Ali Sikander, Zahra Hijab, Ahmad Muhammad Usman, Abdel-Rheem Amany A, Afzaal Muhammad, Nawaz Rab, Khatab Abbasi Bakar Bin, Irfan Ali, Bin Jardan Yousef A
Department of Microbiology, Dr. Ikram-Ul-Haq Institute of Industrial Biotechnology, GC University Lahore, Lahore, 54000, Pakistan.
Department of Pharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, Sohag University, Sohag, 82524, Egypt.
Microb Cell Fact. 2025 Jun 3;24(1):129. doi: 10.1186/s12934-025-02750-9.
This study reports the synthesis of hyaluronic acid-coated silver oxide (AgO) nano-adsorbents using Bacillus subtilis PV154141.1 for dual environmental and biomedical applications. Multiple parameters were optimized for the formation and constancy of HA-AgO nano-adsorbents, including silver nitrate (AgNO) concentration and reaction time. Several characterization techniques including X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), and energy dispersive X-ray (EDX) spectroscopy were employed to determine the structural properties, morphology, and elemental composition of the synthesized HA-AgO nano-adsorbents. XRD pattern confirmed the presence of AgO nano-adsorbents by showing peaks having hkl values of 110, 111, 200, 220, 311, and 222, located at 2θ values of roughly 26.46°, 32.55°, 37.76°, 54.48°, 64.92° and 68.19°, respectively. SEM analysis indicated a mean particle size of 193.93 ± 0.23 nm for the nano-adsorbents, while EDX confirmed their elemental composition. The optimized nano-adsorbents were subjected to various applications, including the antibacterial activity, antioxidant activity, and photocatalytic dye degradation efficiency. The antibacterial activity of HA-AgO nano-adsorbents was evaluated against gram-negative (E. coli) and gram-positive (S. aureus, Lactobacillus spp.) pathogens, demonstrating broad-spectrum efficacy. The highest activity was observed against S. aureus (8 ± 0.4 mm inhibition zone), underscoring their potential to treat drug-resistent infections. Additionally, the antioxidant capacity, evaluated using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay, exhibited a radical scavenging activity of 84.36 ± 0.44%. Under UV irradiation (λ = 365 nm), the HA-AgO nano-adsorbents achieved 82.28% degradation of methylene blue (MB) dye within 120 min, demonstrating robust photocatalytic activity. Unlike conventional AgO systems, these biohybrid nano-adsorbents combine the photocatalytic efficiency of AgO with the biocompatibility and biofilm-inhibiting properties of microbially-derived HA, enabling dual functionality not achieved in single-component systems.
本研究报告了利用枯草芽孢杆菌PV154141.1合成用于环境和生物医学双重应用的透明质酸包覆氧化银(AgO)纳米吸附剂。针对HA-AgO纳米吸附剂的形成和稳定性,对多个参数进行了优化,包括硝酸银(AgNO)浓度和反应时间。采用了几种表征技术,包括X射线衍射(XRD)分析、扫描电子显微镜(SEM)和能量色散X射线(EDX)光谱,以确定合成的HA-AgO纳米吸附剂的结构性质、形态和元素组成。XRD图谱通过显示hkl值为110、111、200、220、311和222的峰,分别位于约26.46°、32.55°、37.76°、54.48°、64.92°和68.19°的2θ值处,证实了AgO纳米吸附剂的存在。SEM分析表明纳米吸附剂的平均粒径为193.93±0.23nm,而EDX证实了它们的元素组成。对优化后的纳米吸附剂进行了各种应用测试,包括抗菌活性、抗氧化活性和光催化染料降解效率。评估了HA-AgO纳米吸附剂对革兰氏阴性菌(大肠杆菌)和革兰氏阳性菌(金黄色葡萄球菌、乳酸杆菌属)病原体的抗菌活性,显示出广谱疗效。观察到对金黄色葡萄球菌的活性最高(抑菌圈为8±0.4mm),突出了它们治疗耐药感染的潜力。此外,使用2,2-二苯基-1-苦基肼(DPPH)测定法评估的抗氧化能力表现出84.36±0.44%的自由基清除活性。在紫外线照射(λ=365nm)下,HA-AgO纳米吸附剂在120分钟内实现了亚甲基蓝(MB)染料82.28%的降解,显示出强大的光催化活性。与传统的AgO系统不同,这些生物杂化纳米吸附剂将AgO的光催化效率与微生物衍生的HA的生物相容性和生物膜抑制特性结合起来,实现了单组分系统无法实现的双重功能。