Identification of the decumbenone biosynthetic gene cluster in penicillium decumbens and the importance for production of calbistrin
Artikel i vetenskaplig tidskrift, 2018

Background:
Filamentous fungi are important producers of secondary metabolites, low molecular weight molecules that often have bioactive properties. Calbistrin A is a secondary metabolite with an interesting structure that was recently found to have bioactivity against leukemia cells. It consists of two polyketides linked by an ester bond: a bicy-clic decalin containing polyketide with structural similarities to lovastatin, and a linear 12 carbon dioic acid structure. Calbistrin A is known to be produced by several uniseriate black Aspergilli, Aspergillus versicolor-related species, and Penicillia. Penicillium decumbens produces calbistrin A and B as well as several putative intermediates of the calbistrin pathway, such as decumbenone A-B and versiol.
Results:
A comparative genomics study focused on the polyketide synthase (PKS) sets found in three full genome sequence calbistrin producing fungal species, P. decumbens, A. aculeatus and A. versicolor, resulted in the identification of a novel, putative 13-membered calbistrin producing gene cluster (calA to calM). Implementation of the CRISPR/ Cas9 technology in P. decumbens allowed the targeted deletion of genes encoding a polyketide synthase (calA), a major facilitator pump (calB) and a binuclear zinc cluster transcription factor (calC). Detailed metabolic profiling, using UHPLC-MS, of the ∆calA (PKS) and ∆calC ( TF) strains confirmed the suspected involvement in calbistrin productions as neither strains produced calbistrin nor any of the putative intermediates in the pathway. Similarly analysis of the excreted metabolites in the ∆calB (MFC-pump) strain showed that the encoded pump was required for efficient export of calbistrin A and B.
Conclusion:
Here we report the discovery of a gene cluster (calA-M) involved in the biosynthesis of the polyketide calbistrin in P. decumbens. Targeted gene deletions proved the involvement of CalA (polyketide synthase) in the biosynthesis of calbistrin, CalB (major facilitator pump) for the export of calbistrin A and B and CalC for the transcriptional regulation of the cal-cluster. This study lays the foundation for further characterization of the calbistrin biosynthetic pathway in multiple species and the development of an efficient calbistrin producing cell factory.

Biosynthesis

Polyketide

Decalin

Secondary metabolite

Calbistrin

Penicillium decumbens

Författare

S. Grijseels

Danmarks Tekniske Universitet (DTU)

Carsten Pohl

Rijksuniversiteit Groningen

Jens Christian Froslev Nielsen

Chalmers, Biologi och bioteknik, Systembiologi

Novo Nordisk Foundation Center for Biosustainability

Zahida Wasil

Danmarks Tekniske Universitet (DTU)

Yvonne Nygård

Rijksuniversiteit Groningen

Jens B Nielsen

Chalmers, Biologi och bioteknik, Systembiologi

Danmarks Tekniske Universitet (DTU)

J. C. Frisvad

Danmarks Tekniske Universitet (DTU)

K. F. Nielsen

Danmarks Tekniske Universitet (DTU)

M. Workman

Danmarks Tekniske Universitet (DTU)

Thomas Ostenfeld Larsen

Danmarks Tekniske Universitet (DTU)

Arnold J.M. Driessen

Rijksuniversiteit Groningen

Rasmus John Normand Frandsen

Danmarks Tekniske Universitet (DTU)

Fungal Biology and Biotechnology

20543085 (eISSN)

Vol. 5 1 1-17 18

Ämneskategorier

Mikrobiologi

Bioinformatik och systembiologi

Genetik

DOI

10.1186/s40694-018-0063-4

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Senast uppdaterat

2021-01-22