Bioprospecting endophytic fungi from Fusarium genus as sources of bioactive metabolites.
Kouipou Rufin Marie ToghueoPublished in: Mycology (2019)
Endophytic fungi became an attractive source for the discovery of new leads, because of the complexity and the structural diversity of their secondary metabolites. The genus Fusarium comprising about 70 species is extremely variable in terms of genetics, biology, ecology, and consequently, secondary metabolism and have been isolated from countless plants genera from diverse habitats. These endophytic microbes may provide protection and survival strategies in their host plants with production of a repertoire of chemically diverse and structurally unprecedented secondary metabolites reported to exhibit an incredible array of biological activities including antimicrobial, anticancer, antiviral, antioxidants, antiparasitics, immunosuppressants, immunomodulatory, antithrombotic, and biocontrol ability against plants pathogens and nematodes. This review comprehensively highlights over the period 1981-2019, the bioactive potential of metabolites produced by endophytes from Fusarium genus. Abbreviations: AIDS: Acquired immune deficiency syndrome; BAPT: C-13 phenylpropanoid side chain-CoA acyltransferase; CaBr2: Calcium bromide; DBAT: 10-deacetylbaccatin III-10-O-acetyl transferase; DNA: Deoxyribonucleic acid; EI-MS: Electron ionization mass spectrometer; EN: Enniatin; ERK: Extracellular regulated protein kinase; EtOAc: Ethyl acetate; FDA: Food and Drug Administration; GAE/g: Gallic acid equivalent per gram; GC-MS: Gas chromatography-mass spectrometry; HA: Hyperactivation; HCV: Hepatitis C Virus; HCVPR: Hepatitis C Virus protease; HeLa: Human cervical cancer cell line; HIV: Human immunodeficiency viruses; HPLC: High Performance Liquid Chromatography; IAA: Indole-3-acetic acid; IARC: International Agency for Research on Cancer; IC50: Half maximal inhibitory concentration; LC50: Concentration of the compound that is lethal for 50% of exposed population; LC-MS: Liquid chromatography-mass spectrometry; MCF-7: Human breast cancer cell line; MDR: Multidrug-resistant; MDRSA: Multidrug-resistant S. aureus; MFC: Minimum fungicidal concentration; MIC: Minimum inhibitory concentration; MRSA: Multidrug-resistant S. aureus; MTCC: Microbial type culture collection; PBMCs: Peripheral blood mononuclear cells; PCR: Polymerase chain reaction; TB: Tuberculosis; TLC: Thin layer chromatography; TNF: Tumor necrosis factor; WHO: World Health Organization http://www.zoobank.org/urn:lsid:zoobank.org:pub:D0A7B2D8-5952-436D-85C8-C79EAAD1013C.
Keyphrases
- mass spectrometry
- hepatitis c virus
- multidrug resistant
- high performance liquid chromatography
- liquid chromatography
- ms ms
- gram negative
- tandem mass spectrometry
- simultaneous determination
- gas chromatography
- solid phase extraction
- endothelial cells
- human immunodeficiency virus
- gas chromatography mass spectrometry
- acinetobacter baumannii
- drug resistant
- high resolution
- high resolution mass spectrometry
- induced pluripotent stem cells
- antiretroviral therapy
- drug administration
- capillary electrophoresis
- protein kinase
- rheumatoid arthritis
- small molecule
- klebsiella pneumoniae
- staphylococcus aureus
- hiv positive
- microbial community
- emergency department
- hiv aids
- signaling pathway
- fatty acid
- hiv infected
- squamous cell
- resistance training
- multiple sclerosis
- cell cycle arrest
- squamous cell carcinoma
- men who have sex with men
- single molecule
- high throughput
- escherichia coli
- cell death
- smoking cessation