Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture
Plant regeneration was induced with 40 and 400-day-old leaf explant derived callus from tetraploid (2n = 24) Tradescantia crassifoilia Cav. Schenk & Hildebrandt medium supplemented with 0.8 mg · 1−1 2,4-D + 0.1 mg · 1−1 Kin was the most suitable combination for callus induction. Shoot regene...
Guardado en:
Autores principales: | , , , |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_01761617_v119_n5_p467_Escandon |
Aporte de: |
id |
todo:paper_01761617_v119_n5_p467_Escandon |
---|---|
record_format |
dspace |
spelling |
todo:paper_01761617_v119_n5_p467_Escandon2023-10-03T15:08:01Z Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture Escandón, A. Martínez, A. Caso, O.H. Pomar, M.C. 2,4-D 2,4-Dichlorophenoxyacetic acid 6-benzylaminopurine 6-fufuryl aminopurine alphanaphthaleneacetic acid aneuploid plants BAP callus culture Kin NAA regenerants Tradescantia crassifolia Plant regeneration was induced with 40 and 400-day-old leaf explant derived callus from tetraploid (2n = 24) Tradescantia crassifoilia Cav. Schenk & Hildebrandt medium supplemented with 0.8 mg · 1−1 2,4-D + 0.1 mg · 1−1 Kin was the most suitable combination for callus induction. Shoot regeneration was achieved in the same medium, but with either 0.5 to 2.0 mg · 1−1 BAP or with a combination of 0.01 mg · 1−1 of NAA plus from 0.1 to 5.0 mg - 1−1 of BAP. The chromosome number both in the calli and in the roots differentiated from them in the 40-day-old calli (2 subcultures) was 2n = 24. However in the 400-day-old tissue (20 subcultures) only chromosome counts of 2n = 21 were obtained in the calli and in the differentiated roots. Also 2n = 20, 21 and 42 were counted in 17 regenerants from 400-day-old calli. The most frequent chromosome number in the latter (15 individuals) was 2n = 21. © 1985, Gustav Fischer Verlag, Stuttgart. All rights reserved. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01761617_v119_n5_p467_Escandon |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
2,4-D 2,4-Dichlorophenoxyacetic acid 6-benzylaminopurine 6-fufuryl aminopurine alphanaphthaleneacetic acid aneuploid plants BAP callus culture Kin NAA regenerants Tradescantia crassifolia |
spellingShingle |
2,4-D 2,4-Dichlorophenoxyacetic acid 6-benzylaminopurine 6-fufuryl aminopurine alphanaphthaleneacetic acid aneuploid plants BAP callus culture Kin NAA regenerants Tradescantia crassifolia Escandón, A. Martínez, A. Caso, O.H. Pomar, M.C. Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture |
topic_facet |
2,4-D 2,4-Dichlorophenoxyacetic acid 6-benzylaminopurine 6-fufuryl aminopurine alphanaphthaleneacetic acid aneuploid plants BAP callus culture Kin NAA regenerants Tradescantia crassifolia |
description |
Plant regeneration was induced with 40 and 400-day-old leaf explant derived callus from tetraploid (2n = 24) Tradescantia crassifoilia Cav. Schenk & Hildebrandt medium supplemented with 0.8 mg · 1−1 2,4-D + 0.1 mg · 1−1 Kin was the most suitable combination for callus induction. Shoot regeneration was achieved in the same medium, but with either 0.5 to 2.0 mg · 1−1 BAP or with a combination of 0.01 mg · 1−1 of NAA plus from 0.1 to 5.0 mg - 1−1 of BAP. The chromosome number both in the calli and in the roots differentiated from them in the 40-day-old calli (2 subcultures) was 2n = 24. However in the 400-day-old tissue (20 subcultures) only chromosome counts of 2n = 21 were obtained in the calli and in the differentiated roots. Also 2n = 20, 21 and 42 were counted in 17 regenerants from 400-day-old calli. The most frequent chromosome number in the latter (15 individuals) was 2n = 21. © 1985, Gustav Fischer Verlag, Stuttgart. All rights reserved. |
format |
JOUR |
author |
Escandón, A. Martínez, A. Caso, O.H. Pomar, M.C. |
author_facet |
Escandón, A. Martínez, A. Caso, O.H. Pomar, M.C. |
author_sort |
Escandón, A. |
title |
Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture |
title_short |
Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture |
title_full |
Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture |
title_fullStr |
Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture |
title_full_unstemmed |
Regeneration of Aneuploid Plants from Tetraploid (2n = 24) Tradescantia crassifolia Cav. through Callus Culture |
title_sort |
regeneration of aneuploid plants from tetraploid (2n = 24) tradescantia crassifolia cav. through callus culture |
url |
http://hdl.handle.net/20.500.12110/paper_01761617_v119_n5_p467_Escandon |
work_keys_str_mv |
AT escandona regenerationofaneuploidplantsfromtetraploid2n24tradescantiacrassifoliacavthroughcallusculture AT martineza regenerationofaneuploidplantsfromtetraploid2n24tradescantiacrassifoliacavthroughcallusculture AT casooh regenerationofaneuploidplantsfromtetraploid2n24tradescantiacrassifoliacavthroughcallusculture AT pomarmc regenerationofaneuploidplantsfromtetraploid2n24tradescantiacrassifoliacavthroughcallusculture |
_version_ |
1807322461848469504 |