Role of the LolP cytochrome P450 monooxygenase in loline alkaloid biosynthesis.
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| Abstract | :  The insecticidal loline alkaloids, produced by Neotyphodium uncinatum and related endophytes, are exo-1-aminopyrrolizidines with an ether bridge between C-2 and C-7. Loline alkaloids vary in methyl, acetyl, and formyl substituents on the 1-amine, which affect their biological activity. Enzymes for key loline biosynthesis steps are probably encoded by genes in the LOL cluster, which is duplicated in N. uncinatum, except for a large deletion in lolP2. The role of lolP1 was investigated by its replacement with a hygromycin B phosphotransferase gene. Compared to wild type N. uncinatum and an ectopic transformant, DeltalolP1 cultures had greatly elevated levels of N-methylloline (NML) and lacked N-formylloline (NFL). Complementation of DeltalolP1 with lolP1 under control of the Emericella nidulans trpC promoter restored NFL production. These results and the inferred sequence of LolP1 indicate that it is a cytochrome P450, catalyzing oxygenation of an N-methyl group in NML to the N-formyl group in NFL. | 
| Year of Publication | :  2008 | 
| Journal | :  Fungal genetics and biology : FG & B | 
| Volume | :  45 | 
| Issue | :  9 | 
| Number of Pages | :  1307-14 | 
| ISSN Number | :  1087-1845 | 
| URL | :  https://linkinghub.elsevier.com/retrieve/pii/S1087-1845(08)00112-6 | 
| DOI | :  10.1016/j.fgb.2008.07.001 | 
| Short Title | :  Fungal Genet Biol | 
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