Antibacterial and antifungal screening of natural products sourced from Australian fungi and characterisation of pestalactams D-F

被引:17
作者
Beattie, Karren D. [1 ]
Ellwood, Nicola [1 ]
Kumar, Rohitesh [1 ]
Yang, Xinzhou [1 ]
Healy, Peter C. [2 ]
Choomuenwai, Vanida [1 ]
Quinn, Ronald J. [1 ]
Elliott, Alysha G. [3 ]
Huang, Johnny X. [3 ]
Chitty, Jessica L. [4 ]
Fraser, James A. [4 ]
Cooper, Matthew A. [3 ]
Davis, Rohan A. [1 ]
机构
[1] Griffith Univ, Eskitis Inst Drug Discovery, Brisbane, Qld 4111, Australia
[2] Griffith Univ, Sch Nat Sci, Brisbane, Qld 4111, Australia
[3] Univ Queensland, Inst Mol Biosci, St Lucia, Qld 4072, Australia
[4] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld 4072, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
Pestalotiopsis; Amphisphaeriaceae; Fungal natural products; Pestalactams A-F; Pestalactam; Caprolactam; X-ray crystal structure; Antibacterial; Antifungal; MIC screening; ENDOPHYTIC FUNGUS; PESTALOTIOPSIS-MICROSPORA; GENUS XYLARIA; A-C; METABOLITE; MICROFUNGUS; POLYKETIDES; PISTILLARIN; TAXONOMY; ACID;
D O I
10.1016/j.phytochem.2015.12.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eighteen natural products sourced from Australian micro- or macro-fungi were screened for antibacterial and antifungal activity. This focused library was comprised of caprolactams, polyamines, quinones, and polyketides, with additional large-scale isolation studies undertaken in order to resupply previously identified compounds. Chemical investigations of the re-fermented culture from the endophytic fungus Pestalotiopsis sp. yielded three caprolactam analogues, pestalactams D-F, along with larger quantities of the known metabolite pestalactam A, which was methylated using diazomethane to yield 4-O-methylpestalactam A. The chemical structures of the previously undescribed fungal metabolites were determined by analysis of 1D/2D NMR and MS data. The structure of 4-O-methylpestalactam A was confirmed following single crystal X-ray diffraction analysis. The antibacterial and antifungal activity of all compounds was assessed, which identified three compounds, (1S,3R)-austrocortirubin, (1S,3S)austrocortirubin, and 1-deoxyaustrocortirubin with mild activity (100 mu M) against Gram-positive isolates and one compound, 2-hydroxy-6-methyt-8-methoxy-9-oxo-9H-xanthene-1-carboxylic acid, with activity against Cryptococcus neoformans and Cryptococcus gattii at 50 mu M. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:79 / 85
页数:7
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