero, Valentina
Beznec, Ailin
Faccio, Paula Daniela
Auteri, Micol Tais
Arteaga, Martin
Bonafede, Marcos
Bossio, Maria Emilia
author_browse Arteaga, Martin
Auteri, Micol Tais
Beznec, Ailin
Bonafede, Marcos
Bossio, Maria Emilia
Faccio, Paula Daniela
Goytia Bertero, Valentina
author_facet Goytia Bertero, Valentina
Beznec, Ailin
Faccio, Paula Daniela
Auteri, Micol Tais
Arteaga, Martin
Bonafede, Marcos
Bossio, Maria Emilia
author_sort Goytia Bertero, Valentina
collection INTA Digital
description In vitro culture has been recognized as a potential plant clonal propagation tool for a broad variety of commercial, ornamental, and medicinal species, with applications in both industrial and academic laboratories. In this study, we describe somatic embryogenesis and plant regeneration protocol for “peperina” plants (Minthostachys verticillata (Griseb.) Epling). In vitro shoots developed via shoot apex extracted from greenhouse-grown plants were cultured on shoot elongation medium (ShM) consisting of Murashige and Skoog (MS) basal salts supplemented with myoinositol, thiamine, and benzyladenine. Shoot apexes were disinfected with 70% ethanol for 5 min and 0.26 sodium hypochlorite (w/v) for 5 min, before the initiation of in vitro culture. For somatic embryo (SE) induction, leaves collected from 2-mo-old in vitro raised shoots were cultured on MS basal medium supplemented with benzyladenine and two different concentrations of coconut water (CW) until SE developed. Using 2.5% CW-supplemented medium, 100% of cultured leaves developed SE and 89.3% of the leaf explants developed plantlets. The resulting embryos germinated on the same medium, and the plantlets obtained were transferred onto ShM until they developed 3 to 4 leaves. To increase the low root development, shoots were transferred into fully hydrated perlite for rooting and then transplanted into soil-perlite containing pots for hardening. This protocol provides the first step to supply the demand and simultaneously protect the natural populations of Minthostachys verticillata from overexploitation. Furthermore, this protocol provides the first step for crop improvement by genetic modification (editing or transgenesis).
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spelling INTA81452020-10-28T22:35:09Z High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata) Goytia Bertero, Valentina Beznec, Ailin Faccio, Paula Daniela Auteri, Micol Tais Arteaga, Martin Bonafede, Marcos Bossio, Maria Emilia Minthostachys Somatic Embryogenesis In Vitro Culture Embriogénesis Somática Cultivo in Vitro Griseb Peperina In vitro culture has been recognized as a potential plant clonal propagation tool for a broad variety of commercial, ornamental, and medicinal species, with applications in both industrial and academic laboratories. In this study, we describe somatic embryogenesis and plant regeneration protocol for “peperina” plants (Minthostachys verticillata (Griseb.) Epling). In vitro shoots developed via shoot apex extracted from greenhouse-grown plants were cultured on shoot elongation medium (ShM) consisting of Murashige and Skoog (MS) basal salts supplemented with myoinositol, thiamine, and benzyladenine. Shoot apexes were disinfected with 70% ethanol for 5 min and 0.26 sodium hypochlorite (w/v) for 5 min, before the initiation of in vitro culture. For somatic embryo (SE) induction, leaves collected from 2-mo-old in vitro raised shoots were cultured on MS basal medium supplemented with benzyladenine and two different concentrations of coconut water (CW) until SE developed. Using 2.5% CW-supplemented medium, 100% of cultured leaves developed SE and 89.3% of the leaf explants developed plantlets. The resulting embryos germinated on the same medium, and the plantlets obtained were transferred onto ShM until they developed 3 to 4 leaves. To increase the low root development, shoots were transferred into fully hydrated perlite for rooting and then transplanted into soil-perlite containing pots for hardening. This protocol provides the first step to supply the demand and simultaneously protect the natural populations of Minthostachys verticillata from overexploitation. Furthermore, this protocol provides the first step for crop improvement by genetic modification (editing or transgenesis). Fil: Goytia Bertero, Valentina. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Genética; Argentina. Universidad de Morón. Facultad de Ciencias Exactas Químicas y Naturales. Cátedra de Ingeniería Genética; Argentina Fil: Beznec, Ailin. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Genética; Argentina. Universidad de Morón. Facultad de Ciencias Exactas, Químicas y Naturales; Argentina Fil: Faccio, Paula Daniela. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Genética; Argentina. Universidad de Morón. Facultad de Ciencias Exactas, Químicas y Naturales; Argentina Fil: Arteaga, Martín. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Recursos Biológicos; Argentina Fil: Bonafede, Marcos. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Recursos Biológicos; Argentina Fil: Bossio, Adrian Ezequiel. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Genética; Argentina. Universidad de Morón. Facultad de Ciencias Exactas, Químicas y Naturales; Argentina Fil: Auteri, Micol Tais. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Genética; Argentina. Universidad de Morón. Facultad de Ciencias Exactas, Químicas y Naturales. Cátedra de Ingeniería Genética; Argentina 2020-10-28T22:16:35Z 2020-10-28T22:16:35Z 2020-07-30 info:ar-repo/semantics/artículo info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://hdl.handle.net/20.500.12123/8145 https://link.springer.com/article/10.1007%2Fs11627-020-10098-5 1054-5476 https://doi.org/10.1007/s11627-020-10098-5 eng info:eu-repo/semantics/restrictedAccess application/pdf Springer In Vitro Cellular & Developmental Biology - Plant (2020)
spellingShingle Minthostachys
Somatic Embryogenesis
In Vitro Culture
Embriogénesis Somática
Cultivo in Vitro
Griseb
Peperina
Goytia Bertero, Valentina
Beznec, Ailin
Faccio, Paula Daniela
Auteri, Micol Tais
Arteaga, Martin
Bonafede, Marcos
Bossio, Maria Emilia
High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata)
title High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata)
title_full High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata)
title_fullStr High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata)
title_full_unstemmed High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata)
title_short High - efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of "peperina" (Minthostachys verticillata)
title_sort high efficiency direst somatic embryogenesis and plant regeneration from leaf base plants of peperina minthostachys verticillata
topic Minthostachys
Somatic Embryogenesis
In Vitro Culture
Embriogénesis Somática
Cultivo in Vitro
Griseb
Peperina
url http://hdl.handle.net/20.500.12123/8145
https://link.springer.com/article/10.1007%2Fs11627-020-10098-5
https://doi.org/10.1007/s11627-020-10098-5
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