Firstly, the biofilm formation of AbIC IΔblp1 and AbIC IIΔblp1 mutants and their blp1-complemented strains was assessed. Bacteria were grown on the plastic surface and the formed structures were analyzed by confocal laser scanning microscopy (CLSM) using SYTO9 and propidium iodide (PI) staining as described in Materials and Methods. Interestingly, 2 h post-seeding, the initial attachment of bacteria to the plastic surface, based on the increase of PI-stained (red stain) versus total amount of bacteria (green stain) was affected in AbIC IΔblp1 mutant, demonstrating up to 55% increase in PI-stained bacteria compared with the parental strain (Fig. 2a, upper panels).
首先,對AbIC I μblp1和AbIC II+blp1突變體及其blp1互補菌株的生物膜形成進行了評估。細菌生長在塑膠表面,使用SYTO9和碘化(PI)染色(材料和方法)所述,通過共生鐳射掃描顯微鏡(CLSM)對形成結構進行分析。有趣的是,在AbIC I+bblp1突變體中,根據PI染色(紅色污漬)與細菌總量(綠色污漬)的增加,在播種后2小時,細菌最初附著在塑膠表面,與親親菌株相比,PI染色細菌增加了55%(圖2a,上面板)。