Preservation of endangered Tunisian grapevine cultivars using embryogenic cultures

The preservation of embryogenic lines derived from several endangered local grapevine cultivars was studied. Embryogenic calluses were obtained from immature anthers of eight cultivars, sampled on both fruity-cuttings and field grown vines. Anthers at the 'separated flower' stage, derived...

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Autores principales: Bouamama,Badra, Jardak,Rahma, Salem,Asma Ben, Ghorbel,Abdelwahed, Mliki,Ahmed
Lenguaje:English
Publicado: Pontificia Universidad Católica de Valparaíso 2009
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582009000200006
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spelling oai:scielo:S0717-345820090002000062009-10-20Preservation of endangered Tunisian grapevine cultivars using embryogenic culturesBouamama,BadraJardak,RahmaSalem,Asma BenGhorbel,AbdelwahedMliki,Ahmed forced anthers long-term maintenance somatic embryos Vitis vinifera The preservation of embryogenic lines derived from several endangered local grapevine cultivars was studied. Embryogenic calluses were obtained from immature anthers of eight cultivars, sampled on both fruity-cuttings and field grown vines. Anthers at the 'separated flower' stage, derived from fruity-cuttings, resulted in an increased induction of somatic embryogenesis, compared to those derived from the field. Pro-embryogenic calluses were induced on Chée and Pool (1987) basal medium, supplemented with 9 µM of 2,4-dichlorophenoxyacetic acid (2,4-D) and 11.35 µM of thidiazuron (TDZ) under dark conditions. Different anther zones (filament, abaxial, adaxial, lateral zones and entire anthers) were involved in somatic embryogenesis induction. The percentages of granular and yellowish pro-embryogenic calluses ranged between 15.6% and 34.8% in 'Kahli Kerkennah' and 'Muscat Raf-raf' cultivars, respectively. Although, morphological diversifications of pro-embryogenic calluses (several necrosis and spontaneous maturation) were observed on the induction mediumafter 5 subcultures. The reduction of 2,4-D and TDZ levels to 4.52 µM and 2.89 µM respectively, induced granular and yellowish embryogenic material. Thus, Chée and Pool (1987) (CP) enriched with 4.52 µM of 2,4-D and 2.89 µM of TDZ revealed to be the most appropriate for long-term maintenance. In fact, all the cultivars presented high and regular embryo maturation rates after 12, 24, 36 and 48 months of cultivation on this medium, under light conditions. After 4 years, they still exhibit high germination and regeneration abilities. Germination of somatic embryos was achieved on Murashige and Skoog (1962) basal-medium, with rates ranging from 69% to 96%. Only 5% of somatic embryos were concerned by morphological variations. The regenerated plantlets presented a normal phenotype under controlled greenhouse conditions, compared to mother plants.info:eu-repo/semantics/openAccessPontificia Universidad Católica de ValparaísoElectronic Journal of Biotechnology v.12 n.2 20092009-04-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582009000200006en10.4067/S0717-34582009000200006
institution Scielo Chile
collection Scielo Chile
language English
topic forced anthers
long-term maintenance
somatic embryos
Vitis vinifera
spellingShingle forced anthers
long-term maintenance
somatic embryos
Vitis vinifera
Bouamama,Badra
Jardak,Rahma
Salem,Asma Ben
Ghorbel,Abdelwahed
Mliki,Ahmed
Preservation of endangered Tunisian grapevine cultivars using embryogenic cultures
description The preservation of embryogenic lines derived from several endangered local grapevine cultivars was studied. Embryogenic calluses were obtained from immature anthers of eight cultivars, sampled on both fruity-cuttings and field grown vines. Anthers at the 'separated flower' stage, derived from fruity-cuttings, resulted in an increased induction of somatic embryogenesis, compared to those derived from the field. Pro-embryogenic calluses were induced on Chée and Pool (1987) basal medium, supplemented with 9 µM of 2,4-dichlorophenoxyacetic acid (2,4-D) and 11.35 µM of thidiazuron (TDZ) under dark conditions. Different anther zones (filament, abaxial, adaxial, lateral zones and entire anthers) were involved in somatic embryogenesis induction. The percentages of granular and yellowish pro-embryogenic calluses ranged between 15.6% and 34.8% in 'Kahli Kerkennah' and 'Muscat Raf-raf' cultivars, respectively. Although, morphological diversifications of pro-embryogenic calluses (several necrosis and spontaneous maturation) were observed on the induction mediumafter 5 subcultures. The reduction of 2,4-D and TDZ levels to 4.52 µM and 2.89 µM respectively, induced granular and yellowish embryogenic material. Thus, Chée and Pool (1987) (CP) enriched with 4.52 µM of 2,4-D and 2.89 µM of TDZ revealed to be the most appropriate for long-term maintenance. In fact, all the cultivars presented high and regular embryo maturation rates after 12, 24, 36 and 48 months of cultivation on this medium, under light conditions. After 4 years, they still exhibit high germination and regeneration abilities. Germination of somatic embryos was achieved on Murashige and Skoog (1962) basal-medium, with rates ranging from 69% to 96%. Only 5% of somatic embryos were concerned by morphological variations. The regenerated plantlets presented a normal phenotype under controlled greenhouse conditions, compared to mother plants.
author Bouamama,Badra
Jardak,Rahma
Salem,Asma Ben
Ghorbel,Abdelwahed
Mliki,Ahmed
author_facet Bouamama,Badra
Jardak,Rahma
Salem,Asma Ben
Ghorbel,Abdelwahed
Mliki,Ahmed
author_sort Bouamama,Badra
title Preservation of endangered Tunisian grapevine cultivars using embryogenic cultures
title_short Preservation of endangered Tunisian grapevine cultivars using embryogenic cultures
title_full Preservation of endangered Tunisian grapevine cultivars using embryogenic cultures
title_fullStr Preservation of endangered Tunisian grapevine cultivars using embryogenic cultures
title_full_unstemmed Preservation of endangered Tunisian grapevine cultivars using embryogenic cultures
title_sort preservation of endangered tunisian grapevine cultivars using embryogenic cultures
publisher Pontificia Universidad Católica de Valparaíso
publishDate 2009
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582009000200006
work_keys_str_mv AT bouamamabadra preservationofendangeredtunisiangrapevinecultivarsusingembryogeniccultures
AT jardakrahma preservationofendangeredtunisiangrapevinecultivarsusingembryogeniccultures
AT salemasmaben preservationofendangeredtunisiangrapevinecultivarsusingembryogeniccultures
AT ghorbelabdelwahed preservationofendangeredtunisiangrapevinecultivarsusingembryogeniccultures
AT mlikiahmed preservationofendangeredtunisiangrapevinecultivarsusingembryogeniccultures
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