Norway spruce somatic embryogenesis: high-frequency initiation from light-cultured mature embryos
Author(s) -
Shirley A. Verhagen,
Steven R. Wann
Publication year - 1989
Publication title -
plant cell tissue and organ culture (pctoc)
Language(s) - English
Resource type - Journals
eISSN - 1573-5044
pISSN - 0167-6857
DOI - 10.1007/bf00036518
Subject(s) - somatic embryogenesis , biology , hypocotyl , callus , botany , embryo , explant culture , murashige and skoog medium , embryogenesis , microbiology and biotechnology , in vitro , genetics
Somatic embryos and rooted plantlets have been regenerated from light-initiated embryogenic callus derived from mature embryos of Picea abies. Under a 16 h photoperiod, mature zygotic embryos were cultured on a modified half-strength Murashige & Skoog medium without NH4NO3 and supplemented with 5 mM glutamine, 4.5 µM N6-benzyladenine and 10.7 µM naphthaleneacetic acid or 10 µM 2,4-dichlorophenoxyacetic acid. White translucent embryogenic callus, proliferating from the callusing hypocotyl region after 3 weeks incubation, was isolated from the green non-embryogenic tissue and subcultured for over 12 months. Upon transfer of the embryogenic callus through a specific sequence of media, somatic embryos proceeded to mature, elongating and forming rings of cotyledonary leaves similar to those of zygotic embryos. Transferred to medium without growth regulators, the somatic embryos ‘germinated’ and produced plantlets with green cotyledons, elongated hypocotyls and primary roots.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom