Pérez-Alfaro J E, Villaseca A, Gaytán Raúl, Martínez-Jardines M A, Buitrón G, Texier A-C, Cuervo-López F M
Department of Biotechnology, Universidad Autónoma Metropolitana-Iztapalapa, Iztapalapa, CP 09310 Mexico City, México.
Unidad Académica del Instituto de Ingeniería, Universidad Nacional Autónoma de México, 76230 Querétaro, Querétaro México.
3 Biotech. 2023 Nov;13(11):364. doi: 10.1007/s13205-023-03764-z. Epub 2023 Oct 13.
Kinetic assays with a nitrifying consortium with whole nitrifying cells amended with 5 mg 2-CP-C/L and 100, 200, 300, or 500 mg NH-N/L were carried out in batch and nitrifying sequencing batch reactor (SBR) cultures. No nitrification activity was observed in batch assays with 100 mg NH-N/L and 5 mg 2-CP-C/L. Nevertheless, increasing the ammonium concentration from 200 to 500 mg NH-N/L allowed simultaneous ammonium and nitrite oxidation even in the presence of 5 mg 2-CP-C/L plus the halogenated compound consumption. Under these conditions, the ammonium monooxygenase enzyme participated in 2-CP consumption. Complete nitrification and simultaneous elimination of 5 mg 2-CP-C/L were achieved in the SBR amended with 200-500 mg NH-N/L. The inhibitory effect of 2-CP on the nitrite oxidation process completely disappeared under these conditions. Assays with nitrifying cell-free extracts, ammonium (100 mg NH-N/L), and 2-CP (5 mg 2-CP-C/L) were also conducted. In the absence of 2-CP, the nitrifying cell-free extracts maintained up to 60% of the nitrifying activity compared to whole-cells. Contrary to whole-cell assays, cell-free extracts were capable of simultaneously oxidizing ammonium and consuming 2-CP. However, the inhibitory effect of 2-CP on nitrification was still present as lower specific rates of ammonium consumption and nitrate production were obtained. Thus, these assays indicate that the presence of 2-CP affects both, the ammonium transport mechanism and the activity of nitrifying enzymes.
The online version contains supplementary material available at 10.1007/s13205-023-03764-z.
采用含有经5 mg 2-氯酚(2-CP-C)/L和100、200、300或500 mg氨氮(NH₃-N)/L修正的完整硝化细胞的硝化菌群进行动力学分析,分析在分批培养以及硝化序批式反应器(SBR)培养中进行。在含有100 mg NH₃-N/L和5 mg 2-CP-C/L的分批分析中未观察到硝化活性。然而,将铵浓度从200 mg NH₃-N/L提高到500 mg NH₃-N/L,即使在存在5 mg 2-CP-C/L以及卤代化合物消耗的情况下,也能实现铵和亚硝酸盐的同时氧化。在这些条件下,铵单加氧酶参与了2-CP的消耗。在用200 - 500 mg NH₃-N/L修正的SBR中实现了完全硝化以及5 mg 2-CP-C/L的同时去除。在这些条件下,2-CP对亚硝酸盐氧化过程的抑制作用完全消失。还进行了使用无硝化细胞提取物、铵(100 mg NH₃-N/L)和2-CP(5 mg 2-CP-C/L)的分析。在不存在2-CP的情况下,与完整细胞相比,无硝化细胞提取物保持了高达60%的硝化活性。与完整细胞分析相反,无细胞提取物能够同时氧化铵并消耗2-CP。然而,2-CP对硝化的抑制作用仍然存在,因为获得的铵消耗和硝酸盐产生的比速率较低。因此,这些分析表明2-CP的存在同时影响铵转运机制和硝化酶的活性。
在线版本包含可在10.1007/s13205-023-03764-z获取的补充材料。