Immobilization of carbonic anhydrase on polyethylenimine/dopamine codeposited membranes
ABSTRACT Carbonic anhydrase (CA) catalyzing CO2 hydration has an important application in carbon capture, and its immobilization is very significant. Here, CA was covalently linked by glutaraldehyde (GA) to the surface of poly(vinylidene fluoride) (PVDF) and polyethylene (PE) membranes, which were p...
Gespeichert in:
Veröffentlicht in: | Journal of applied polymer science 2019-08, Vol.136 (29), p.n/a |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | ABSTRACT
Carbonic anhydrase (CA) catalyzing CO2 hydration has an important application in carbon capture, and its immobilization is very significant. Here, CA was covalently linked by glutaraldehyde (GA) to the surface of poly(vinylidene fluoride) (PVDF) and polyethylene (PE) membranes, which were previously modified via a simple codeposition of polyethyleneimine (PEI) and dopamine (DA). The effects of the modification conditions were investigated, and the membranes were characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The immobilization process was optimized, and the catalytic properties of immobilized CA were studied. The results show that the optimal mass ratio of PEI and DA was 1:1 and the deposition time was 10–12 h, at which the surface amino group density could reach 1.278 × 10−7 and 1.397 × 10−7 mol/cm2 for PVDF and PE, respectively. For enzyme immobilization, the optimal CA and GA concentrations were 0.2 mg/mL and 0.1 wt %, and a maximum activity recovery of about 53% and 76% could be achieved for PVDF‐attached CA and PE‐attached CA, respectively. Their Km values were 10.62 mM and 8.6 mM, and the corresponding Kcat/Km values were 132.2 M−1 s−1 and 312.9 M−1 s−1. After immobilization, the storage stability and reusability of CA were much improved. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47784. |
---|---|
ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.47784 |