1. Academic Validation
  2. Bioactive Chaetoglobosins from the Mangrove Endophytic Fungus Penicillium chrysogenum

Bioactive Chaetoglobosins from the Mangrove Endophytic Fungus Penicillium chrysogenum

  • Mar Drugs. 2016 Sep 27;14(10):172. doi: 10.3390/md14100172.
Song Huang 1 Haiyan Chen 2 Wensheng Li 3 Xinwei Zhu 4 Weijia Ding 5 Chunyuan Li 6
Affiliations

Affiliations

  • 1 College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China. singsongpine@sina.cn.
  • 2 School of Chemistry and Chemical Engineering, Guangxi University, Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development, Nanning 530004, China. czyzsu@gxu.edu.cn.
  • 3 College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China. wsliscau@sina.com.
  • 4 College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China. zhuxw2580@sina.com.
  • 5 College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China. dwjzsu@scau.edu.cn.
  • 6 College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China. chunyuanli@scau.edu.cn.
Abstract

A novel chaetoglobosin named penochalasin I (1) with a unprecedented six-cyclic 6/5/6/5/6/13 fused ring system, and another new chaetoglobosin named penochalasin J (2), along with chaetoglobosins G, F, C, A, E, armochaetoglobosin I, and cytoglobosin C (3-9) were isolated from the culture of Penicillium chrysogenum V11. Their structures were elucidated by 1D, 2D NMR spectroscopic analysis and high resolution mass spectroscopic data. The absolute configuration of compounds 1 and 2 were determined by comparing the theoretical electronic circular dichroism (ECD) calculation with the experimental CD. Compound 1 was the first example, with a six-cyclic fused ring system formed by the connection of C-5 and C-2' of the chaetoglobosin class. Compounds 5-8 remarkably inhibited the plant pathogenic fungus R. solani (minimum inhibitory concentrations (MICs) = 11.79-23.66 μM), and compounds 2, 6, and 7 greatly inhibited C. gloeosporioides (MICs = 23.58-47.35 μM), showing an Antifungal activity higher than that of carbendazim. Compound 1 exhibited marked cytotoxicity against MDA-MB-435 and SGC-7901 cells (IC50 < 10 μM), and compounds 6 and 9 showed potent cytotoxicity against SGC-7901 and A549 cells (IC50 < 10 μM).

Keywords

Penicillium chrysogenum; antifungal activity; chaetoglobosin; cytotoxicity; marine mangrove fungus.

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