Encapsulation of Microperoxidase‑8 in MIL-101(Cr)‑X Nanoparticles: Influence of Metal–Organic Framework Functionalization on Enzymatic Immobilization and Catalytic Activity

Microperoxidase 8 (MP8) was immobilized within MIL-101­(Cr) bearing terephthalate linkers with functionalized groups (-NH2 and -SO3H). A synthesis protocol for MIL-101­(Cr)-SO3H that avoids the use of toxic Cr­(VI) and HF was developed. The electrostatic interactions between the MP8 molecules and th...

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Veröffentlicht in:ACS applied nano materials 2020-04, Vol.3 (4), p.3233-3243
Hauptverfasser: Gkaniatsou, Effrosyni, Ricoux, Rémy, Kariyawasam, Kalani, Stenger, Ingrid, Fan, Benhui, Ayoub, Narjès, Salas, Samanta, Patriarche, Gilles, Serre, Christian, Mahy, Jean-Pierre, Steunou, Nathalie, Sicard, Clémence
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Sprache:eng
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Zusammenfassung:Microperoxidase 8 (MP8) was immobilized within MIL-101­(Cr) bearing terephthalate linkers with functionalized groups (-NH2 and -SO3H). A synthesis protocol for MIL-101­(Cr)-SO3H that avoids the use of toxic Cr­(VI) and HF was developed. The electrostatic interactions between the MP8 molecules and the MOF matrices were found to be crucial for a successful immobilization. Raman spectroscopy revealed the dispersion of the immobilized MP8 molecules in MIL-101­(Cr)-X matrices as monomers without aggregation. The presence of functional groups resulted in higher amounts of immobilized MP8 in comparison to the bare MIL-101­(Cr). The catalytic activity of MP8@MIL-101­(Cr)-NH2 per material mass was higher than that for MP8@MIL-101­(Cr). The presence of free amino groups can thus improve the immobilization efficiency, leading to a higher amount of catalytically active species and improving the subsequent catalytic activity of the heterogeneous biocatalysts. MP8@MIL­(Cr)-X also successfully catalyzed the selective oxidation of thioanisole derivatives into sulfoxides.
ISSN:2574-0970
2574-0970
DOI:10.1021/acsanm.9b02464