Zeng Zhirui, Qian Li, Cao Lixiang, Tan Hongming, Huang Yali, Xue Xiaoli, Shen Yong, Zhou Shining
State Key Laboratory for Biocontrol, School of Life Sciences, Zhongshan (Sun Yat-Sen) University, Guangzhou, PR China.
Appl Microbiol Biotechnol. 2008 May;79(1):119-26. doi: 10.1007/s00253-008-1406-5. Epub 2008 Mar 11.
The automated docking program DOCK 5.3.0 was applied to screening for quorum sensing inhibitors (QSIs) of Peudomonus aeruginosa from a database containing 51 active components of Traditional Chinese Medicines with antibacterial activity. Five potential QSIs were revealed by the computer-based virtual screening. The compounds 3, 4, 5, 6, 7 inhibit biofilm formation of P. aeruginosa at a concentration of 200 microM. Compound 4 (baicalein) does not inhibit the growth of P. aeruginosa; however, it significantly inhibits biofilm formation of the bacteria at a lower concentration of 20 microM and promoted proteolysis of the signal receptor TraR protein in Escherichia coli at 4-40 mM. Baicalein and ampicillin showed synergistic activity against P. aeruginosa. These results suggested that baicalein can interfere with quorum sensing system of P. aeruginosa and will be developed as antibacterial agent with novel target.
运用自动对接程序DOCK 5.3.0,从包含51种具有抗菌活性的中药活性成分的数据库中筛选铜绿假单胞菌群体感应抑制剂(QSIs)。通过基于计算机的虚拟筛选揭示了5种潜在的QSIs。化合物3、4、5、6、7在200微摩尔浓度下可抑制铜绿假单胞菌生物膜形成。化合物4(黄芩素)不抑制铜绿假单胞菌生长;然而,它在20微摩尔的较低浓度下能显著抑制该菌生物膜形成,并在4至40毫摩尔浓度下促进大肠杆菌中信号受体TraR蛋白的蛋白水解。黄芩素和氨苄西林对铜绿假单胞菌表现出协同活性。这些结果表明黄芩素可干扰铜绿假单胞菌的群体感应系统,并将被开发为具有新型靶点的抗菌剂。