Department of Biochemistry, University of Otago, Dunedin, 9054, New Zealand; Maurice Wilkins Centre for Molecular Biodiscovery, New Zealand.
Department of Biochemistry, University of Otago, Dunedin, 9054, New Zealand.
Anal Biochem. 2019 Feb 1;566:10-12. doi: 10.1016/j.ab.2018.10.029. Epub 2018 Nov 2.
N-acyl-l-homoserine lactone (AHL) acylases are a well-known group of enzymes that disrupt quorum sensing in Gram-negative bacteria by degrading AHL signalling molecules. This degradation of signalling molecules (termed 'quorum quenching') has potential uses in the prevention or reduction of biofilm formation and/or bacterial infections. Therefore, there is a great deal of interest in the identification and characterisation of quorum quenching enzymes. Here, we present an optimised fluorescamine-based assay for the detection of AHL acylase activity and demonstrate it can be used in a high-throughput screening format.
N-酰基高丝氨酸内酯 (AHL) 酰基水解酶是一类众所周知的酶,通过降解 AHL 信号分子来破坏革兰氏阴性菌的群体感应。这种信号分子的降解(称为“群体感应淬灭”)在预防或减少生物膜形成和/或细菌感染方面具有潜在的用途。因此,人们对群体感应淬灭酶的鉴定和特性研究非常感兴趣。在这里,我们提出了一种优化的荧光胺基检测 AHL 酰基水解酶活性的方法,并证明它可以用于高通量筛选格式。