Efficient identification of fungal antimicrobial principles by tandem MS and NMR database

被引:9
作者
Lee, Ming-Shian [1 ]
Yang, Yu-Liang [2 ]
Wu, Chia-Yen [3 ]
Chen, Ying-Lien [3 ]
Lee, Ching-Kuo [4 ]
Tzean, Shean-Shong [3 ]
Lee, Tzong-Huei [5 ]
机构
[1] Taipei Med Univ, Sch Pharm, Taipei, Taiwan
[2] Acad Sinica, Agr Biotechnol Res Ctr, Taipei, Taiwan
[3] Natl Taiwan Univ, Dept Plant Pathol & Microbiol, Taipei, Taiwan
[4] Taipei Med Univ, Grad Inst Pharmacognosy, Taipei, Taiwan
[5] Natl Taiwan Univ, Inst Fisheries Sci, Taipei, Taiwan
关键词
Phoma herbarum; Cryptosporiopsis ericae; Albifimbria verrucaria; Molecular networking; Dereplication; NATURAL-PRODUCTS; DEREPLICATION; METABOLITES;
D O I
10.1016/j.jfda.2019.06.003
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The continuous re-isolation of the known and non-applicable compounds that is time-consuming and wasting resources is still a critical problem in the discovery of bioactive entities from natural resources. To efficiently address the problem, high performance liquid chromatography-diode array detector-microfractionation (HPLC-DAD-microfractionation) guided by disk agar diffusion assay was developed, and the active compounds were further identified using the tandem mass spectrometry (MS/MS)-based molecular networking. Of 150 fungal strains screened, the methanolic extracts of Phoma herbarum PPM7487, Cryptosporiopsis ericae PPM7405, and Albifinibria verrucaria PPM945 exhibited potent antimicrobial activity against Candida albicans SC5314 and Cryptococcus neoformans H99 in the preliminary agar diffusion assay. The concept of OSMAC (one strain many compounds) was employed in the fungal cultures in order to enrich the diversity of the 2 nd metabolites in this study. HPLC coupled with off-line bioactivity-directed profiling of the extracts enabled a precise localization of the compounds responsible for the conspicuous antimicrobial activity. The purified active compounds were identified based mainly on MS/MS database, and further supported by C-13 nuclear magnetic resonance (NMR) spectral data compared to the literatures. In addition to nineteen known compounds, a new trichothecene derivative 1, namely trichoverrin D, was isolated and identified through this protocol. The antifungal activities of all the pure isolates were evaluated, and the structure activity relationships were also inferred. This report has demonstrated the combination of HPLC microfractination and MS/MS coupled by NMR spectral dereplication for speeding up the antimicrobial natural products discovery process. Copyright (C) 2019, Food and Drug Administration, Taiwan. Published by Elsevier Taiwan LLC.
引用
收藏
页码:860 / 868
页数:9
相关论文
共 18 条
[1]  
Bérdy J, 2012, J ANTIBIOT, V65, P385, DOI [10.1038/ja.2012.27, 10.1038/ja.2012.54]
[2]   Natural products: A continuing source of novel drug leads [J].
Cragg, Gordon M. ;
Newman, David J. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2013, 1830 (06) :3670-3695
[3]   Microbial drug discovery: 80 years of progress [J].
Demain, Arnold L. ;
Sanchez, Sergio .
JOURNAL OF ANTIBIOTICS, 2009, 62 (01) :5-16
[4]   High-Resolution MS, MS/MS, and UV Database of Fungal Secondary Metabolites as a Dereplication Protocol for Bioactive Natural Products [J].
El-Elimat, Tamam ;
Figueroa, Mario ;
Ehrmann, Brandie M. ;
Cech, Nadja B. ;
Pearce, Cedric J. ;
Oberlies, Nicholas H. .
JOURNAL OF NATURAL PRODUCTS, 2013, 76 (09) :1709-1716
[5]   Approaches to automating the dereplication of bioactive natural products - The key step in high throughput screening of bioactive materials from natural sources [J].
Hook, DJ ;
Pack, EJ ;
Yacobucci, JJ ;
Guss, J .
JOURNAL OF BIOMOLECULAR SCREENING, 1997, 2 (03) :145-152
[6]   INTEGRATED BIOLOGICAL PHYSICOCHEMICAL SYSTEM FOR THE IDENTIFICATION OF ANTITUMOR COMPOUNDS IN FERMENTATION BROTHS [J].
HOOK, DJ ;
MORE, CF ;
YACOBUCCI, JJ ;
DUBAY, G ;
OCONNOR, S .
JOURNAL OF CHROMATOGRAPHY, 1987, 385 :99-108
[7]   Dereplication of microbial extracts and related analytical technologies [J].
Ito, Tatsuya ;
Masubuchi, Miyako .
JOURNAL OF ANTIBIOTICS, 2014, 67 (05) :353-360
[8]   12,13-DEOXYTRICHOVERRINS FROM MYROTHECIUM-VERRUCARIA [J].
JARVIS, BB ;
MIDIWO, JO ;
GUO, MD .
JOURNAL OF NATURAL PRODUCTS, 1989, 52 (03) :663-665
[9]   NEW TRICHOVERROIDS FROM MYROTHECIUM-VERRUCARIA ISOLATED BY HIGH-SPEED COUNTERCURRENT CHROMATOGRAPHY [J].
JARVIS, BB ;
DESILVA, T ;
MCALPINE, JB ;
SWANSON, SJ ;
WHITTERN, DN .
JOURNAL OF NATURAL PRODUCTS, 1992, 55 (10) :1441-1446
[10]   Combining Mass Spectrometric Metabolic Profiling with Genomic Analysis: A Powerful Approach for Discovering Natural Products from Cyanobacteria [J].
Kleigrewe, Karin ;
Almaliti, Jehad ;
Tian, Isaac Yuheng ;
Kinnel, Robin B. ;
Korobeynikov, Anton ;
Monroe, Emily A. ;
Duggan, Brendan M. ;
Di Marzo, Vincenzo ;
Sherman, David H. ;
Dorrestein, Pieter C. ;
Gerwick, Lena ;
Gerwick, William H. .
JOURNAL OF NATURAL PRODUCTS, 2015, 78 (07) :1671-1682