Departament of Biotechnology and Bioengineering, Center of Research and Advanced Studies of the National Polytechnic Institute, México.
J Environ Sci Health B. 2009 Nov;44(8):798-804. doi: 10.1080/03601230903238368.
The purpose of this work was to demonstrate that a Fenton (H(2)O(2)/Fe) reaction was involved in DDT [1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane)] degradation in a culture of Penicillium sp. spiked with FeSO(4). A commercial DDT mixture (10% DDE [1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene], 30% o,p-DDT and 60% of p,p' -DDT) of 10 mg L(-1) was used. Hydrogen peroxide (H(2)O(2)), tartaric acid and oxalic acid were identified at 18 h in culture media, with and without added DDT; this correlated positively with lowering of pH from 5.8 to 2.7. Lower concentrations of oxalic acid and H(2)O(2) (7.9 and 52.6 mg L(-1), respectively) occurred in media with DDT at 30 h, in comparison to that one without DDT mixture (27.9 and 65.3 mg L(-1), respectively), at this time there was maximum degradation (87.7, 91.7 and 94.2%) for DDE, o,p-DDT and p,p'-DDT, respectively. We propose that the degradation of the DDT mixture by Penicillium sp. was through a Fenton reaction (H(2)O(2)/Fe) under acidic conditions produced in situ during the fungal culture amended with FeSO(4).
本研究旨在证明在添加了 FeSO4 的青霉菌培养物中,DDT(1,1,1-三氯-2,2-双(对氯苯基)乙烷)的降解涉及 Fenton(H2O2/Fe)反应。使用了浓度为 10mg/L 的商用 DDT 混合物(10%DDE[1,1-二氯-2,2-双(对氯苯基)乙烯]、30%o,p-DDT 和 60%p,p'-DDT)。在添加和不添加 DDT 的培养基中,在 18 小时时鉴定出了过氧化氢(H2O2)、酒石酸和草酸;这与 pH 值从 5.8 降低到 2.7 呈正相关。在添加 DDT 的培养基中,草酸和 H2O2 的浓度分别为 7.9 和 52.6mg/L,而在不含 DDT 混合物的培养基中,草酸和 H2O2 的浓度分别为 27.9 和 65.3mg/L,在 30 小时时发生了最大降解(分别为 DDE、o,p-DDT 和 p,p'-DDT 的 87.7%、91.7%和 94.2%)。我们提出,青霉菌对 DDT 混合物的降解是通过在添加了 FeSO4 的真菌培养物中产生的原位 Fenton 反应(H2O2/Fe)进行的。