Evidence map›Paper›PMID 42715223›Full record

ArticlePloS one2026

UPLC-MS metabolite profiling and antioxidant efficacy of Neopestalotiopsisclavispora isolated from Oroxylum indicum (L.) Kurz Stem Bark.

Sushma Swaroopa, Amshumala Bhoothakallu Lolajaksha, Tamizh Selvan Gnanasekaran, Pavan Gollapalli, Vishakh Radhakrishna Kedilaya, Sharmila Kameyanda Poonacha

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sushma SwaroopaNitte (Deemed to be University), KS Hegde Medical Academy (KSHEMA), Central Research Laboratory, Mangaluru, Karnataka, India.
Amshumala Bhoothakallu LolajakshaNitte (Deemed to be University), KS Hegde Medical Academy (KSHEMA), Central Research Laboratory, Mangaluru, Karnataka, India.
Tamizh Selvan GnanasekaranNitte (Deemed to be University), KS Hegde Medical Academy (KSHEMA), Central Research Laboratory, Mangaluru, Karnataka, India.
Pavan GollapalliDepartment of Bioinformatics and Biostatistics, Nitte (Deemed to be University), Nitte University Centre for Science Education and Research (NUCSER), Paneer Campus, Mangaluru, Karnataka, India.
Vishakh Radhakrishna KedilayaNitte (Deemed to be University), KS Hegde Medical Academy (KSHEMA), Central Research Laboratory, Mangaluru, Karnataka, India.
Sharmila Kameyanda PoonachaNitte (Deemed to be University), KS Hegde Medical Academy (KSHEMA), Central Research Laboratory, Mangaluru, Karnataka, India.ORCID https://orcid.org/0000-0002-1604-2120

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endophytic fungi represent a valuable source of bioactive compounds with diverse pharmacological properties. In this study, we explored the antioxidant potential of secondary metabolites produced by Neopestalotiopsis clavispora (N.clavispora), an endophytic fungus isolated from Oroxylum indicum Kurz stem bark. N.clavispora extract was subjected to UPLC-MS analysis to profile its bioactive components, and its antioxidant capacity was assessed using the DPPH (1,1-diphenyl-2-picrylhydrazyl) free radical scavenging assay. For in vivo evaluation, Swiss albino mice were administered with 100 mg/kg bodyweight dose of extract for five consecutive days, followed by exposure to 2 Gy of gamma radiation at a dose rate of 3.58 Gy/min. Subsequent measurements of superoxide dismutase (SOD) activity in liver homogenate were conducted to assess antioxidant enzyme response. The data obtained from UPLC-MS, showed, cimicifoetiside B (identified by UNIFI database matching; 44% relative abundance) as the predominant metabolite. N. clavispora extract showed moderate DPPH scavenging (IC₅₀ 82.86 μg/mL vs ascorbic acid 19.01 μg/mL). Molecular docking using cimicifoetiside B against the antioxidant enzyme Superoxide dismutase (SOD), revealing a docking score of -4.96 kcal/mol with 1 hydrogen bond. Molecular dynamics simulations confirmed the interaction with a binding energy of -12.36 ± 02.32 kcal/mol. Binding affinities and molecular interaction profiles indicated possible association with SOD. In vivo, N.clavispora extract at 100 mg/kg body weight/day yielded SOD activity of 1.98 ± 0.38 vs. radiation group 0.78 ± 0.13. These results suggest N.clavispora may have antioxidant related activity under the conditions tested, supporting further in vitro and in vivo studies.

Indexed as

AntioxidantsAscomycotaBignoniaceaePlant BarkAnimalsBiphenyl CompoundsChromatography, High Pressure LiquidLiverMass SpectrometryMiceMolecular Docking SimulationSuperoxide DismutaseAntioxidantsBiphenyl CompoundsSuperoxide Dismutase

Identifiers

PMID42715223
PMCPMC13557386

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