Issue 18, 2008

Engineered biosynthesis of hybrid macrolidepolyketides containing d-angolosamine and d-mycaminose moieties

Abstract

The glycosylation of natural product scaffolds with highly modified deoxysugars is often essential for their biological activity, being responsible for specific contacts to molecular targets and significantly affecting their pharmacokinetic properties. In order to provide tools for the targeted alteration of natural product glycosylation patterns, significant strides have been made to understand the biosynthesis of activated deoxysugars and their transfer. We report here efforts towards the production of plasmid-borne biosynthetic gene cassettes capable of producing TDP-activated forms of D-mycaminose, D-angolosamine and D-desosamine. We additionally describe the transfer of these deoxysugars to macrolide aglycones using the glycosyl transferases EryCIII, TylMII and AngMII, which display usefully broad substrate tolerance.

Graphical abstract: Engineered biosynthesis of hybrid macrolide polyketides containing d-angolosamine and d-mycaminose moieties

Supplementary files

Article information

Article type
Paper
Submitted
09 May 2008
Accepted
24 Jun 2008
First published
28 Jul 2008

Org. Biomol. Chem., 2008,6, 3315-3327

Engineered biosynthesis of hybrid macrolide polyketides containing D-angolosamine and D-mycaminose moieties

U. Schell, S. F. Haydock, A. L. Kaja, I. Carletti, R. E. Lill, E. Read, L. S. Sheehan, L. Low, M. Fernandez, F. Grolle, H. A. I. McArthur, R. M. Sheridan, P. F. Leadlay, B. Wilkinson and S. Gaisser, Org. Biomol. Chem., 2008, 6, 3315 DOI: 10.1039/B807914E

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