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The fate and toxicity of the flavonoids naringenin and formononetin in soil
Authors:Liz J. Shaw  John E. Hooker
Affiliation:1. Department of Soil Science, The University of Reading, Whiteknights, P.O. Box 233, Reading, RG6 6DW, UK;2. Department of Environmental and Geographical Sciences, Manchester Metropolitan University, John Dalton Building, Chester Street, M1 5GD, UK
Abstract:The flavonoid class of plant secondary metabolites play a multifunctional role in below-ground plant–microbe interactions with their best known function as signals in the nitrogen fixing legume–rhizobia symbiosis. Flavonoids enter rhizosphere soil as a result of root exudation and senescence but little is known about their subsequent fate or impacts on microbial activity. Therefore, the present study examined the sorptive behaviour, biodegradation and impact on dehydrogenase activity (as determined by iodonitrotetrazolium chloride reduction) of the flavonoids naringenin and formononetin in soil. Organic carbon normalised partition coefficients, log Koc, of 3.12 (formononetin) and 3.19 (naringenin) were estimated from sorption isotherms and, after comparison with literature log Koc values for compounds whose soil behaviour is better characterised, the test flavonoids were deemed to be moderately sorbed. Naringenin (spiked at 50 μg g?1) was biodegraded without a detectable lag phase with concentrations reduced to 0.13±0.01 μg g?1 at the end of the 96 h time course. Biodegradation of formononetin proceeded after a lag phase of ~24 h with concentrations reduced to 4.5±1% of the sterile control after 72 h. Most probable number (MPN) analysis revealed that prior to the addition of flavonoids, the soil contained 5.4×106 MPN g?1 (naringenin) and 7.9×105 MPN g?1 (formononetin) catabolic microbes. Formononetin concentration had no significant (p>0.05) effect on soil dehydrogenase activity, whereas naringenin concentration had an overall but non-systematic impact (p=0.045). These results are discussed with reference to likely total and bioavailable concentrations of flavonoids experienced by microbes in the rhizosphere.
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