Authors
Soumita Roy, Abir Das, Nilakshi Chakraborty, Arup Kumar Sarkar, Ribhu Maity, Tithi Maity, Bidhan Chandra Samanta, Gourav Mondal, Pradip Bhattacharyya, Anway Ganguly, Sudipta Kumar Sil, Satish V Patil, Vishnu D Rajput, Malay Kumar Adak
Published in
World journal of microbiology & biotechnology. Volume 42. Issue 10. Sep 27, 2026. Epub Sep 27, 2026.
Abstract
This study explores the bioinorganic potential of selenium nanoparticles (SeNPs) biosynthesized by Bacillus sp. (AKS_bp1, PQ824612) in mitigating hexavalent chromium [Cr(VI)] toxicity in chickpea (Cicer arietinum L.). SeNPs were produced via microbial reduction of sodium selenite and characterized by nanoscale size (~ 100-150 nm), negative surface charge (- 20 mV), and biomolecular capping. Under controlled hydroponic Cr(VI) exposure (0-100 ppm), SeNP treatment significantly reduced Cr accumulation in plant tissues, with decreases of 24% in roots and 45% in shoots, indicating restricted translocation and improved metal homeostasis. This suggests a Se-mediated modulation of Cr mobility within the plant system. At the physiological and biochemical levels, SeNPs alleviated Cr-induced oxidative stress, as evidenced by reductions in superoxide (65%) and hydrogen peroxide (52%) levels, along with enhanced antioxidant defense and photosystem II efficiency (a 21% increase in photochemical performance). Improved chlorophyll fluorescence and stomatal regulation further indicated restoration of cellular functionality under metal stress. Importantly, SeNPs exhibited intrinsic redox activity with catecholase-like catalytic behavior (kcat = 3.11 × 106 s- 1), suggesting a potential role in electron-transfer processes relevant to oxidative stress modulation. Overall, bacteriogenic SeNPs mitigate Cr(VI) toxicity through a combination of reduced metal uptake, altered intracellular metal dynamics, and attenuation of reactive oxygen species. These findings highlight the bioinorganic functionality of SeNPs as redox-active nanomaterials influencing metal-plant interactions and oxidative stress pathways.
PMID:
42801395
Bibliographic data and abstract were imported from PubMed on 28 Sep 2026.
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