Abstract

A glucoamylase-immobilized system based on cross-linked gelatin nanoparticles (CLGNs) was prepared by coacervation method. This system exhibited characteristics of temperature-triggered phase transition, which could be used for enzyme immobilization and release. Their morphology and size distribution were examined by transmission electron microscopy and dynamic light scattering particle size analyzer. Their temperature-triggered glucoamylase immobilization and release features were also further investigated under different temperatures. Results showed that the CLGNs were regularly spherical with diameters of 155±5 nm. The loading efficiencies of glucoamylase immobilized by entrapment and adsorption methods were 59.9% and 24.7%, respectively. The immobilized enzyme was released when the system temperature was above 40°C and performed high activity similar to free enzyme due to the optimum temperature range for glucoamylase. On the other hand, there was no enzyme release that could be found when the system temperature was below 40°C. The efficiency of temperature-triggered release was as high as 99.3% for adsorption method, while the release of enzyme from the entrapment method was not detected. These results indicate that CLGNs are promising matrix for temperature-triggered glucoamylase immobilization and release by adsorption immobilization method.

Highlights

  • Enzyme immobilization is a technique in which an enzyme is made to attach to an inert material

  • The time taken for the phase transition of cross-linked gelatin nanoparticles (CLGNs) was recorded as response time

  • The results showed that at room temperature, CLGNs were monodispersed with diameter of 15565 nm and polydispersity index (PdI) around 0.14

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Summary

Introduction

Enzyme immobilization is a technique in which an enzyme is made to attach to an inert material. The glucoamylase adsorbed CLGNs solution was stored at 4uC prior the measurement of temperature-triggered release of enzyme. The acetate anion modified CLGNs showed a quicker response time, 1.0 mL of 2.0 mol/L sodium acetate was used as the modification solution in the preparation of reversible temperature-sensitive CLGNs. Morphology and Size Distribution of Cross-linked Gelatin

Results
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