Abstract
The purpose of this paper is to elucidate the final degradative pathways of atrazine (I) by a Nocardia strain through experiments on the degradation of its metabolite, 4-amino-2-chloro-6-isopropylamino-1,3,5-triazine (Ha). This compound, in the bacterial medium, was transformed into several products identified as 2-chloro-4,6-diamino-1,3,5-triazine (lie), 4-amino-2-hydroxy-6-isopropylamino-1,3,5-triazine (VIII), 4-amino-1,2-dihydro-1,3,5-triazin-2-one (IV) and dicyanodi-amidine (VII). The formation of (lie) was attributed to a microbial N-dealkylation, while the detection of (IV) and (VII) was attributed to a chemical degradation of the intermediate 4-amino-2-chloro-1,3,5-triazine (III). Compound (III) undergoes rapid hydrolysis and does not accumulate in the culture medium. On the basis of the microbial and chemical results, we propose a degradative pathway for atrazine. © 1985, Japan Society for Bioscience, Biotechnology, and Agrochemistry. All rights reserved.
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CITATION STYLE
Filacchioni, G., & Giardina, M. C. (1985). Chemical and Biological Degradation of Primary Metabolites of Atrazine by a Nocardia Strain. Agricultural and Biological Chemistry, 49(6), 1551–1558. https://doi.org/10.1271/bbb1961.49.1551
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