The biosynthetic pathway for aurofusarin in Fusarium graminearum reveals a close link between the naphthoquinones and naphthopyrones

• Published in: Molecular microbiology 2006-08, Vol.61 (4), p.1069-1080
• Main Authors: Frandsen, Rasmus J. N., Nielsen, Nikoline J., Maolanon, Nicolai, Sørensen, Jens C., Olsson, Stefan, Nielsen, John, Giese, Henriette
• Format: Article
• Language: English
• Subjects: Agrobacterium; Agrobacterium tumefaciens - genetics; Biological and medical sciences; Cluster analysis; Enzymes; Fundamental and applied biological sciences. Psychology; Fungal Proteins - chemistry; Fungal Proteins - genetics; Fungal Proteins - metabolism; Fungi; Fusarium - genetics; Fusarium - metabolism; Fusarium graminearum; Genes; Genes, Fungal; Microbiology; Miscellaneous; Molecules; Mutation; Mycology; Naphthalenes - chemistry; Naphthalenes - metabolism; Naphthoquinones - chemistry; Naphthoquinones - metabolism; Transcription Factors - genetics; Transformation, Bacterial
• ISSN: 0950-382X; 1365-2958
• DOI: 10.1111/j.1365-2958.2006.05295.x

Summary Fungal polyketide biosynthesis typically involves multiple enzymatic steps and the encoding genes are often found in gene clusters. A gene cluster containing PKS12, the polyketide synthase gene responsible for the synthesis of the pigment aurofusarin, was analysed by gene replacement using Agrobacterium tumefaciens‐mediated transformation to determine the biosynthesis pathway of aurofusarin. Replacement of aurR1 with hygB shows that it encodes a positively acting transcription factor that is required for the full expression of PKS12, aurJ, aurF, gip1 and FG02329.1, which belong to the gene cluster. AurR1 and PKS12 deletion mutants are unable to produce aurofusarin and rubrofusarin. Bio‐ and chemoinformatics combined with chemical analysis of replacement mutants (ΔaurJ, ΔaurF, Δgip1, ΔaurO and ΔPKS12) indicate a five‐step enzyme catalysed pathway for the biosynthesis of aurofusarin, with rubrofusarin as an intermediate. This links the biosynthesis of naphthopyrones and naphthoquinones together. Replacement of the putative transcription factor aurR2 results in an increased level of rubrofusarin relative to aurofusarin. Gip1, a putative laccase, is proposed to be responsible for the dimerization of two oxidized rubrofusarin molecules resulting in the formation of aurofusarin.