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Early Steps in Alkaloid Biosynthesis
Reference
BBS/E/J/000CY117
Principal Investigator / Supervisor
Professor Sarah O'Connor
Co-Investigators /
Co-Supervisors
Institution
John Innes Centre
Department
John Innes Centre Department
Funding type
Research
Value (£)
6,043
Status
Completed
Type
Institute Project
Start date
01/07/2011
End date
28/02/2013
Duration
20 months
Abstract
Understanding the enzymes that catalyze natural product biosynthesis may enable production inmore tractable host organisms, and may also allow reprogramming of biosynthetic pathways to produce "unnatural" natural products with potentially improved pharmacological activities. Many biosynthetic pathways of natural products found in higher plants remain largely uncharacterized. Our laboratory seeks to understand, and ultimately harness, the metabolic pathways that direct the biosynthesis of plant-derived terpene indole alkaloids. This family of natural products, which comprises approximately 3000 members, is a particularly diverse group of molecules with a range of chemical structures and medicinal uses. We propose to study the mechanism of the few enzymes that have been cloned, isolate and clone as yet uncharacterized enzymes, and determine whether these enzymes can accept alternate substrates that would yield novel alkaloid structures. Short term efforts are currently focus on the mechanism of the first two enzymes of the pathway (strictosidine synthase and strictosidine glucosidase) and determine whether these enzymes can utilize alternate substrates that result in modified alkaloid structures. Understanding the mechanism of these enzymes may also provide clues as to how to modulate substrate specificity. Longer term efforts will focus on identifying a downstream enzyme that immediately follows strictosidine glucosidase in the pathway, and that plays a role in controlling the divergence from the corynanthe type alkaloids to the more complex Iboga and Aspidosperma alkaloids. Harnessing this complex metabolic pathway may enable the economical production of valuable medicinal compounds and allow nature's biosynthetic machinery to be hijacked for the production of unnatural alkaloids of our own design.
Summary
unavailable
Committee
Not funded via Committee
Research Topics
Industrial Biotechnology, Plant Science, Structural Biology, Synthetic Biology
Research Priority
X – Research Priority information not available
Research Initiative
X - not in an Initiative
Funding Scheme
X – not Funded via a specific Funding Scheme
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