Batchelor S E, Cooper M, Chhabra S R, Glover L A, Stewart G S, Williams P, Prosser J I
Department of Molecular and Cell Biology, University of Aberdeen, Foresterhill, United Kingdom.
Appl Environ Microbiol. 1997 Jun;63(6):2281-6. doi: 10.1128/aem.63.6.2281-2286.1997.
The speed of recovery of cell suspensions and biofilm populations of the ammonia oxidizer Nitrosomonas europaea, following starvation was determined. Stationary-phase cells, washed and resuspended in ammoniumfree inorganic medium, were starved for periods of up to 42 days, after which the medium was supplemented with ammonium and subsequent growth was monitored by measuring nitrite concentration changes. Cultures exhibited a lag phase prior to exponential nitrite production, which increased from 8.72 h (no starvation) to 153 h after starvation for 42 days. Biofilm populations of N. europaea colonizing sand or soil particles in continuous-flow, fixed column reactors were starved by continuous supply of ammonium-free medium. Following resupply of ammonium, starved biofilms exhibited no lag phase prior to nitrite production, even after starvation for 43.2 days, although there was evidence of cell loss during starvation. Biofilm formation will therefore provide a significant ecological advantage for ammonia oxidizers in natural environments in which the substrate supply is intermittent. Cell density-dependent phenomena in a number of gram-negative bacteria are mediated by N-acyl homoserine lactones (AHL), including N-(3-oxohexanoyl)-L-homoserine lactone (OHHL). Addition of both ammonium and OHHL to cell suspensions starved for 28 days decreased the lag phase in a concentration-dependent manner from 53.4 h to a minimum of 10.8 h. AHL production by N. europaea was detected by using a luxR-luxAB AHL reporter system. The results suggest that rapid recovery of high-density biofilm populations may be due to production and accumulation of OHHL to levels not possible in relatively low-density cell suspensions.
测定了欧洲亚硝化单胞菌(一种氨氧化菌)细胞悬液和生物膜群体在饥饿后的恢复速度。将处于稳定期的细胞洗涤后重悬于无铵无机培养基中,饥饿长达42天,之后向培养基中添加铵,并通过测量亚硝酸盐浓度变化来监测后续生长情况。培养物在亚硝酸盐指数产生之前表现出一个延迟期,该延迟期从8.72小时(无饥饿)增加到饥饿42天后的153小时。在连续流动固定柱反应器中定殖于沙子或土壤颗粒上的欧洲亚硝化单胞菌生物膜群体,通过持续供应无铵培养基使其饥饿。在重新供应铵之后,饥饿的生物膜在亚硝酸盐产生之前没有表现出延迟期,即使在饥饿43.2天之后也是如此,尽管有证据表明在饥饿期间细胞有损失。因此,生物膜形成将为自然环境中底物供应间歇性的氨氧化菌提供显著的生态优势。许多革兰氏阴性细菌中的细胞密度依赖性现象是由N-酰基高丝氨酸内酯(AHL)介导的,包括N-(3-氧代己酰基)-L-高丝氨酸内酯(OHHL)。向饥饿28天的细胞悬液中添加铵和OHHL,以浓度依赖的方式将延迟期从53.4小时缩短至最短10.8小时。使用luxR-luxAB AHL报告系统检测了欧洲亚硝化单胞菌产生的AHL。结果表明,高密度生物膜群体的快速恢复可能是由于OHHL的产生和积累达到了相对低密度细胞悬液中不可能达到的水平。