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FAIR-CT97-3628
Improving production and quality of essential oil from aromatic plants by genetic engineering |
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Type of Project | Shared Cost |
| Contract No | FAIR-CT97-3628 | |
| Total Cost | 644,180 ECU | |
| EC Contribution | 549,844 ECU | |
| Start Date | 01/04/1998 | |
| Duration | 36 Months |
Improving production and quality of essential oil from aromatic plants by genetic engineering
Objectives
Plant secondary metabolites are extensively used as flavours, fragrances, pigments and medicines by the food and pharmaceutical industries. Even with contemporary advances in synthetic organic chemistry, plants are the main source of over 25 per cent of all prescription medicines. Availability and quality of raw material depend on climatic factors, sacristy of the species, and geography of the area of plant growth that can sometimes include remote and politically unstable regions. Clearly the cultivation of such species must be encouraged and this depends also on the existence of commercially competitive genotypes. Secondary metabolite accumulation in tissue or cell cultures of most plant species is usually orders of magnitude lower than that in the intact plant. Transcriptional inactivation of key regulatory genes of secondary metabolism has been postulated to take place in cultured tissues. As long as the mechanism of inactivation remains unknown significant progress in the field of biotechnology for in vitro secondary metabolite production will be slow depending on accidental mutations resulting in overproducing somaclones.
Technical Approach
Rose essential oil production has been chosen as the model system because of the relative simplicity of the biosynthetic pathway, the easy identification of the oil ingredients, and the commercial interest in this species. Rose oil contains monoterpenes used extensively in the cosmetics industry. Their synthesis as well as that of other secondary metabolites, is affected by biotic and abiotic stresses. Potential second messengers, common to the signal transduction pathways of the various inducing treatments, are free radicals, lipid peroxides, and their derivatives.
The specific objectives are:
Results To Date
A protocol yielding high quality rose DNA (gDNA) was developed. The gDNA was used in southern blots, for the gDNA library construction, and in PCRs using degenerate HMGR primers. The PCR products are being cloned prior to sequencing. Total petal RNA was extracted for use in the cDNA library construction, and tissue specific northern blots. Protocols for the evaluation of terpenoid content in minimal petal masses are under development. Callus cultures have been established from 3 reference strains. Familiarisation with the yeast 2-hybrid system is in progress.
Contacts
Coordinator
EC Scientific Officer
Participant
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by CPL Press:
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