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1.
Fitoterapia ; 156: 105070, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34718093

ABSTRACT

Kiwi (Actinidia chinensis) plants are severely destroyed by canker disease which is caused by the bacterium Pseudomonas syringae pv. actinidiae (Psa). This program tries to find anti-Psa agents among secondary metabolites of endophytic fungi from kiwi plant itself. The chemical investigation on one kiwi endophytic fungi, Fusarium tricinctum, resulted in the isolation of nine new imidazole alkaloids, fusaritricines A-I (1-9) together with seven known analogues (10-16). The structures of new compounds were established by extensive spectroscopic methods. Compounds 2, 3, 9, and 13 showed good antibacterial activity against Psa with MIC values between 25 and 50 µg/mL. It is suggested that imidazole alkaloids should be potential anti-Psa agents.


Subject(s)
Actinidia/microbiology , Alkaloids/pharmacology , Anti-Bacterial Agents/pharmacology , Fusarium/chemistry , Imidazoles/pharmacology , Pseudomonas syringae/drug effects , Alkaloids/chemistry , Alkaloids/isolation & purification , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/isolation & purification , Fourier Analysis , Fruit/microbiology , Imidazoles/chemistry , Imidazoles/isolation & purification , Magnetic Resonance Imaging , Magnetic Resonance Spectroscopy , Pseudomonas syringae/isolation & purification , Spectrophotometry, Infrared , Spectrophotometry, Ultraviolet
2.
Phytochemistry ; 168: 112116, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31513947

ABSTRACT

Endophytic fungi are microorganisms located in the inter- or intracellular compartments of plant tissues but with no harmful effects. They are considered a potential source of biological compounds. The present study was conducted to investigate the molecular identification of endophytic fungi isolated from the roots of Lithospermum officinale and their potential production of shikonin. Phylogenetic analysis was performed based on the Internal Transcribed Spacer (ITS) region and the isolates were classified into five genera as follows: Alternaria, Chaetosphaeronema, Fusarium, Mucor, and Trichoderma. The study on the methanol extracts of endophytic fungi indicated that total polyphenol content had a positive relationship with antioxidant activities and the highest antioxidant activity belonged to the methanol extracts of Fusarium tricinctum and Alternaria altenata. Then, to investigate the ability of the fungal isolates to produce shikonin, a naphthoquinone compound with high biological activity, the extracts were subjected to HPLC. The results obtained from HPLC-mass spectrometry showed that shikonin could be produced only by F. tricinctum. Thus, F. tricinctum isolated from the roots of L. officinale can be presented as a new source of shikonin.


Subject(s)
Antioxidants/isolation & purification , Endophytes/chemistry , Lithospermum/microbiology , Naphthoquinones/isolation & purification , Naphthoquinones/pharmacology , Phytochemicals/isolation & purification , Antioxidants/chemistry , Antioxidants/pharmacology , Biphenyl Compounds/antagonists & inhibitors , Drug Evaluation, Preclinical , Naphthoquinones/chemistry , Phylogeny , Phytochemicals/chemistry , Phytochemicals/pharmacology , Picrates/antagonists & inhibitors , Plant Roots/microbiology
3.
Nat Prod Bioprospect ; 8(5): 391-396, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29915912

ABSTRACT

Panax notoginseng (Araliaceae) is a famous traditional Chinese medicine mainly cultivated in Yunnan and Guangxi provinces of China. Two new alkaloids, rigidiusculamide E (1) and [-(α-oxyisohexanoyl-N-methyl-leucyl)2-] (2), together with two known ones, (-)-oxysporidinone (3) and (-)-4,6'-anhydrooxysporidinone (4) were isolated from the mycelia culture of Fusarium tricinctum SYPF 7082, an endophytic fungus obtained from the healthy root of P. notoginseng. Their structures were determined on the basis of extensive spectroscopic analyses. Compounds 1-4 were tested for their inhibitory effects against NO production on Murine macrophage cell line, and the new compound 2 showed significant inhibitory activity on NO production with the IC50 value of 18.10 ± 0.16 µM.

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