Ether bridge formation in loline alkaloid biosynthesis.

Phytochemistry

Department of Plant Pathology, 201F Plant Sciences Building, 1405 Veterans Drive, University of Kentucky, Lexington, KY 40546-0312, USA. Electronic address:

Published: February 2014

Lolines are potent insecticidal agents produced by endophytic fungi of cool-season grasses. These alkaloids are composed of a pyrrolizidine ring system and an uncommon ether bridge linking carbons 2 and 7. Previous results indicated that 1-aminopyrrolizidine was a pathway intermediate. We used RNA interference to knock down expression of lolO, resulting in the accumulation of an alkaloid identified as exo-1-acetamidopyrrolizidine based on high-resolution MS and NMR. Genomes of endophytes differing in alkaloid profiles were sequenced, revealing that those with mutated lolO accumulated exo-1-acetamidopyrrolizidine but no lolines. Heterologous expression of wild-type lolO complemented a lolO mutant, resulting in the production of N-acetylnorloline. These results indicated that the non-heme iron oxygenase, LolO, is required for ether bridge formation, probably through oxidation of exo-1-acetamidopyrrolizidine.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929955PMC
http://dx.doi.org/10.1016/j.phytochem.2013.11.015DOI Listing

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