4.7 Article

Mining new meroterpenoids from the marine red alga-derived endophytic Penicillium chermesinum EN-480 by comparative transcriptome analysis

Journal

BIOORGANIC CHEMISTRY
Volume 128, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2022.106021

Keywords

Penicillium chermesinum; Comparative transcriptome analysis; Meroterpenoids; Antimicrobial activitie; Plausible biosynthesis pathway

Funding

  1. National Natural Science Foundation of China [42176115]
  2. Laboratory of Marine Biology and Biotechnology of the Qingdao National Laboratory for Marine Science and Technology [YQ2018NO08]

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The transcriptome analysis of the algal endophytic fungus Penicillium chermesinum EN-480 revealed that fermentation in modified rice solid medium could lead to the production of new meroterpenoids with different structures compared to other media. These compounds showed antimicrobial activity against human- and aqua-bacteria as well as plant-pathogenic fungi. The study also discussed the possible biosynthesis pathway of these compounds.
As the development of genetic and bioinformatic, the strategy of bottom-up, combined with genome and transcriptome techniques, was considered as an efficient and practical method to break through the limitation of traditional discovery of natural products. Generally, comparative transcriptome analysis could be useful to guide the optimization of fungal cultivation conditions in which the transcriptional level of interesting compounds is higher. The transcriptome analysis of the algal endophytic fungus Penicillium chermesinum EN-480 indicated that fermentation of this fungus in modified rice solid medium could produce some metabolites different from those cultivated in other media. Four new meroterpenoids (compounds 1-4, namely, chermesins E-H) were characterized and their structures were determined by HRESIMS and NMR spectra. The absolute configurations were confirmed by NOESY experiments, X-ray diffraction analysis, and comparison of ECD cotton effects. Antimicrobial activities against human- and aqua-bacteria as well as against plant-pathogenic fungi were assayed. The plausible biosynthesis pathway of these compounds was discussed.

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