A Cyclic Dipeptide from Marine Fungus Penicillium chrysogenum DXY-1 Exhibits Anti-quorum Sensing Activity

被引:24
|
作者
Yu, Xiaodan [1 ]
Li, Li [1 ]
Sun, Shiwei [2 ]
Chang, Aiping [1 ]
Dai, Xiaoyun [3 ]
Li, Hui [3 ]
Wang, Yinglu [1 ]
Zhu, Hu [1 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci,Engn Res Ctr Ind Biocatalysis, Minist Educ,Fujian Prov Key Lab Polymer Mat,Fujia, Fujian Prov Univ,Key Lab OptoElect Sci & Technol, Fuzhou 350007, Peoples R China
[2] Qingdao Univ, Sch Pharm, Dept Nat Med & Pharmacognosy, Qingdao 266071, Peoples R China
[3] China Univ Petr East China, Ctr Bioengn & Biotechnol, Qingdao 266580, Peoples R China
来源
ACS OMEGA | 2021年 / 6卷 / 11期
关键词
D O I
10.1021/acsomega.1c00020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bacterial quorum sensing (QS) is anticipated as a new potential target for the development of antimicrobial drugs. An anti-QS substance against Chromobacterium violaceum CV026 and Pseudomonas aeruginosa PA01 has been isolated and purified from the crude extracts of the marine fungus Penicillium chrysogenum DXY-1, and the accurate structure was identified as cyclo(L-Tyr-L-Pro). This cyclic dipeptide at sub-minimum inhibitory concentration can decrease the QS-regulated violacein production of C. violaceum CV026 by 79% and QS-mediated pyocyanin production, proteases, and elastase activity of P. aeruginosa PA01 by 41%, 20%, and 32%, respectively. In addition, it can also destroy the biofilm formation and decrease QS gene expression of P. aeruginosa PA01. Molecular docking was further performed, and the obtained data indicated that this dipeptide blocks the effect of QS autoinducers through competitive binding to the same pocket of the receptor proteins. We expect this anti-QS cyclic dipeptide to be a potential pro-drug treating drug-resistant P. aeruginosa infections, and these findings could relieve the alarming problem of microbial resistance to antimicrobial drugs.
引用
收藏
页码:7693 / 7700
页数:8
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