Tahmasebi Aminallah, Ganbaatar Byambasuren, Bakhshi Somayeh, Yun Hyosuk, Lee Chul Won
Department of Chemistry, Chonnam National University, Gwangju, Republic of Korea; Department of Agriculture, Minab Higher Education Center, University of Hormozgan, Bandar Abbas, Iran.
Department of Chemistry, Chonnam National University, Gwangju, Republic of Korea.
Int J Biol Macromol. 2025 Sep;321(Pt 3):146402. doi: 10.1016/j.ijbiomac.2025.146402. Epub 2025 Jul 31.
Endophytic fungi have emerged as valuable reservoirs for discovering bioactive compounds with significant biological properties. In this study, a novel endophytic fungus, Talaromyces pinophilus 47 K9, was isolated from Prosopis stephaniana. The antimicrobial enzyme glucose oxidase was purified from the culture medium of T. pinophilus 47 K9 through a series of techniques, including 70 % ammonium sulfate precipitation, solid-phase extraction, ultrafiltration, ion-exchange chromatography, and gel filtration. The enzyme was identified using SDS-PAGE and proteomic analysis via MS/MS sequencing. Biochemical characterization revealed a molecular weight of 65.8 kDa and an enzymatic activity of 0.71 U/mL when glucose served as a substrate. The glucose oxidase demonstrated broad stability within a pH range of 3 to 10, though it was thermally unstable at temperatures exceeding 60 °C. Substrate specificity tests indicated that glucose served as the optimal substrate for H₂O₂ production, which subsequently improved antimicrobial efficacy. Notably, the glucose oxidase exhibited broad-spectrum antimicrobial activity, effectively inhibiting five Candida species, six phytopathogenic fungi, and both Gram-positive and Gram-negative bacteria. Given its potent antimicrobial properties, high substrate specificity, and stability across diverse conditions, glucose oxidase from T. pinophilus 47 K9 holds potential as a viable alternative antimicrobial agent.
内生真菌已成为发现具有重要生物学特性的生物活性化合物的宝贵资源库。在本研究中,从斯蒂芬牧豆树中分离出一种新型内生真菌嗜松青霉47 K9。通过一系列技术,包括70%硫酸铵沉淀、固相萃取、超滤、离子交换色谱和凝胶过滤,从嗜松青霉47 K9的培养基中纯化出抗菌酶葡萄糖氧化酶。通过SDS-PAGE和基于MS/MS测序的蛋白质组学分析对该酶进行鉴定。生化特性表明,以葡萄糖为底物时,其分子量为65.8 kDa,酶活性为0.71 U/mL。葡萄糖氧化酶在pH值3至10的范围内表现出广泛的稳定性,不过在温度超过60°C时热不稳定。底物特异性测试表明,葡萄糖是产生H₂O₂的最佳底物,这随后提高了抗菌效果。值得注意的是,葡萄糖氧化酶表现出广谱抗菌活性,有效抑制了五种念珠菌、六种植物病原真菌以及革兰氏阳性菌和革兰氏阴性菌。鉴于其强大的抗菌特性以及在不同条件下的高底物特异性和稳定性,嗜松青霉47 K9的葡萄糖氧化酶有望成为一种可行的替代抗菌剂。