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1.
Eur J Mass Spectrom (Chichester) ; 26(4): 281-291, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32362135

ABSTRACT

Fungi are an important source of natural products found in a variety of plant species. A wide range of methods for the detection of metabolites present in fungi have been reported in the literature. The search for methodologies that allow the rapid detection of compounds present in crude extracts is crucial to enable the metabolite annotation doing a qualitative analysis of the complex matrix. Mass spectrometry is an important ally when it comes to in silico detection of previously reported metabolites. In this work, the ethyl acetate extract of Fusarium solani was analyzed by gas chromatography coupled to mass spectrometry (GC/MS) after derivatization process. The ethyl acetate extract was also investigated by liquid chromatography coupled with high-resolution tandem mass spectrometry assisted by the UNIFI software system. A library containing previously reported metabolites from the Fusarium genus was added to the UNIFI platform. Simultaneously, the extract was analyzed through anticholinesterase and antifungal assays. The analysis of the derivatized extract by GC/MS led to the putative identification of five metabolites, and the investigation using Ultra-High Performance Liquid Chromatography - Quadrupole Time-of-Flight Mass Spectrometry (UPLC-QTOF) analysis in data-independent acquisition mode (mass spectrometry) led to the annotation of 15 compounds present in the built-in Fusarium library added to the UNIFI system. The Fusarium solani extract showed potential anticholinesterase and in vitro antifungal activity supported by the detection of bioactive metabolites.


Subject(s)
Chromatography, High Pressure Liquid/methods , Fusarium/chemistry , Fusarium/metabolism , Gas Chromatography-Mass Spectrometry/methods , Metabolomics/methods , Senna Plant/microbiology , Software , Information Systems
2.
Biol Pharm Bull ; 42(9): 1581-1589, 2019.
Article in English | MEDLINE | ID: mdl-31474718

ABSTRACT

As a bacterium used in industry for production of several amino acids, an endotoxin-free Corynebacterium (C.) glutamicum is well known. However, it is also true that the endotoxin-producing other Corynebacterium species is present. An aim of this study is to obtain a lactic acid bacterium (LAB) that produces ornithine and citrulline at high levels. We successfully isolated a strain, designated K-28, and identified it as Weissella (W.) confusa. The production of ornithine and citrulline by K-28 was 18 ± 1 and 10 ± 2 g/L, respectively, with a 100 ± 9% conversion rate when arginine was continuously fed into a jar fermenter. Although the ornithine high production using C. glutamicum is industrially present, the strains have been genetically modified. In that connection, the wild-type of C. glutamicum produces only 0.5 g/L ornithine, indicating that W. confusa K-28 is superior to C. glutamicum to use a probiotic microorganism. We confirmed that W. confusa K-28 harbors an arginine deiminase (ADI) gene cluster, wkaABDCR. The production of ornithine and the expression of these genes significantly decreased under the aerobic condition rather than anaerobic one. The expression level of the five genes did not differ with or without arginine, suggesting that the production of amino acids in the K-28 strain was not induced by exogenous arginine.


Subject(s)
Citrulline/biosynthesis , Flowers/microbiology , Ornithine/biosynthesis , Senna Plant/microbiology , Weissella/metabolism , Animals , Citrulline/toxicity , Male , Ornithine/toxicity , Probiotics , Rats, Sprague-Dawley , Rats, Wistar , Toxicity Tests, Acute , Weissella/isolation & purification
3.
Molecules ; 19(5): 6597-608, 2014 May 22.
Article in English | MEDLINE | ID: mdl-24858094

