AbstractThe deamination of metribuzin was studied in vitro in peroxisomes isolated from the leaves of soybean cultivars which were either metribuzin tolerant, intermediate, or sensitive. The deamination rate observed with peroxisomes from tolerant leaves was about twice the rate observed with peroxisomes from sensitive leaves. The intermediate group was also intermediate with respect to the in‐vitro deamination rate.Tolerant and sensitive intact soybean plants were pulse‐labeled with [14C]metribuzin via the roots for 5 h. The extractable radioactivity in roots, stems and leaves was measured and separated into metabolites after the 5 h pulse and after an additional 24 h growth in water. The level of DA (deaminated metribuzin) was always significantly higher in the stems and leaves of tolerant soybean plants (4.8–10.0% of the extracted radioactivity) than in sensitive stems and leaves (1.8–2.9%). Conjugates were rapidly formed in tolerant as well as in sensitive soybean tissues. More conjugates were found in the tolerant cultivars, especially after the 5 + 24 h incubation time.Labeled [14C]DA fed to soybean plants via the roots was conjugated two to four times faster than [14C]metribuzin. Tolerant soybean tissue conjugated [14C] DA two to three times faster than sensitive tissue. The results are interpreted as showing that, in tolerant soybean plants, metribuzin is metabolized via deamination and subsequent conjugation, in addition to the well‐known direct conjugation of metribuzin parent
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