Abstract
Homozygosity was induced in transgenic barley by microspore culture.
Spikes of transgenic barley plants carrying microspores in the late
uni-nucleate stage were cold pretreated. Teflon rod maceration and a
density of 100 000 viable micropores per plate were used. The developed
calli were regenerated and plantlets were treated with colchicine. The
microspore culture of 16 mother plants (three transgenic lines) resulted
in 927 green regenerants. Of these plants, 476 were transferred to
soil, 380 were transgenic, 358 reached maturity and 350 were fertile
with a normal seed-set carrying a yield of 6.9 kg. A production
efficiency of 0.8 fertile transgenic doubled haploid barley plants per
spike used for microspore isolation was recorded. The produced
transgenic seeds were used in malting experiments.
Original language | English |
---|---|
Pages (from-to) | 601 - 609 |
Number of pages | 9 |
Journal | Acta Physiologiae Plantarum |
Volume | 27 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2005 |
MoE publication type | A1 Journal article-refereed |
Keywords
- barley
- double haploid
- endo-beta-glucanase
- microspore culture
- transgenic