Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.
Department of Protein Science, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, AlbaNova University Center, Stockholm, Sweden.
Microbiologyopen. 2020 Apr;9(4):e993. doi: 10.1002/mbo3.993. Epub 2020 Feb 7.
Bacteria forming biofilms on surgical implants is a problem that might be alleviated by the use of antibacterial coatings. In this article, recombinant spider silk was functionalized with the peptidoglycan degrading endolysin SAL-1 from the staphylococcal bacteriophage SAP-1 and the biofilm-matrix-degrading enzyme Dispersin B from Aggregatibacter actinomycetemcomitans using direct genetic fusion and/or covalent protein-protein fusion catalyzed by Sortase A. Spider silk assembly and enzyme immobilization was monitored using quartz crystal microbalance analysis. Enzyme activity was investigated both with a biochemical assay using cleavage of fluorescent substrate analogues and bacterial assays for biofilm degradation and turbidity reduction. Spider silk coatings functionalized with SAL-1 and Disperin B were found to exhibit bacteriolytic effect and inhibit biofilm formation, respectively. The strategy to immobilize antibacterial enzymes to spider silk presented herein show potential to be used as surface coatings of surgical implants and other medical equipment to avoid bacterial colonization.
细菌在外科植入物上形成生物膜是一个问题,使用抗菌涂层可能会缓解这个问题。在本文中,通过使用葡萄球菌噬菌体 SAP-1 的肽聚糖降解内切酶 SAL-1 和Aggregatibacter actinomycetemcomitans 的生物膜基质降解酶 Dispersin B 对重组蜘蛛丝进行了功能化,使用直接遗传融合和/或 Sortase A 催化的共价蛋白-蛋白融合。使用石英晶体微天平分析监测蜘蛛丝组装和酶固定化。使用荧光底物类似物的生化测定和用于生物膜降解和浊度降低的细菌测定来研究酶活性。发现用 SAL-1 和 Disperin B 功能化的蜘蛛丝涂层具有溶菌作用,并分别抑制生物膜形成。将抗菌酶固定到蜘蛛丝上的策略显示出有可能被用作外科植入物和其他医疗器械的表面涂层,以避免细菌定植。