Synthesis and biological activity of a potent optically pure autoinducer-2 quorum sensing agonist

被引:8
作者
Ascenso, Osvaldo S. [1 ]
Torcato, Ines M. [1 ,2 ]
Miguel, Ana Sofia [1 ]
Marques, Joao C. [3 ]
Xavier, Karina B. [2 ]
Rita Ventura, M. [1 ]
Maycock, Christopher D. [1 ,4 ]
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, Apartado 127, P-2780901 Oeiras, Portugal
[2] Inst Gulbenkian Ciencias, P-2781901 Oeiras, Portugal
[3] Rowland Inst Harvard, 100 Edwin H Land Blvd, Cambridge, MA 02142 USA
[4] Univ Lisbon, Fac Ciencias, Dept Quim & Bioquim, P-1749016 Lisbon, Portugal
关键词
AI-2; DPD; DPD analogues; DPD agonists; Quorum sensing; AI-2; SIGNAL; COMMUNICATION;
D O I
10.1016/j.bioorg.2018.12.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Quorum sensing (QS) regulates population-dependent bacterial behaviours, such as toxin production, biofilm formation and virulence. Autoinducer-2 (AI-2) is to date the only signalling molecule known to foster interspecies bacterial communication across distantly related bacterial species. In this work, the synthesis of pure enantiomers of C4-propoxy-HPD and C4-ethoxy-HPD, known AI-2 analogues, has been developed. The optimised synthesis is efficient, reproducible and short. The (4S) enantiomer of C4-propoxy-HPD was the most active compound being approximately twice as efficient as (4S)-DPD and ten-times more potent than the (4R) enantiomer. Additionally, the specificity of this analogue to bacteria with LuxP receptors makes it a good candidate for clinical applications, because it is not susceptible to scavenging by LsrB-containing bacteria that degrade the natural AI-2. All in all, this study provides a new brief and effective synthesis of isomerically pure analogues for QS modulation that include the most active AI-2 agonist described so far.
引用
收藏
页码:75 / 81
页数:7
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