School of Pharmaceutical Science, Jilin University, Changchun 130062, China.
College of Animal Science, Jilin University, Changchun 130062, China.
Molecules. 2019 Jan 28;24(3):465. doi: 10.3390/molecules24030465.
() is the primary etiological agent of dental caries. The enzyme sortase A (SrtA) is responsible for anchoring bacterial cell wall surface proteins involved in host cell attachment and biofilm formation. Thus, SrtA is an attractive target for inhibiting dental caries caused by -associated acid fermentation. In this study, we observed that astilbin, a flavanone compound extracted from , has potent inhibitory activity against the SrtA, with an IC of 7.5 μg/mL. In addition, astilbin was proven to reduce the formation of biofilm while without affecting the growth of . The results of a molecular dynamics simulation and a mutation analysis revealed that the Arg213, Leu111, and Leu116 of SrtA are important for the interaction between SrtA and astilbin. The results of this study demonstrate the potential of using astilbin as a nonbactericidal agent to modulate pathogenicity of by inhibiting the activity of SrtA.
()是龋齿的主要病因。酶天冬酰胺酰内肽酶 A(SrtA)负责锚定参与宿主细胞附着和生物膜形成的细菌细胞壁表面蛋白。因此,SrtA 是抑制与相关的酸发酵引起的龋齿的一个有吸引力的靶标。在这项研究中,我们观察到从()中提取的类黄酮化合物白杨素对具有很强的抑制活性,IC 为 7.5μg/mL。此外,白杨素被证明可以减少生物膜的形成,而不影响的生长。分子动力学模拟和突变分析的结果表明,SrtA 的 Arg213、Leu111 和 Leu116 对 SrtA 与白杨素之间的相互作用很重要。这项研究的结果表明,使用白杨素作为非杀菌剂通过抑制 SrtA 的活性来调节的致病性具有潜力。