Enzymatic basis for fungicide removal by Elodea canadensis View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-02-08

AUTHORS

Rachel Dosnon-Olette, Peter Schröder, Bernadett Bartha, Aziz Aziz, Michel Couderchet, Philippe Eullaffroy

ABSTRACT

PurposePlants can absorb a diversity of natural and man-made toxic compounds for which they have developed diverse detoxification mechanisms. Plants are able to metabolize and detoxify a wide array of xenobiotics by oxidation, sugar conjugation, glutathione conjugation, and more complex reactions. In this study, detoxification mechanisms of dimethomorph, a fungicide currently found in aquatic media were investigated in Elodea canadensis.MethodsCytochrome P450 (P450) activity was measured by an oxygen biosensor system, glucosyltransferases (GTs) by HPLC, glutathione S-transferases (GSTs), and ascorbate peroxidase (APOX) were assayed spectrophotometrically.ResultsIncubation of Elodea with dimethomorph induced an increase of the P450 activity. GST activity was not stimulated by dimethomorph suggesting that GST does not participate in dimethomorph detoxification. In plants exposed to dimethomorph, comparable responses were observed for GST and APOX activities showing that the GST was more likely to play a role in response to oxidative stress. Preincubation with dimethomorph induced a high activity of O- and N-GT, it is therefore likely that both enzymes participate in the phase II (conjugation) of dimethomorph detoxification process.ConclusionsFor the first time in aquatic plants, P450 activity was shown to be induced by a fungicide suggesting a role in the metabolization of dimethomorph. Moreover, our finding is the first evidence of dimethomorph and isoproturon activation of cytochrome P450 multienzyme family in an aquatic plant, i.e., Elodea (isoproturon was taken here as a reference molecule). The detoxification of dimetomorph seems to proceed via hydroxylation, and subsequent glucosylation, and might yield soluble as well as cell wall bound residues. More... »

PAGES

1015-1021

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11356-011-0460-1

DOI

http://dx.doi.org/10.1007/s11356-011-0460-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1012589794

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/21301975


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