College of Food Science and Technology, Shanghai Ocean University, 999# Hu Cheng Huan Road, Shanghai 201306, China.
Food Quality Supervision and Testing Center of the Ministry of Agriculture and Rural Affairs (Shanghai), Shanghai Center of Agri-Products Quality and Safety, Shanghai 201708, China.
Int J Mol Sci. 2022 Nov 18;23(22):14352. doi: 10.3390/ijms232214352.
The localization of lipoprotein (Lol) system is responsible for the transport of lipoproteins in the outer membrane (OM) of . LolB catalyzes the last step in the Lol system, where lipoproteins are inserted into the OM. If the function of LolB is impeded, growth of is inhibited, due to lack of an intact OM barrier for protection against the external environment. Additionally, it becomes progressively harder to generate antimicrobial resistance (AMR). In this study, LolB was employed as the receptor for a high-throughput virtual screening from a natural compounds database. Compounds with higher glide score were selected for an inhibition assay against . It was found that procyanidin, stevioside, troxerutin and rutin had both exciting binding affinity with LolB in the micromolar range and preferable antibacterial activity in a concentration-dependent manner. The inhibition rates of 100 ppm were 87.89%, 86.2%, 91.39% and 83.71%, respectively. The bacteriostatic mechanisms of the four active compounds were explored further via fluorescence spectroscopy and molecular docking, illustrating that each molecule formed a stable complex with LolB via hydrogen bonds and pi-pi stacking interactions. Additionally, the critical sites for interaction with LolB, Tyr108 and Gln68, were also illustrated. This paper demonstrates the inhibition of LolB, thus, leading to antibacterial activity, and identifies LolB as a promising drug target for the first time. These compounds could be the basis for potential antibacterial agents against .
脂蛋白(Lol)系统的定位负责脂蛋白在 的外膜(OM)中的转运。LolB 催化 Lol 系统的最后一步,即脂蛋白插入 OM。如果 LolB 的功能受到阻碍,由于缺乏完整的 OM 屏障来保护免受外部环境的影响, 的生长会受到抑制。此外,产生抗菌药物耐药性(AMR)的难度也会越来越大。在这项研究中,LolB 被用作从天然化合物数据库中进行高通量虚拟筛选的受体。选择具有更高滑行分数的化合物进行针对 的抑制测定。结果发现,原花青素、甜菊苷、曲克芦丁和芦丁在微摩尔范围内与 LolB 具有令人兴奋的结合亲和力,并且在浓度依赖性方式下具有更好的抗菌活性。100ppm 的抑制率分别为 87.89%、86.2%、91.39%和 83.71%。通过荧光光谱和分子对接进一步探索了这四种活性化合物的抑菌机制,表明每个分子都通过氢键和 π-π 堆积相互作用与 LolB 形成稳定的复合物。此外,还说明了与 LolB 相互作用的关键位点 Tyr108 和 Gln68。本文首次证明了 LolB 的抑制作用,从而导致抗菌活性,并确定 LolB 作为一种有前途的药物靶点。这些化合物可能是针对 的潜在抗菌剂的基础。