4.7 Article

A New Dihydrochromone Dimer and Other Secondary Metabolites from Cultures of the Marine Sponge-Associated Fungi Neosartorya fennelliae KUFA 0811 and Neosartorya tsunodae KUFC 9213

Journal

MARINE DRUGS
Volume 15, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/md15120375

Keywords

Neosartorya fennelliae; Neosartorya tsunodae; Trichocomaceae; dihydrochromone dimer; paecilin E; dankasterone A; chromanol derivative; marine sponge-associated fungi; antibacterial activity

Funding

  1. FCT/MCTES-Foundation for Science and Technology
  2. European Regional Development Fund (ERDF) through the COMPETE-Programa Operacional Factores de Competitividade (POFC) programme [PTDC/MAR-BIO/4694/2014, POCI-01-0145-FEDER-016790]
  3. European Regional Development Fund (ERDF)
  4. project INNOVMAR-Innovation and Sustainability in the Management and Exploitation of Marine Resources (within Research Line NOVELMAR) [NORTE-01-0145-FEDER-000035]
  5. North Portugal Regional Operational Programme (NORTE)

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A previously unreported dihydrochromone dimer, paecilin E (1), was isolated, together with eleven known compounds: beta-sitostenone, ergosta-4,6,8 (14), 22-tetraen-3-one, cyathisterone, byssochlamic acid, dehydromevalonic acid lactone, chevalone B, aszonalenin, dankasterone A (2), helvolic acid, secalonic acid A and fellutanine A, from the culture filtrate extract of the marine sponge-associated fungus Neosartorya fennelliae KUFA 0811. Nine previously reported metabolites, including a chromanol derivative (3), (3 beta, 5 alpha, 22E), 3,5-dihydroxyergosta-7,22-dien-6-one (4), byssochlamic acid, hopan-3 beta,22-diol, chevalone C, sartorypyrone B, helvolic acid, lumichrome and the alkaloid harmane were isolated from the culture of the marine-sponge associated fungus Neosartorya tsunodae KUFC 9213. Paecilin E (1), dankasterone A (2), a chromanol derivative (3), (3 beta, 5 alpha, 22E)-3,5-dihydroxyergosta-7,22-dien-6-one (4), hopan-3 beta,22-diol (5), lumichrome (6), and harmane (7) were tested for their antibacterial activity against Gram-positive and Gram-negative reference and multidrug-resistant strains isolated from the environment. While paecilin E (1) was active against S. aureus ATCC 29213 and E. faecalis ATCC 29212, dankastetrone A (2) was only effective against E. faecalis ATCC 29212 and the multidrug-resistant VRE E. faecalis A5/102. Both compounds neither inhibit biofilm mass production in any of the strains at the concentrations tested nor exhibit synergistic association with antibiotics.

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