Ether bridge formation in loline alkaloid biosynthesis.
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| Abstract | :  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. | 
| Year of Publication | :  2014 | 
| Journal | :  Phytochemistry | 
| Volume | :  98 | 
| Number of Pages | :  60-8 | 
| ISSN Number | :  0031-9422 | 
| URL | :  https://linkinghub.elsevier.com/retrieve/pii/S0031-9422(13)00450-0 | 
| DOI | :  10.1016/j.phytochem.2013.11.015 | 
| Short Title | :  Phytochemistry | 
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