Structure revision of cryptosporioptides and determination of the genetic basis for dimeric xanthone biosynthesis in fungi† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc05126g

Three novel dimeric xanthones, cryptosporioptides A–C were isolated from Cryptosporiopsis sp. 8999 and their structures elucidated. Three novel dimeric xanthones, cryptosporioptides A–C were isolated from Cryptosporiopsis sp. 8999 and their structures elucidated. Methylation of cryptosporioptide A g...

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Bibliographic Details
Published in:Chemical science (Cambridge) Vol. 10; no. 10; pp. 2930 - 2939
Main Authors: Greco, Claudio, de Mattos-Shipley, Kate, Bailey, Andrew M., Mulholland, Nicholas P., Vincent, Jason L., Willis, Christine L., Cox, Russell J., Simpson, Thomas J.
Format: Journal Article
Language:English
Published: Royal Society of Chemistry 21-01-2019
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Summary:Three novel dimeric xanthones, cryptosporioptides A–C were isolated from Cryptosporiopsis sp. 8999 and their structures elucidated. Three novel dimeric xanthones, cryptosporioptides A–C were isolated from Cryptosporiopsis sp. 8999 and their structures elucidated. Methylation of cryptosporioptide A gave a methyl ester with identical NMR data to cryptosporioptide, a compound previously reported to have been isolated from the same fungus. However, HRMS analysis revealed that cryptosporioptide is a symmetrical dimer, not a monomer as previously proposed, and the revised structure was elucidated by extensive NMR analysis. The genome of Cryptosporiopsis sp. 8999 was sequenced and the dimeric xanthone ( dmx ) biosynthetic gene cluster responsible for the production of the cryptosporioptides was identified. Gene disruption experiments identified a gene ( dmxR5 ) encoding a cytochrome P450 oxygenase as being responsible for the dimerisation step late in the biosynthetic pathway. Disruption of dmxR5 led to the isolation of novel monomeric xanthones. Cryptosporioptide B and C feature an unusual ethylmalonate subunit: a hrPKS and acyl CoA carboxylase are responsible for its formation. Bioinformatic analysis of the genomes of several fungi producing related xanthones, e.g. the widely occurring ergochromes, and related metabolites allows detailed annotation of the biosynthetic genes, and a rational overall biosynthetic scheme for the production of fungal dimeric xanthones to be proposed.
ISSN:2041-6520
2041-6539
DOI:10.1039/c8sc05126g