Production of pharmaceutics in daffodils: biological factors influencing the content of galanthamine alkaloid

Lead Research Organisation: University of Liverpool
Department Name: Sch of Biological Sciences

Abstract

This project addresses the production of the alkaloid galanthamine within daffodils, as a novel crop for industrial production of a medication approved by NICE for treatment of moderate Alzheimer's Disease. There are an estimated 700,000 people at different stages of dementia in the UK, providing a demand for treatments. Galanthamine is an isoquinoline alkaloid with acetylcholine esterase inhibition properties. It is one of over 500 alkaloids, several with proven pharmacological activity, produced by species within the Amaryllidaceae. Current commercial production utilises mainly wild Galanthus sp. (snowdrops), Leucojum sp. or waste from horticultural Narcissus sp. (daffodils) production. The commercial objective of the SME industrial partner, Alzeim Ltd, is to optimise production and extraction of galanthamine from daffodils. Methods for large-scale daffodil cultivation in the UK have been geared to horticultural flower production. Following development of improved chemical engineering methods for extraction, purification and quality control of galanthamine from daffodil leaves, there is now a need to understand the biological side of the process. Initial work by the company has indicated that galanthamine levels are higher in daffodils grown in upland regions rather than lowland agricultural conditions. This indicates that production may be a response to abiotic stress. The academic partners at the University of Liverpool have research interests and experience with plant stress responses, secondary metabolite production and genomics. There is very little information on the levels of galanthamine during the daffodil life-cycle or in different plant organs. Knowledge of these basic parameters of plant physiology is required to optimise the agronomy of daffodils for galanthamine production. The consequences of abiotic stresses (fertilizer, agrochemicals, elicitors, physical damage) on galanthamine levels will be examined in laboratory and field plots. Confirmation of differential levels of galanthamine in cultivars that have already undergone a preliminary screen will open the way to obtaining data on the biosynthetic pathway and its regulation. There has been extensive interest in the total chemical synthesis of Amaryllidaceae alkaloids and a biosynthetic pathway has been inferred from these studies. It is presumed to follow a series of modifications to norbelladine after its formation from the aromatic aminoacids tyrosine and phenylalanine. The biosynthetic enzymes are unknown, but are of considerable interest since detection of their mRNA by PCR, or gene expression markers associated with high galanthamine, should provide a sensitive reporter of galanthamine biosynthesis. Next generation sequencing technologies will provide the resources for discovery of genes potentially associated with high galanthamine production or implicated in the pathway. A comparison of the transcriptome of daffodil tissues with high and low galanthamine production, obtained using 454 pyrosequencing, should highlight components of this pathway, regulatory components or associated markers. This will be used to develop a high-throughput chemical screen for galanthamine induction and a simple QPCR based assay for high galanthamine production. In addition, the enzymes themselves may have value as novel biocatalysts since they will carry out unusual stereospecific reactions. It will also provide information on the biosynthesis of other alkaloids within the daffodil tissues, providing the basis for a systems approach to the biosynthesis of Amaryllidaceae alkaloids. This project therefore provides a combination of essential underpinning plant physiology to support the commercial objectives of the SME Alzeim Ltd and novel science to advance understanding of alkaloid biosynthesis.

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