Singh Simranjeet, Kumar Vijay, Upadhyay Niraj, Singh Joginder, Singla Sourav, Datta Shivika
Department of Biotechnology, Lovely Professional University, Phagwara, Punjab 144002 India.
Regional Pesticides Testing Laboratory, Chandigarh, 160030 India.
3 Biotech. 2017 Aug;7(4):262. doi: 10.1007/s13205-017-0900-9. Epub 2017 Jul 25.
The present study was intended to investigate the biodegradation of acephate in aqueous media in the presence and in the absence of metal ions [Fe(III) and Cu(II)], and humic acid (HA). Biodegradations were performed using PS-5 (PS-5) isolated from the heavy metal polluted site. Biodegradations were monitored by UV-Visible, FTIR, and electron spray ionization-mass spectrometry (ESI-MS) analyses. ESI-MS analysis revealed that PS-5 degraded acephate to two metabolites showing intense ions at mass-to-charge ratios (/) 62 and 97. The observed kinetic was the pseudo-first order, and half-life periods () were 2.79 d (of PS-5 + acephate), 3.45 d [of PS-5 + acephate + Fe(III)], 3.16 d [of PS-5 + acephate + Cu(II)], and 5.54 d (of PS-5 + acephate + HA). A significant decrease in degradation rate of acephate was noticed in the presence of HA, and the same was confirmed by UV-Visible and TGA analyses. Strong aggregation behavior of acephate with humic acid in aqueous media was the major cause behind the slow degradation rate of acephate . New results on acephate metabolism by strain PS-5 in the presence and in the absence of metal ions [Fe(III) and Cu(II)] and humic acid were obtained. Results confirmed that strain PS-5 was capable of mineralization of the acephate without formation of toxic metabolite methamidophos. More significantly, the strain PS-5 could be useful as potential biological agents in effective bioremediation campaign for multi-polluted environments.
本研究旨在调查在有和没有金属离子[Fe(III)和Cu(II)]以及腐殖酸(HA)存在的情况下,乙酰甲胺磷在水介质中的生物降解情况。使用从重金属污染场地分离出的PS-5进行生物降解。通过紫外可见光谱、傅里叶变换红外光谱和电喷雾电离质谱(ESI-MS)分析监测生物降解过程。ESI-MS分析表明,PS-5将乙酰甲胺磷降解为两种代谢产物,其质荷比(m/z)为62和97时显示出强离子信号。观察到的动力学为假一级反应,半衰期(t1/2)分别为2.79天(PS-5 + 乙酰甲胺磷)、3.45天[PS-5 + 乙酰甲胺磷 + Fe(III)]、3.16天[PS-5 + 乙酰甲胺磷 + Cu(II)]和5.54天(PS-5 + 乙酰甲胺磷 + HA)。在HA存在的情况下,乙酰甲胺磷的降解速率显著降低,紫外可见光谱和热重分析证实了这一点。乙酰甲胺磷与腐殖酸在水介质中的强烈聚集行为是乙酰甲胺磷降解速率缓慢的主要原因。获得了关于菌株PS-5在有和没有金属离子[Fe(III)和Cu(II)]以及腐殖酸存在的情况下对乙酰甲胺磷代谢的新结果。结果证实,菌株PS-5能够使乙酰甲胺磷矿化,而不会形成有毒代谢产物甲胺磷。更重要的是,菌株PS-5可作为潜在的生物制剂用于多污染环境的有效生物修复。