Biodegradation of Aged Residues of Atrazine and Alachlor in a Mix-Load Site Soil by Fungal Enzymes
Author(s) -
Anastasia E. M. Chirnside,
William F. Ritter,
Mark Radosevich
Publication year - 2011
Publication title -
applied and environmental soil science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.431
H-Index - 23
eISSN - 1687-7675
pISSN - 1687-7667
DOI - 10.1155/2011/658569
Subject(s) - alachlor , chrysosporium , biodegradation , environmental remediation , phanerochaete , atrazine , pesticide , environmental chemistry , soil contamination , soil water , chemistry , acetanilide , contamination , environmental science , agronomy , biology , soil science , enzyme , ecology , organic chemistry
Soils from bulk pesticide mixing and loading (mix-load) sites are often contaminated with a complex mixture of pesticides, herbicides, and other organic compounds used in pesticide formulations that limits the success of remediation efforts. Therefore, there is a need to find remediation strategies that can successfully clean up these mix-load site soils. This paper examined the degradation of atrazine (2-chloro-4-ethylamino-6-isopropylamino-S-triazine; AT) and alachlor (2-chloro-2, 6-diethyl-N-[methoxymethyl]-acetanilide) in contaminated mix-load site soil utilizing an extracellular fungal enzyme solution derived from the white rot fungus, Phanerochaete chrysosporium, grown in a packed bed bioreactor. Thirty-two percent of AT and 54% of AL were transformed in the biometers. The pseudo first-order rate constant for AT and AL biodegradation was 0.0882 d−1 and 0.2504 d−1, respectively. The half-life (1/2) for AT and AL was 8.0 and 3.0 days, respectively. Compared to AT, the initial disappearance of AL proceeded at a faster rate and resulted in a greater amount of AL transformed. Based on the net Co2 evolved from the biometers, about 4% of the AT and AL initially present in the soil was completely mineralized
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