4.6 Article

Metabolic and pharmacological profiling of Penicillium claviforme by a combination of experimental and bioinformatic approaches

Journal

ANNALS OF MEDICINE
Volume 54, Issue 1, Pages 2102-2114

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/07853890.2022.2102205

Keywords

Penicillium claviforme; metabolic profiling; molecular docking; pharmacological activities

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This study presents the first complete metabolome of Penicillium claviforme, which is found to contain biologically relevant compounds. The study demonstrates that the fungus exhibits significant pharmacological activities, including antioxidant, cytotoxic, and antinociceptive effects. The findings are supported by a molecular docking study.
Background Penicillium produces a wide range of structurally diverse metabolites with significant pharmacological impacts in medicine and agriculture. For the first time, a complete metabolome of Penicillium claviforme (P. claviforme) (FBP-DNA-1205) was studied alongside pharmacological research in this study. Methods The metabolic profile of P. claviforme fermented on Potato Dextrose Broth (PDB) was investigated in this work. The complete metabolomics studies of fungus were performed using GC-MS and LC-MS-QTOF techniques. An in vitro model was utilised to study the cytotoxic and antioxidant activities, while an in vivo model was employed to investigate the antinociceptive and acute toxicity activities. Molecular Operating Environment (MOE) software was used for molecular docking analysis. Results GC-MS study showed the presence of alkanes, fatty acids, esters, azo and alcoholic compounds. Maculosin, obtain, phalluside, quinoline, 4,4'-diaminostilbene, funaltrexamine, amobarbital, and fraxetin were among the secondary metabolites identified using the LC-MS-QTOF technique. The n-hexane fraction of P. claviforme displayed significant cytotoxic activity in vitro, with an LD50 value of 92.22 mu gml(-1). The antinociceptive effects in vivo were dose-dependent significantly (p < .001). Interestingly, during the 72 h of investigation, no acute toxicity was demonstrated. In addition, a docking study of tentatively identified metabolites against the inflammatory enzyme (COX-2) supported the antinociceptive effect in an in silico model. Conclusion Metabolic profile of P. claviforme shows the presence of biologically relevant compounds in ethyl acetate extract. In addition, P. claviforme exhibits substantial antioxidant and cytotoxic activities in an in vitro model as well as antinociceptive activity in an in vivo model. The antinociceptive action is also supported by a molecular docking study. This research has opened up new possibilities in the disciplines of mycology, agriculture, and pharmaceutics. Key messages The first time explored complete metabolome through GC-MS and LC-MS-QTOF. Both in vivo & in vitro pharmacological investigation of P. claviforme. In silico molecular docking of LC-MS-QTOF metabolites.

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