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Open AccessJournal ArticleDOI

A Negative Effect of Co-solvent on Atrazine Biodegradation in Experimental River Microcosms

Koji Satsuma, +3 more
- 01 Sep 2001 - 
- Vol. 16, Iss: 3, pp 185-189
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TLDR
In this paper, a 0.1% concentration of acetonitrile as a co-solvent greatly suppressed the microbial degradation of herbicide atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino]-s-triazine] throughout the experimental period (84 days).
Abstract
A water-miscible solvent, such as acetone, acetonitrile or methanol, is often employed as a co-solvent to dissolve an organic test chemical of low water solubility in an environmental fate study using a laboratory model microcosm. These co-solvents, however, may disrupt the microflora in the water/sediment tested, and affect the biodegradation of the target compound. In the present study, a 0.1% concentration of acetonitrile as a co-solvent greatly suppressed the microbial degradation of herbicide atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine] throughout the experimental period (84 days). The rapid growth of specific microbes was considered to deprive atrazine-degrading microbes of their habitat (mainly the surface area of sediment particles) in the microcosm.

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Citations
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Journal ArticleDOI

Characterisation of new strains of atrazine-degrading Nocardioides sp. isolated from Japanese riverbed sediment using naturally derived river ecosystem.

TL;DR: Atrazine biodegradation in the microcosm appeared to occur predominantly by Nocardioides sp.
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Tolerancia de hongos filamentosos a endosulfán, clorpirifós y clorotalonil en condiciones in vitro

TL;DR: Four fungal strains are good candidates for being used for pesticide bioremediation because they have acceptable tolerance to the three pesticides comparable to PC, TV and TRI.
Journal ArticleDOI

Role and Behavior of Benthic Microbes Able to Degrade Herbicide Atrazine in Naturally Derived Water/sediment Microcosm

TL;DR: In this paper, a simple laboratory microcosm constituted of riverbed sediment and its associated water, rapid degradation of herbicide atrazine mainly to cyanuric acid occurred through microbial degradation.
Journal ArticleDOI

Introduction of 2,4-dichlorophenoxyacetic acid into soil with solvents and resulting implications for bioavailability to microorganisms

TL;DR: In this article, the authors investigate relative effects of carrier solvent choice and volume on xenobiotic distribution, apparent solvent toxicity, and soil degradation of 2,4-dichlorophenoxy acetic acid.
References
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Journal ArticleDOI

Degradation and mineralization of atrazine by a soil bacterial isolate.

TL;DR: This is the first report of a pure bacterial isolate with the ability to cleave the s-triazine ring structure of atrazine, and it was concluded that this bacterium was capable of dealkylation, dechlorination, and deamination in addition to ring cleavage.
Journal ArticleDOI

s-Triazines as nitrogen sources for bacteria

TL;DR: In this paper, three strains of Pseudomonas (A, D, and F) and two strains of Klebsiella pneumoniae (90 and 99) were examined, and specific growth rates with s-triazines were similar to those with ammonium ion as the nitrogen source.
Journal ArticleDOI

Ring cleavage and degradative pathway of cyanuric acid in bacteria.

TL;DR: Data indicate that the same pathway occurred in another pseudomonad and a strain of Klebsiella pneumoniae, and each substrate was entirely metabolized concomitantly with growth.
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