1School of Biotechnology & Genetic Engineering, Bharathiar University, Coimbatore-641 046
2Department of Biotechnology, Sri Padmavati Mahila Visva Vidyalayam, Tirupati-517 502
3PET Research Foundation, Department of ChemistryUniversity of Mysore, PESCE, Mandya-571 401
Department of Crop Physiology, Acharya N.G. Ranga Agricultural University, Naira-532185, India
*Corresponding author's e-mail: pesmurari@gmail.com
Online published on 30 April, 2016.
An efficient regeneration was developed using mature and immature embryos by using Maize (Zea mays L) variety MU 2092. Mature embryos are removed from surface sterilized seeds, slice them into halves and immature embryos are detached from seed endosperm. Both are used as explants to initiate callus on N6 medium supplemented with 2, 4 D @ 4.0 mg. L−1. The induction frequency of primary calli i.e embryogenic callus was 90% in maize. The embryogenic calli on N6 medium supplemented with 6-benzylaminopurine (BAP) @ 0.5 mg. L−1 and kinetin @ 0.5 mg. L−1 was more effective in producing shoots. The culture expressed maximum plant regeneration potential with eight shoots per embryo on regeneration. Green shoots thus developed were successfully rooted within 20 days on MS media containing IBA (Indole-3-Butyric acid) 1mg L−1. Over 86% of rooted plants grew well and produced seeds normally when transferred to green house. The important advantage of this improved method is shortening of regeneration time by providing an efficient and rapid regeneration tool for mature and immature embryos.
Embryogenic callus-Maize (Zea mays L), Mature embryo, Immature embryo, Plant regeneration