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Generation of Alkaloid Diversity Using Biocatalysts
Reference
BBS/E/J/000CA489
Principal Investigator / Supervisor
Professor Sarah O'Connor
Co-Investigators /
Co-Supervisors
Institution
John Innes Centre
Department
John Innes Centre Department
Funding type
Research
Value (£)
45,888
Status
Completed
Type
Institute Project
Start date
03/12/2012
End date
30/11/2015
Duration
35 months
Abstract
The enzymes responsible for the biosynthesis of natural products represent a phenomenal starting point for mechanistic and engineering studies. In this proposal we use enzyme engineering as both a tool to understand mechanism and as a means to generate enzymes with new catalytic activities. General Objectives - Collectively, the experiments described in this proposal will enable the generation of a broad base of biocatalysts that will catalyse the stereoselective production of a variety of beta-carbolines, a chemical scaffold widely used in pharmaceuticals. The work will also provide a mechanistic framework to understand the mode of stereoselectivity in other enzymes. We focus on the Pictet-Spenglerase from indole alkaloid biosynthesis, strictosidine synthase, as well as several halogenases that catalyse chlorination of indoles.
Summary
unavailable
Committee
Not funded via Committee
Research Topics
Industrial Biotechnology, Structural 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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