Efficient and stable regeneration from protoplasts of Cyclamen coum Miller via somatic embryogenesis

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)171-182
Seitenumfang12
FachzeitschriftPlant Cell, Tissue and Organ Culture
Jahrgang101
Ausgabenummer2
PublikationsstatusVeröffentlicht - 4 Feb. 2010

Abstract

Embryogenic cultures of Cyclamen coum were established on solid media and in suspension, and their growth characteristics in response to different concentrations of plant growth regulators (PGRs) were evaluated. Embryogenic cultures exhibited a high regeneration capacity of 876 somatic embryos per gram fresh mass. Up to 4.24 × 105 protoplasts per gram of fresh mass were isolated from somatic embryos and embryogenic suspension cultures. Protoplasts derived from both embryos and suspension cultures were successfully cultured in vitro and regenerated into plants via somatic embryogenesis. Phenotypic analyses and flow cytometric measurements revealed that some regenerated plants were tetraploid. About 20% of the protoplast-derived calluses used for regeneration were tetraploid, while tetraploidy was found in 0.9% of the plants regenerated from the embryogenic cultures.

ASJC Scopus Sachgebiete

  • Agrar- und Biowissenschaften (insg.)
  • Gartenbau

Zitieren

Efficient and stable regeneration from protoplasts of Cyclamen coum Miller via somatic embryogenesis. / Prange, Anika Nadja Sabine; Serek, Margrethe; Bartsch, Melanie et al.
in: Plant Cell, Tissue and Organ Culture, Jahrgang 101, Nr. 2, 04.02.2010, S. 171-182.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Prange, Anika Nadja Sabine ; Serek, Margrethe ; Bartsch, Melanie et al. / Efficient and stable regeneration from protoplasts of Cyclamen coum Miller via somatic embryogenesis. in: Plant Cell, Tissue and Organ Culture. 2010 ; Jahrgang 101, Nr. 2. S. 171-182.
Download
@article{98de7b77f6c943eea311990f143761a2,
title = "Efficient and stable regeneration from protoplasts of Cyclamen coum Miller via somatic embryogenesis",
abstract = "Embryogenic cultures of Cyclamen coum were established on solid media and in suspension, and their growth characteristics in response to different concentrations of plant growth regulators (PGRs) were evaluated. Embryogenic cultures exhibited a high regeneration capacity of 876 somatic embryos per gram fresh mass. Up to 4.24 × 105 protoplasts per gram of fresh mass were isolated from somatic embryos and embryogenic suspension cultures. Protoplasts derived from both embryos and suspension cultures were successfully cultured in vitro and regenerated into plants via somatic embryogenesis. Phenotypic analyses and flow cytometric measurements revealed that some regenerated plants were tetraploid. About 20% of the protoplast-derived calluses used for regeneration were tetraploid, while tetraploidy was found in 0.9% of the plants regenerated from the embryogenic cultures.",
keywords = "Flow cytometry, Ornamental plant, Ploidy stability, Protoplast isolation, Somaclonal variation, Vegetative propagation",
author = "Prange, {Anika Nadja Sabine} and Margrethe Serek and Melanie Bartsch and Traud Winkelmann",
note = "Funding Information: Acknowledgments The authors thank Frank Schaarschmidt for his excellent guidance in the statistical data analysis. The financial support of the German Federal Ministry of Economics and Technology through the program PRO INNO grant no. KF0054802MD5 is gratefully acknowledged.",
year = "2010",
month = feb,
day = "4",
doi = "10.1007/s11240-010-9674-z",
language = "English",
volume = "101",
pages = "171--182",
journal = "Plant Cell, Tissue and Organ Culture",
issn = "0167-6857",
publisher = "Springer Netherlands",
number = "2",

}

Download

TY - JOUR

T1 - Efficient and stable regeneration from protoplasts of Cyclamen coum Miller via somatic embryogenesis

AU - Prange, Anika Nadja Sabine

AU - Serek, Margrethe

AU - Bartsch, Melanie

AU - Winkelmann, Traud

N1 - Funding Information: Acknowledgments The authors thank Frank Schaarschmidt for his excellent guidance in the statistical data analysis. The financial support of the German Federal Ministry of Economics and Technology through the program PRO INNO grant no. KF0054802MD5 is gratefully acknowledged.

PY - 2010/2/4

Y1 - 2010/2/4

N2 - Embryogenic cultures of Cyclamen coum were established on solid media and in suspension, and their growth characteristics in response to different concentrations of plant growth regulators (PGRs) were evaluated. Embryogenic cultures exhibited a high regeneration capacity of 876 somatic embryos per gram fresh mass. Up to 4.24 × 105 protoplasts per gram of fresh mass were isolated from somatic embryos and embryogenic suspension cultures. Protoplasts derived from both embryos and suspension cultures were successfully cultured in vitro and regenerated into plants via somatic embryogenesis. Phenotypic analyses and flow cytometric measurements revealed that some regenerated plants were tetraploid. About 20% of the protoplast-derived calluses used for regeneration were tetraploid, while tetraploidy was found in 0.9% of the plants regenerated from the embryogenic cultures.

AB - Embryogenic cultures of Cyclamen coum were established on solid media and in suspension, and their growth characteristics in response to different concentrations of plant growth regulators (PGRs) were evaluated. Embryogenic cultures exhibited a high regeneration capacity of 876 somatic embryos per gram fresh mass. Up to 4.24 × 105 protoplasts per gram of fresh mass were isolated from somatic embryos and embryogenic suspension cultures. Protoplasts derived from both embryos and suspension cultures were successfully cultured in vitro and regenerated into plants via somatic embryogenesis. Phenotypic analyses and flow cytometric measurements revealed that some regenerated plants were tetraploid. About 20% of the protoplast-derived calluses used for regeneration were tetraploid, while tetraploidy was found in 0.9% of the plants regenerated from the embryogenic cultures.

KW - Flow cytometry

KW - Ornamental plant

KW - Ploidy stability

KW - Protoplast isolation

KW - Somaclonal variation

KW - Vegetative propagation

UR - http://www.scopus.com/inward/record.url?scp=77952009111&partnerID=8YFLogxK

U2 - 10.1007/s11240-010-9674-z

DO - 10.1007/s11240-010-9674-z

M3 - Article

AN - SCOPUS:77952009111

VL - 101

SP - 171

EP - 182

JO - Plant Cell, Tissue and Organ Culture

JF - Plant Cell, Tissue and Organ Culture

SN - 0167-6857

IS - 2

ER -