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Analysis and Refactoring of the A-74528 Biosynthetic Pathway.

Authors :
Fitzgerald, Jay T.
Charkoudian, Louise K.
Watts, Katharine R.
Khosla, Chaitan
Source :
Journal of the American Chemical Society. 3/13/2013, Vol. 135 Issue 10, p3752-3755. 4p.
Publication Year :
2013

Abstract

A-74528 is a C30 polyketide natural product that functions as an inhibitor of 2′,5′-oligoadenylate phosphodiesterase (2′-PDE), a key regulatory enzyme of the interferon pathway. Modulation of 2′-PDE represents a unique therapeutic approach for regulating viral infections. The gene cluster responsible for biosynthesis of A-74528 yields minute amounts of this natural product together with considerably larger quantities of a structurally dissimilar C30 cytotoxic agent, fredericamycin. Through construction and analysis of a series of knockout mutants, we identified the genes necessary for A-74528 biosynthesis. Remarkably, the formation of six stereocenters and the regiospecific formation of six rings in A-74528 appear to be catalyzed by only two tailoring enzymes, a cyclase and an oxygenase, in addition to the core polyketide synthase. The inferred pathway was genetically refactored in a heterologous host, Streptomyces coelicolor CH999, to produce 3 mg/L A-74528 in the absence of fredericamycin. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00027863
Volume :
135
Issue :
10
Database :
Academic Search Index
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
86667479
Full Text :
https://doi.org/10.1021/ja311579s