TR activity was determined in 200 μl reactions using 10 μl of cell free extract in buffer 50 mM Tris-HCl (pH 7.4), 1 mM tellurite, 1 mM NAD(P)H (Sigma-Aldrich) and 1 mM β-mercaptoethanol (Sigma-Aldrich). TR activity was monitored following the appearance of tellurium at 500 nm as described previously57 (link). One unit (U) of TR activity was defined as the amount of enzyme required to increase the OD 500 nm in 0.001 min−1 mg protein−1.
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