Abstract
In vitro plant regeneration of Gentiana macrophylla Pall. and determination of gentiopicroside content during somatic embryogenesis are
described in the present work. The highest percentage of embryogenic callus formation
was observed in Murashige and Skoog (MS) medium supplemented with 1.0 mg/L 2,4-dichlorophenoxyacetic
acid (2,4-D) and 1.0 mg/L 6-benzylaminopurine (BA). Calli were subcultured on MS medium
containing 1.0 mg/L 2,4-D, 1.0 mg/L BA and 500 mg/L lactalbumin hydrolysate (LH) at
intervals of 25 days. A higher frequency of somatic embryo maturation was achieved
on MS medium containing B5 vitamins (MB) supplemented with different concentrations
of 1-naphthaleneacetic acid (NAA) and BA than with a combination of NAA and kinetin
(KT). Addition of AgNO3 improved maturation of somatic embryos while thidiazuron (TDZ) promoted vitrification.
The gentiopicroside contents of embryogenic calli and globular-, heart-, torpedo-,
and cotyledon-shaped embryoids were determined by high-performance liquid chromatography
(HPLC). Gentiopicroside was not detectable in embryogenic calli, but in all types
of somatic embryos. The highest gentiopicroside content was observed in cotyledon-shaped
embryoids, reaching more than 12 mg/g dry weight.
Key words
Gentianaceae -
Gentiana macrophylla
- gentiopicroside - HPLC - secondary metabolites - somatic embryo
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1 These authors made equal contributions to this work.
Zi-Qin Xu
Institute of Life Science Northwest University
Taibaibeilu 229
Xi'an
710069 Shaanxi
People's Republic of China
Phone: + 86 29 88 30 34 84
Email: ziqinxu@nwu.edu.cn