Aspergillus sydowii CBMAI 935 |
32%, 80% and 52% of chlorpyrifos, methyl parathion, and profenofos, respectively |
2% malt liquid medium with 50 mg·L−1 of chlorpyrifos, methyl parathion or profenofos incubated for 30 days at 32 °C and 130 rpm |
chlorpyrifos degradation resulted in tetraethyl dithiodi- phosphate and 2,3,5-trichloro-6-methoxypyridine; methyl parathion hydrloyzed into methylated phosphate and phosphorothioates, and 1-methoxy-4-nitrobenzen; profenofos degraded into 4-bromo-2-chloro-1-methoxybenzen and O,O-diethyl-S-proyl phosphorothioates |
Soares et al. [27] |
Aspergillus sydowii CBMAI 935, Penicillium decaturense CBMAI 1234 |
80% |
liquid mineral medium supplemented with KNO3 and 100 mg·L−1 of methyl parathion incubated for 30 days at 32 °C and 130 rpm |
p-nitrophenol |
Alvarenga et al. [28] |
Aspergillus niger AN400 |
2% (glucose-free treatment, initial concentration of methyl parathion was 19.1 mg·L−1), 43% (glucose-treated medium, initial concentration of methyl parathion 24.9 mg·L−1) |
glucose-free or glucose treated distilled water supplemented with Vishniac solution and up to 24.9 mg·L−1 of methyl parathion incubated for 27 days at 30 °C and 200 rpm |
not reported |
Marinho et al. [29] |
Penicillium citrinum, (Fusarium proliferatum) |
complete degradation (the biotic control had the same degradation efficiency) |
3% malt liquid medium with 30 mg·L−1 of methyl parathion incubated for 30 days at 32 °C and 130 rpm |
not reported |
Rodrigues et al. [30] |
Aspergillus niger MRU01 |
70%, 54%, 58%, and 68% of malathion, parathion, chlorpyrifos and dimethoate, respectively |
Czapek–Dox broth spiked with 500, 470, 260 and 680 μmol·L−1 (0.5%) of malathion, parathion, chlorpyrifos, and dimethoate, respectively, incubated for 5 days at 26 °C and 120 rpm (optimum at pH 4) |
not reported |
Mohapatra et al. [31] |
Aspergillus flavus |
complete degradation |
mineral salt medium supplemented with 5 mg·L−1 of malathion incubated for 36 days at 30 °C (pH 7) on a rotatory shaker (optimized conditions) |
not reported |
Derbalah et al. [32] |
Aspergillus sp. F1 |
over 90% (89% at an inlet load of 180 mg·L−1·d−1) |
bioreactor supplemented with 300 mg·L−1 of chlorpyrifos as the sole carbon source incubated at 28 °C (pH 7) with dissolved oxygen concentration of 5.8 mg·L−1 (optimized conditions) |
not reported |
Yadav et al. [33] |
Aspergillus fumigatus |
99% |
potato dextrose broth supplemented with chlorpyrifos (10%) incubated for 9 days at 25 °C (pH 7) and 180 rpm |
not reported |
Anggreini et al. [34] |
Aspergillus fumigatus |
95.9% |
potato dextrose broth with chlorpyrifos (1.5%) incubated for 5 days at 25 °C (pH 7) and 180 rpm |
not reported |
Anggreini et al. [35] |
Aspergillus terreus JAS1 |
complete degradation (after 24 h) |
M1 medium supplemented with 300 mg·L−1 of chlorpyrifos as the sole carbon source incubated for 96 h at 30 °C and 120 rpm |
3,5,6-trichloropyridin-2-ol that was completely degraded after 48 h; no other metabolites were reported |
Silambarasan and Abraham [36] |
Aspergillus oryzae strains AM1 and AM2 |
73% (AM1), 50% (AM2) |
Czapek–Dox broth spiked with 20 mg·L−1 of chlorpyrifos incubated for 30 days at 25 °C and 60 rpm (optimum at pH 4) |
not reported |
Barberis et al. [37] |
Aspergillus viridinutans, Penicillium implicatum |
44.6% (A. viridinutans), 16.2% (P. implicatum) |
potato dextrose broth with 20 mg·L−1 of chlorpyrifos incubated for 14 days at 28 °C |
not reported; high losses of chlorpyrifos from culture medium were due to abiotic hydrolysis |
Abdel-Wareth and Abd El-Hamid [38] |
Aspergillus niger, (Trichoderma viride) |
72.3%, (95.7%) |
Czapek–Dox broth spiked with 1.25 mg·L−1 of chlorpyrifos incubated for 14 days at 30 °C and intermittent shaking (pH 6.8) |
not reported; high losses of chlorpyrifos from culture medium were due to abiotic hydrolysis |
Mukherjee and Gopal [39] |
Penicillium citrinum, Aspergillus niger, Aspergillus oryzae |
25.9% (P. citrinum), 64% (A. niger), 50.8% (A. oryzae) |
Burkes mineral broth with 10 mg·L−1 of chlorpyrifos incubated for 15 days at 27 °C without shaking (pH 7.2) |
not reported; high losses of chlorpyrifos from culture medium were due to abiotic hydrolysis |
Abd-Alrahman and Mostafa [40] |
Aspergillus niger |
~80% |
soil extract medium with 10 mg·L−1 of chlorpyrifos incubated for 30 days at 25 °C and 60 rpm |
3,5,6-trichloro-2-pyridinol were detected below the concentration of 1 mg·L−1 |
Karas et al. [41] |
Aspergillus fumigatus, A. flavus, A. niger, A. ochraceus, A. tamarii, A. terreus, Penicillium chrysogenum, P. brevicompactum, P. citrinum, P. funiculosum |
phosphor mineralization efficiencies ranged from 4 to 46% (Cyolan), from 9.5 to 26.8% (Malathion), and from 2.3 to 6.7% (Dursban) |
Czapek–Dox broth spiked with 100 mg·L−1 of cyolan, malathion, and chlorpyrifos incubated for 35 days at 28 °C without shaking |
not reported; media and biomass were analyzed for phosphor and sulfur that mineralized from the degradation of insecticide |
Omar [42] |
Penicillium oxalicum ZHJ6 |
complete degradation |
mineral salt medium with 1% glucose supplemented with 1 mg·L−1 of methamidophos as sole nitrogen source incubated for 12 days at 25 °C and pH of 5.0 (most favorable conditions) |
inorganic phosphor, CH3SH, and CH3OH are hypothesized being formed |
Zhao et al. [43] |
Aspergillus oryzae A-F02 |
~13.7% |
fermentation medium with 1.5 g·L−1 of glyphosate incubated for 144 h at 30 °C and 150 rpm |
aminomethylphosphonic acid and methylamine, the latter being further degraded |
Fu et al. [44] |