From Bench to Greenhouse: The Comparative Nano-Bio System Effects of Green-Synthesized TiO(2)-NPs and Plant-Growth-Promoting Microorganisms in Capsicum annuum

从实验室到温室:绿色合成的二氧化钛纳米颗粒和植物促生微生物对辣椒的纳米生物系统效应比较研究

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Abstract

In this study, titanium dioxide nanoparticles (TiO(2)-NPs) were produced via green routes using blueberry extracts obtained with isopropanol (I-TiO(2)-NPs) and methanol (M-TiO(2) NPs). HPLC-DAD confirmed phenolic/flavonoid profiles in the extracts, and spectroscopy/microscopy established anatase, polyhedral, mesoporous TiO(2)-NPs with Eg ≈ 3.0 eV, hydrodynamic sizes ≈ 130-150 nm and negative ζ-potentials (-33 to -50 mV). The in vitro compatibility between TiO(2)-NPs and the plant-growth-promoting microorganisms (PGPMs) Bacillus subtilis (Bs), Bacillus thuringiensis (B), and Trichoderma harzianum (T) sustained increased growth up to 150 µg/mL without visible negative effects. In greenhouse experimentation of Capsicum annuum exposed to low-moderate TiO(2)-NPs, an increased leaf number and plant height were observed, while root length did not exceed the controls. I-TiO(2) at moderate concentrations, particularly with a single PGPM (B or T), promoted fresh and dry biomass accumulation. Biochemically, peroxidase rose sharply for M-TiO(2) at a low dose with consortium, whereas I-TiO(2) elicited broader antioxidant responses; total protein increased at higher doses for both formulations, and total chlorophyll was highest with I-TiO(2) (high dose with or without PGPMS). Collectively, the nano-bio system shows a formulation- and dose-dependent biphasic behavior: (I) I-TiO(2) enhances biomass and photosynthetic pigments; (II) M-TiO(2) favors strong POX induction under specific microorganism-dose combinations; and (III) single PGPM co-application with I-TiO(2)-NPs or M-TiO(2) NPs outperforms consortia under our experimental conditions. Green synthesis thus provides surface functionalities that improve dispersion, microbial compatibility, and predictable physiological/biochemical outcomes for precision agriculture.

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