Supporting Information
Organotellurium-bridged cyclodextrin dimers as Artificial Glutathione Peroxidase models
Aiquan Jiaoa,b, Na Yang a,b, Jinpeng Wang a,b, Alhassane Toure a,b, Xueming Xu a,b, and Zhengyu Jina,b,
aThe State Key Laboratory of Food Science and Technology and bSchool of Food Science and Technology, Jiangnan University, 1800 Lihu Road, Wuxi 214122, China
*Corresponding author ()
- Kinetic Study of Peroxidase Reaction of 2-TeCD (Fig.1-10)
Fig. 1Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[H2O2] (mM-1) for 2-Te-α-CD (2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig. 2Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[GSH] (mM-1) for 2-Te-α-CD(2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig. 3Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[t-BuOOH] (mM-1) for 2-Te-α-CD(2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig. 4Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[GSH] (mM-1) for 2-Te-α-CD(2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig. 5Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[H2O2] (mM-1) for 2-Te-γ-CD (2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig.6Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[GSH] (mM-1) for 2-Te-γ-CD(2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig.7Lineweaver-Burk plotsof [E]0/v0 (min) vs 1/[t-BuOOH] (mM-1) for 2-Te-γ-CD (2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig.8Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[GSH] (mM-1) for 2-Te-γ-CD (2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig.9Lineweaver-Burk plots of [E]0/v0 (min) vs 1/[CuOOH] (mM-1) for 2-Te-γ-CD (2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
Fig.10Lineweaver-Burk plotsof [E]0/v0 (min) vs 1/[GSH] (mM-1) for 2-Te-γ-CD (2μM), in 50 mM potassium phosphate buffer, pH 7.0, and 37 °C.
2. 1H NMR Study on the Inclusion Complex of GSH with2-Te-γ-CD (Fig. 11-13)
Fig.111H NMR spectra as a function of molar ratios of GSH/2-Te-γ-CD ranging from 1:0 (a) to 1:9 (j) at room temperature.
Fig. 12 Curve-fitting analysis of the differential shift of H5 proton of GSH (Δδobs) to calculate stoichiometry and the complex stability constant (Kc) upon addition of 2-Te-γ-CD (0–9 mM) in D2O at temperature.
Fig. 13 Plots of the shift values of the H5 signal of GSH by adding2-Te-γ-CD versus the molar concentration ratio of 2-Te-γ-CD to GSH atroom temperature.
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