Department of Anaerobic Bacterial Vaccine Research and Production, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), P.O. Box: 31975/148, Karaj, Iran.
Department of Industrial and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), P.O. Box 1417863171, Tehran, Iran; Scion, Private Bag 3020, Rotorua 3046, New Zealand.
Enzyme Microb Technol. 2022 Mar;154:109974. doi: 10.1016/j.enzmictec.2021.109974. Epub 2021 Dec 16.
The emergence of antibiotic resistant bacteria because of the antibiotics abusement was the motivation to develop the effective alternatives to traditional antibiotics. Hence, various lysozyme corona were prepared through the physical and covalent attachment of lysozyme molecules onto either the bare or carboxyl-functionalized mesoporous silica particles. The prepared samples were characterized by STEM, TGA/DTA, zeta potential, FTIR, UV-vis and CD spectroscopic methods. All the prepared lysozyme-coated particles exhibited an efficient antibacterial activity against Listeria monocytogenes, as a case study, in vitro with no cytotoxicity. The minimal inhibition concentration (MIC) of the lysozyme-physically adsorbed bare and carboxyl-functionalized mesoporous silica nanoparticles (L-MS and L-ads-CMS, respectively) and the lysozyme-covalently attached carboxyl-functionalized MS particles (L-cov-CMS) was 2, 5.3 and 1.7 folds lower than that of the free lysozyme, respectively. Additionally, for the first time, it was reported that the pretreatment of lysozyme corona of L-ads-CMS through inducing a pH-shock can lead to the enhancement of antibacterial properties thereof. This behavior was associated to the controlled release of the immobilized lysozyme molecules and their conformational stability. These natural antibacterial lysozyme-coated silica nanoparticles showing the "pH-shock enhanced activity" could be of utmost interest for design of the highly active enzyme-modified nanoparticles.
由于抗生素滥用导致抗生素耐药菌的出现,这激发了人们开发传统抗生素有效替代品的动力。因此,通过物理和共价附着的方法将溶菌酶分子附着在裸或羧基功能化介孔硅颗粒上,制备了各种溶菌酶冠。通过 STEM、TGA/DTA、ζ电位、FTIR、UV-vis 和 CD 光谱法对制备的样品进行了表征。所有制备的溶菌酶涂层颗粒都表现出对单核细胞增生李斯特菌的高效体外抗菌活性,且无细胞毒性。溶菌酶物理吸附在裸和羧基功能化介孔硅纳米颗粒(L-MS 和 L-ads-CMS,分别)和共价附着羧基功能化 MS 颗粒(L-cov-CMS)上的溶菌酶的最小抑制浓度(MIC)分别比游离溶菌酶低 2 倍、5.3 倍和 1.7 倍。此外,这是首次报道通过诱导 pH 冲击预处理 L-ads-CMS 的溶菌酶冠可以提高其抗菌性能。这种行为与固定化溶菌酶分子的控制释放及其构象稳定性有关。这些具有“pH 冲击增强活性”的天然抗菌溶菌酶涂层硅纳米颗粒,可能对设计高活性酶修饰纳米颗粒具有重要意义。