Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon 97331.
Appl Environ Microbiol. 1998 Apr;64(4):1514-21. doi: 10.1128/AEM.64.4.1514-1521.1998.
The effects of limiting concentrations of ammonium on the metabolic activity of Nitrosomonas europaea, an obligate ammonia-oxidizing soil bacterium, were investigated. Cells were harvested during late logarithmic growth and were incubated for 24 h in growth medium containing 0, 15, or 50 mM ammonium. The changes in nitrite production and the rates of ammonia- and hydroxylamine-dependent oxygen consumption were monitored. In incubations without ammonium, there was little change in the ammonia oxidation activity after 24 h. With 15 mM ammonium, an amount that was completely consumed, there was an 85% loss of the ammonia oxidation activity after 24 h. In contrast, there was only a 35% loss of the ammonia oxidation activity after 24 h in the presence of 50 mM ammonium, an amount that was not consumed to completion. There was little effect on the hydroxylamine oxidation activity in any of the incubations. The loss of ammonia oxidation activity was not due to differences in steady-state levels of ammonia monooxygenase (AMO) mRNA (amoA) or to degradation of the active site-containing subunit of AMO protein. The incubations were also conducted at a range of pH values to determine whether the loss of ammonia oxidation activity was correlated to the residual ammonium concentration. The loss of ammonia oxidation activity after 24 h was less at lower pH values (where the unoxidized ammonium concentration was higher). When added in conjunction with limiting ammonium, short-chain alkanes, which are alternative substrates for AMO, prevented the loss of ammonia oxidation activity at levels corresponding to their binding affinity for AMO. These results suggest that substrates of AMO can preserve the ammonia-oxidizing activity of N. europaea in batch incubations by protecting either AMO itself or other molecules associated with ammonia oxidation.
研究了限制铵浓度对专性氨氧化土壤细菌硝化单胞菌(Nitrosomonas europaea)代谢活性的影响。在对数生长期后期收获细胞,并在含有 0、15 或 50mM 铵的生长培养基中孵育 24 小时。监测亚硝酸盐生成的变化和氨及羟胺依赖的耗氧速率。在没有铵的孵育中,24 小时后氨氧化活性几乎没有变化。在完全消耗的 15mM 铵存在下,24 小时后氨氧化活性损失 85%。相比之下,在存在 50mM 铵(未完全消耗)的情况下,24 小时后氨氧化活性仅损失 35%。在任何孵育中,羟胺氧化活性都没有受到影响。氨氧化活性的丧失不是由于氨单加氧酶(AMO)mRNA(amoA)的稳态水平的差异或 AMO 蛋白活性位点包含的亚基的降解所致。还在一系列 pH 值下进行了孵育,以确定氨氧化活性的丧失是否与残留的铵浓度相关。在较低的 pH 值(未氧化的铵浓度较高)下,24 小时后氨氧化活性的丧失较少。当与限制的铵一起添加时,短链烷烃(AMO 的替代底物)在与 AMO 的结合亲和力相对应的水平上防止了氨氧化活性的丧失。这些结果表明,AMO 的底物可以通过保护 AMO 本身或与氨氧化相关的其他分子来保持硝化单胞菌的氨氧化活性。