Self-assembly of metal-cholesterol oxidase hybrid nanostructures and application in bioconversion of steroids derivatives
Yu Xin , Qiuyue Gao , Yu Gu , Mengyao Hao , Guangming Fan , Liang Zhang
Front. Chem. Sci. Eng. ›› 2021, Vol. 15 ›› Issue (3) : 615 -629.
Self-assembly of metal-cholesterol oxidase hybrid nanostructures and application in bioconversion of steroids derivatives
A cholesterol oxidase (COD) was hybridized with Ca2+, Zn2+, Al3+, Fe2+ and Mn2+. After precipitation with PO43– at 4 °C for 72 h, the resulting pellets were freeze-dried. In scanning electron microscopy assays, the metal-COD complexes revealed flower-like or granular structures after hybridization. Fourier transform infrared spectroscopy assay revealed the characteristic peaks of both the enzyme and metal materials. X-ray diffraction analysis indicated that COD was encapsulated in CaHPO4·2H2O-, Zn3(PO4)2·4H2O-, AlPO4-, FeP4- and Mn3(PO4)2·3H2O-based nanostructures, respectively. Differential scanning calorimetry assay indicated significant increases in thermo-denaturation temperatures from 60.5 °C to 167.02 °C, 167.02 °C, 137.70 °C, 172.85 °C and 160.99 °C, respectively. Using steroid derivatives as substrates, this enzyme could convert cholesterol, pregnenolone, dehydroepiandrosterone, ergosterol, b-sitosterol and stigmasterol to related single products. Hybridization in metal-based nanostructures could significantly enhance the initial conversion ratio and reaction stability of the enzyme. In addition, substrate selectivity could be affected by various metal materials. Briefly, using Ca2+, Zn2+, Al3+, Fe2+ and Mn2+ as hybrid raw materials could help to encapsulate COD in related metal-enzyme nanostructures, and could help to promote the stability and tolerant properties of the enzyme, while also enhancing its catalytic characteristics.
cholesterol oxidase / metal-enzyme hybridization / nanostructures / sterol derivatives / bioconversion
Higher Education Press
Supplementary files
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