Kim A-Leum, Park Son-Young, Lee Chi-Ho, Lee Chung-Hak, Lee Jung-Kee
Department of Biomedicinal Science and Biotechnology, Paichai University, Daejeon 302-735, Republic of Korea.
J Microbiol Biotechnol. 2014 Nov 28;24(11):1574-82. doi: 10.4014/jmb.1407.07009.
Bacteria recognize changes in their population density by sensing the concentration of signal molecules, N-acyl-homoserine lactones (AHLs). AHL-mediated quorum sensing (QS) plays a key role in biofilm formation, so the interference of QS, referred to as quorum quenching (QQ), has received a great deal of attention. A QQ strategy can be applied to membrane bioreactors (MBRs) for advanced wastewater treatment to control biofouling. To isolate QQ bacteria that can inhibit biofilm formation, we isolated diverse AHL-degrading bacteria from a laboratory-scale MBR and sludge from real wastewater treatment plants. A total of 225 AHLdegrading bacteria were isolated from the sludge sample by enrichment culture. To identify the enzyme responsible for AHL degradation in QQ bacteria, AHL-degrading activities were analyzed using cell-free lysate, culture supernatant, and whole cells. Afipia sp. and Acinetobacter sp. strains produced the intracellular QQ enzyme, whereas Pseudomonas sp. and Micrococcus sp. produced the extracellular QQ enzyme that was most likely to produce AHLacylase. AHL-degrading activity was observed in whole-cell assay with the Microbacterium sp. and Rhodococcus sp. strains. There has been no report for AHL-degrading capability in the case of Streptococcus sp. and Afipia sp. strains. Finally, inhibition of biofilm formation by isolated QQ bacteria or enzymes was observed on glass slides and 96-well microtiter plates using crystal violet staining. QQ strains or enzymes not only inhibited initial biofilm development but also reduced established biofilms.
细菌通过感知信号分子N-酰基高丝氨酸内酯(AHLs)的浓度来识别其种群密度的变化。AHL介导的群体感应(QS)在生物膜形成中起关键作用,因此,群体感应干扰(QQ)受到了广泛关注。一种QQ策略可应用于膜生物反应器(MBR)进行深度废水处理以控制生物污染。为了分离出能够抑制生物膜形成的QQ细菌,我们从实验室规模的MBR和实际污水处理厂的污泥中分离出了多种AHL降解细菌。通过富集培养从污泥样品中总共分离出225株AHL降解细菌。为了鉴定QQ细菌中负责AHL降解的酶,使用无细胞裂解液、培养上清液和全细胞分析了AHL降解活性。阿菲波尼亚菌属和不动杆菌属菌株产生细胞内QQ酶,而假单胞菌属和微球菌属产生最有可能产生AHL酰基酶的细胞外QQ酶。在对微杆菌属和红球菌属菌株的全细胞测定中观察到了AHL降解活性。对于链球菌属和阿菲波尼亚菌属菌株的AHL降解能力尚无报道。最后,使用结晶紫染色在载玻片和96孔微量滴定板上观察到分离出的QQ细菌或酶对生物膜形成的抑制作用。QQ菌株或酶不仅抑制了初始生物膜的形成,还减少了已形成的生物膜。