TY - JOUR
T1 - Nicotiana glauca plant regeneration protocol from mesophyll protoplasts
AU - Ayala, Diana
AU - de Lourdes Torres, María
AU - Arahana, Venancio
N1 - Funding Information:
This research was financed by Consejo Nacional de Educacion Superior (CONESUP), Ecuador. We thank Robert Beatty, University of California, and Andrés Torres, Wageningen University, for critical reading of the manuscript and their valuable suggestions. Authors also thank Antonio Riofrío for helping in the development of this study. Address correspondence to Venancio Arahana at Cumbaya, Diego de Robles y Viá Interoceánica, Universidad San Francisco de Quito, Ecuador. E-mail: [email protected]
PY - 2011/1
Y1 - 2011/1
N2 - This study describes an optimization of a plant regeneration protocol from mesophyll protoplasts in N. glauca that should enable further research with this species, which has shown interesting features for plant resistance to nematodes. Protoplasts were isolated from leaf mesophyll of in vitro-grown N. glauca plants and cultured on Mprot medium supplemented with 0.45 uM 2, 4-dichlorophenoxyacetic acid 2, 4-D, 4.44 uM 6- enzylaminopurine (BAP), and 5.37 uM alpha-naphthaleneacetic acid (NAA). After five weeks, microcalli were subcultured individually in MS medium supplemented with 0.27 uM NAA and 17.76 uM BAP for shoot regeneration. The 0.5 cm high shoots that appeared after eight weeks were transferred to MS medium without plant growth regulators for root induction. Plant acclimatization began 18 weeks after protoplast isolation and lasted for three weeks, after which they were transferred to soil. Shoot regeneration efficiency was 80-90%, and rooting efficiency was 86%.
AB - This study describes an optimization of a plant regeneration protocol from mesophyll protoplasts in N. glauca that should enable further research with this species, which has shown interesting features for plant resistance to nematodes. Protoplasts were isolated from leaf mesophyll of in vitro-grown N. glauca plants and cultured on Mprot medium supplemented with 0.45 uM 2, 4-dichlorophenoxyacetic acid 2, 4-D, 4.44 uM 6- enzylaminopurine (BAP), and 5.37 uM alpha-naphthaleneacetic acid (NAA). After five weeks, microcalli were subcultured individually in MS medium supplemented with 0.27 uM NAA and 17.76 uM BAP for shoot regeneration. The 0.5 cm high shoots that appeared after eight weeks were transferred to MS medium without plant growth regulators for root induction. Plant acclimatization began 18 weeks after protoplast isolation and lasted for three weeks, after which they were transferred to soil. Shoot regeneration efficiency was 80-90%, and rooting efficiency was 86%.
KW - Calli
KW - Cpw medium
KW - In vitro culture
KW - Protoplasts
UR - https://www.scopus.com/pages/publications/79951994935
U2 - 10.1080/15427528.2011.518303
DO - 10.1080/15427528.2011.518303
M3 - Artículo
AN - SCOPUS:79951994935
SN - 1542-7528
VL - 25
SP - 1
EP - 10
JO - Journal of Crop Improvement
JF - Journal of Crop Improvement
IS - 1
ER -