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Elucidation of the unusual methylenomycin biosynthetic pathway in Streptomyces coelicolor

Reference	BB/E008003/1
Principal Investigator / Supervisor	Professor Gregory Challis
Co-Investigators / Co-Supervisors	Dr Christophe Corre
Institution	University of Warwick
Department	Chemistry
Funding type	Research
Value (£)	318,860
Status	Completed
Type	Research Grant
Start date	01/11/2006
End date	31/10/2009
Duration	36 months

Abstract

The methylenomycins are an unusual group of cyclopentanoid antibiotics produced by Streptomyces species. They possess a broad spectrum of activity against Gram-positive bacteria and some Gram negative strains, as well as antitumour activity against Lewis lung carcinoma. The sequence of the mmy gene cluster, which directs methylenomycin biosynthesis in S. coelicolor, recently became available as a result of a BBSRC-funded project to determine the complete sequence of the giant linear plasmid SCP1. Analysis of the enzymes encoded by this cluster indicates that the pathway for methylenomycin biosynthesis is highly unusual. In parallel work it has been shown that the carbon atoms of the methylenomycins are derived from a unique combination of primary metabolic precursors - acetyl CoA, malonyl CoA and a pentulose. This project aims to elucidate the intermediates on the pathway for methylenomycin biosynthesis, the reactions that give rise to these intermediates, and the enzymes that catalyse these reactions. A variety of approaches will be utilised in this multidisciplinary project including comparative metabolic profiling of biosynthetic mutants and wild type S. coelicolor to identify accumulated metabolites and feeding of isotopically labelled precursors to establish linkage between the metabolites accumulated and the methylenomycin biosynthetic pathway. The genetic engineering of the methylenomycin biosynthetic pathway to generate novel derivatives of the antibiotics will also be explored. The output of this project will be fundamental new insights into pathways for antibiotic biosynthesis in microorganisms which may ultimately lead to the discovery of new mechanistic enzymology for complex natural product biosynthesis, novel biocatalysts for biotransformation of highly functionalised organic molecules and the knowledge required to rationally engineer the methylenomycin biosynthetic pathway to produce new antibiotics.

Summary

There is an urgent need for improved and new antibiotics due to the increasing emergence of multi-drug resistant pathogens such as vancomycin and methicillin resistant Staphylococcus aureus (VMRSA). One approach to meeting this need is the engineering of natural synthetic (biosynthetic) pathways to antibiotics in producing organisms to generate novel derivatives with potentially superior properties for medical applications. Fundamental knowledge of the genes, enzymes, intermediates and reactions involved in antibiotic biosynthetic pathways is an essential prerequisite for biosynthetic pathway engineering. Methylenomycins belong to an unusual group of antibiotics that have a broad spectrum of activity against Gram-positive and Gram-negative bacteria. Recently the genes required for assembly of the methylenomycins in the microorganism Streptomyces coelicolor have been identified and it has been shown that the methylenomycins are assembled from a unique combination of molecular building blocks. Analysis of the enzymes encoded by the biosynthetic genes indicates that the pathway for methylenomycin biosynthesis is highly novel and does not show similarities to the known pathways for biosynthesis of other antibiotics. This research project aims to investigate the unique methylenomycin biosynthetic pathway by identifying and determining the molecular structure of intermediates on the pathway and examining the role of each of the biosynthetic genes and enzymes. The potential for engineering the pathway to produce novel derivatives of the methylenomycins will also be explored.

Committee	Closed Committee - Plant & Microbial Sciences (PMS)
Research Topics	Industrial Biotechnology, Microbiology
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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