4.7 Article

Ophiobolin Sesterterpenoids and Farnesylated Phthalide Derivatives from the Deep Sea Cold-Seep-Derived Fungus Aspergillus insuetus SD-512

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 83, Issue 12, Pages 3652-3660

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.0c00860

Keywords

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Funding

  1. National Key R&D Program of China [2018YFC0310800]
  2. National Natural Science Foundation of China [42076090, U2006203]
  3. Shandong Provincial Natural Science Foundation [ZR2019ZD18]
  4. Basic Applied Research program of Qingdao [19-6-2-40-cg]
  5. Research Vessel KEXUE of the National Major Science and Technology Infrastructure from the Chinese Academy of Sciences [KEXUE2018G28]
  6. Taishan Scholar Project from Shandong Province [ts201511060]

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Three new ophiobolin sesterterpenoids, (6R)-16,17,21,21-O-tetrahydroophiobolin G (1), (6R)-16,17-dihydroophiobolin H (2), and (5S,6S)-16,17-dihydroophiobolin H (3), and three new farnesylated phthalide derivatives farnesylemefuranones D-F ( 9-11), along with five known ophiobolin analogues (4-8), were isolated and identified from the culture extract of Aspergillus insuetus SD-512, a deep-sea-derived fungus obtained from cold seep sediments collected at a depth of 1331 m. Among them, compounds 9-11 are rare examples of phthalide derivatives linked with farnesyl moieties via ether bonds. Their structures were established on the basis of detailed interpretation of the NMR spectroscopic and mass spectrometric data. X-ray crystallographic analysis, ECD calculations, and DP4+ probability analysis were performed to confirm the structures and establish the relative and absolute configurations of compounds 1-4. Compounds 3 and 9-11 showed broad-spectrum antibacterial activities, and differences in potencies could be assigned to structural modifications. This is the first report of secondary metabolites obtained from a deep sea cold-seep-derived fungus.

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