Abstract
We compared the ability of different plant-based
expression platforms to produce geraniol, a key
metabolite in the monoterpenoid branch of the terpenoid
indole alkaloid biosynthesis pathway. A geraniol synthase
gene isolated from Valeriana officinalis (VoGES) was
stably expressed in different tobacco systems. Intact
plants were grown in vitro and in the greenhouse and were
used to generate cell suspension and hairy root cultures.
VoGES was also transiently expressed in N. benthamiana.
The highest geraniol content was produced by intact
transgenic plants grown in vitro (48 µg/g fresh weight,
fw), followed by the transient expression system (27 µg/g
fw), transgenic plants under hydroponic conditions in the
greenhouse and cell suspension cultures (16 µg/g fw), and
finally hairy root cultures (9 µg/g fw). Differences in
biomass production and the duration of cultivation
resulted in a spectrum of geraniol productivities. Cell
suspension cultures achieved a geraniol production rate
of 1.8 µg/g fresh biomass per day, whereas transient
expression produced 5.9 µg/g fresh biomass per day (if
cultivation prior to agroinfiltration is ignored) or 0.5
µg/g fresh biomass per day (if cultivation prior to
agroinfiltration is included). The superior productivity,
strict process control and simple handling procedures
available for transgenic cell suspension cultures suggest
that cells are the most promising system for further
optimization and ultimately for the scaled-up production
of geraniol
Original language | English |
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Pages (from-to) | 373-380 |
Journal | Plant Cell, Tissue and Organ Culture |
Volume | 117 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2014 |
MoE publication type | A1 Journal article-refereed |
Keywords
- Cell suspension cultures
- geraniol synthase
- hydroponics
- tobacco plants
- Valeriana officinalis