Bioprocess Development Department, Genetic Engineering and Biotechnology Research Institute (GEBRI), City of Scientific Research and Technological Applications (SRTA City), New Borg El-Arab City, Alexandria, 21934, Egypt.
Nanoscience Laboratory for Environmental and Biomedical Applications (NLEBA), Semiconductor Lab., Department of Physics, Faculty of Education, Ain Shams University, Roxy, Cairo, 11757, Egypt.
Sci Rep. 2023 Feb 4;13(1):2052. doi: 10.1038/s41598-023-28749-z.
This report provides the first description of the myco-synthesis of rod-shaped MnO NPs with an average crystallite size of ~ 35 nm, employing extracellular bioactive metabolites of endophytic Trichoderma virens strain EG92 as capping/reducing agents and MnCl·4HO as a parent component. The wheat bran medium was chosen to grow endophytic strain EG92, which produced a variety of bioactive metabolites in extracellular fraction, which increases the yield of MnO NPs to 9.53 g/l. The whole medium and fungal growth conditions that influenced biomass generation were optimized as successive statistical optimization approaches (Plackett-Burman and Box-Behnken designs). The production improvements were achieved at pH 5.5, WBE (35%), and inoculum size (10%), which increased X to twelve-folds (89.63 g/l); thereby, P increased to eight-folds (82.93 g/l). After 162 h, X (145.63 g/l) and P (99.52 g/l) on the side of µ and Y were determined as 0.084 and 7.65, respectively. Via Taguchi experimental design, fungus-fabricated MnO NPs reaction was improved by adding 0.25 M of MnCl·4HO to 100% of fungal extract (reducing/capping agents) and adjusting the reaction pH adjusted to ~ 5. This reaction was incubated at 60 °C for 5 h before adding 20% fungal extract (stabilizing agent). Also, P was raised 40-fold (395.36 g/l) over the BC. Our myco-synthesized MnO NPs exhibit faster and more precise antagonistic actions against phytopathogenic bacteria than fungi; they could be employed as an alternative and promised nano-bio-pesticide to manage a variety of different types of disease-pathogens in the future.
本报告首次描述了利用内生真菌 Trichoderma virens 菌株 EG92 的细胞外生物活性代谢产物作为包覆/还原试剂,以 MnCl·4HO 为母体成分,合成棒状 MnO NPs 的方法。选择麦麸培养基来培养内生菌株 EG92,该菌株在细胞外部分产生多种生物活性代谢产物,从而将 MnO NPs 的产量提高到 9.53 g/L。采用 Plackett-Burman 和 Box-Behnken 设计等连续统计优化方法优化整个培养基和真菌生长条件,以提高生物量的生成。在 pH 5.5、WBE(35%)和接种量(10%)下,实现了生产的提高,使 X 增加到 12 倍(89.63 g/L);因此,P 增加到 8 倍(82.93 g/L)。162 小时后,在 µ 的侧面,X(145.63 g/L)和 P(99.52 g/L)分别确定为 0.084 和 7.65。通过 Taguchi 实验设计,通过向 100%真菌提取物(还原/包覆试剂)中添加 0.25 M 的 MnCl·4HO 并将反应 pH 调节至~5,改进了真菌制备的 MnO NPs 反应。该反应在 60°C 下孵育 5 小时后,再加入 20%的真菌提取物(稳定剂)。此外,P 比 BC 提高了 40 倍(395.36 g/L)。我们的真菌合成的 MnO NPs 对植物病原菌的拮抗作用比真菌更快、更精确;它们将来可以作为一种替代和有前途的纳米生物农药,用于防治各种不同类型的疾病病原体。