ABSTRACT

Chemical investigation of an acetonitrile fraction from the endophytic fungus Phomopsis sp. led to the isolation of the new natural product 2-hydroxy-alternariol (7) together with the known compounds cytochalasins J (1) and H (2), 5'-epialtenuene (3) and the mycotoxins alternariol monomethyl ether (AME, 4), alternariol (AOH, 5) and cytosporone C (6). The structure of the new compound was elucidated by using 1-D and 2-D NMR (nuclear magnetic resonance) and high resolution mass spectrometry. The cytochalasins J (1) and H (2) and AOH (5) exhibited potent inhibition of the total ROS (reactive oxygen species) produced by stimulated human neutrophils and acted as potent potential anti-inflammatory agents. Moreover, cytochalasin H (2) demonstrated antifungal and acetylcholinesterase enzyme (AChE) inhibition in vitro.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Antifungal Agents/pharmacology , Ascomycota/metabolism , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Antifungal Agents/chemistry , Antioxidants/chemistry , Antioxidants/pharmacology , Ascomycota/chemistry , Cholinesterase Inhibitors/chemistry , Cholinesterase Inhibitors/pharmacology , Cytochalasins/chemistry , Cytochalasins/pharmacology , Drug Evaluation, Preclinical/methods , Endophytes/metabolism , Humans , Lactones , Magnetic Resonance Spectroscopy , Molecular Structure , Mycotoxins/chemistry , Mycotoxins/metabolism , Neutrophils/drug effects , Neutrophils/metabolism , Reactive Oxygen Species/metabolism , Secondary Metabolism , Senna Plant/microbiology , Sesquiterpenes/chemistry , Sesquiterpenes/pharmacology
4.
World J Microbiol Biotechnol ; 28(9): 2849-57, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22806725

ABSTRACT

Plant growth promoting rhizobacteria (PGPR) are an attractive eco-friendly alternative to chemicals in agriculture. While the rhizospheres of crop plants have been well studied with the objective of screening PGPR, weeds, which play an important role in maintaining ecological balance, have largely been ignored. The rhizosphere of a luxuriantly growing, medicinal weed, Cassia occidentalis was analysed by enumerating PGPR on N free media from the most diverse stage of plant (determined by profiles obtained on denaturing gradient gel electrophoresis). Each isolate was tested for other plant growth promotion assays including production of cellulase, indole acetic acid (IAA), ammonia, HCN, siderophore and chitinase to select for ones possessing multi-trait plant growth promoting (PGP) properties. Selected isolates were used for bacterization of Vigna radiata and Vigna mungo to evaluate their efficacy in promoting plant's growth in seedling germination and axenic pot conditions. Thirty five isolates were analysed further for the array of PGP properties they exhibit. A total of 6 isolates were shortlisted on the basis of maximum traits positive, amount of phosphate solubilized and IAA produced. V. radiata responded well to seed bacterization during seedling germination. A maximum increase of approximately 36 and 60 % was observed for shoot and root length, respectively in V. radiata in axenic pot culture over control plants. Extensive branching of roots was also observed with isolate NL, which produced the maximum amount of IAA. Present study investigated the plant growth promoting isolates obtained on N free media in the rhizosphere of C. occidentalis, which have the potential to be used as inoculants for other crops. This provides a new dimension to the significance of weeds in agricultural ecosystems. The study opens up possibilities for utilization of this property of weeds in plant growth promotion, and subsequent enhancement of yield for agricultural crops.


Subject(s)
Bacteria/isolation & purification , Rhizosphere , Senna Plant/growth & development , Senna Plant/microbiology , Soil Microbiology , Bacteria/classification , Chitinases/metabolism , Crops, Agricultural/growth & development , Crops, Agricultural/microbiology , Culture Media , DNA, Bacterial/genetics , Denaturing Gradient Gel Electrophoresis , Fabaceae/growth & development , Fabaceae/microbiology , Germination , Indoleacetic Acids/metabolism , Oxidoreductases/genetics , Oxidoreductases/metabolism , Phosphates/metabolism , Phylogeny , Plant Roots/growth & development , Plant Roots/microbiology , RNA, Ribosomal, 16S/genetics , Seeds/growth & development , Seeds/microbiology , Siderophores/metabolism
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