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Azaphilones are a family of fungal polyketide metabolites with diverse chemical structures and biological activities with a highly oxygenated pyranoquinone bicyclic core. Here, a class of azaphilones possessing a 6/6/6/6 tetracyclic ring system was identified in Aspergillus terreus, and exhibited potential anticancer activities. The gene deletions and biochemical investigations demonstrated that these azaphilones were collaboratively synthesized by two separate clusters containing four core-enzymes, two nonreducing PKSs, one highly reducing PKS, and one NRPS-like. More interestingly, we found that the biosynthesis is coordinately regulated by a crosstalk mechanism between these two gene clusters based on three transcriptional factors. This is a meaningful mechanism of fungal secondary metabolism, which allows fungi to synthesize more complex compounds and gain new physiological functions. The results provide a new insight into fungal natural product biosynthesis.
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Huang et al. (Tue,) studied this question.
synapsesocial.com/papers/69d95d2c5e5bcb4e3b835c66 — DOI: https://doi.org/10.1002/anie.201915514
Xuenian Huang
Chinese Academy of Sciences
Wei Zhang
Nanjing University of Science and Technology
Shen Tang
Helmholtz Institute for Pharmaceutical Research Saarland
Angewandte Chemie International Edition
Chinese Academy of Sciences
Qingdao Institute of Bioenergy and Bioprocess Technology
Qingdao National Laboratory for Marine Science and Technology
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