Cargando…

Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets

Magnetic α-Fe(2)O(3)/Fe(3)O(4) heterostructure nanosheets were fabricated via hydrothermal calcination. The activity of penicillin G acylase (PGA), which was covalently immobilized onto silica-decorated heterostructure nanosheets, achieved the highest activity of 387.03 IU/g after 18 h of incubation...

Descripción completa

Detalles Bibliográficos
Autores principales: Ni, Yun, Lv, Zhixiang, Wang, Zhou, Kang, Shouyu, He, Dawei, Liu, Ruijiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831838/
https://www.ncbi.nlm.nih.gov/pubmed/35155412
http://dx.doi.org/10.3389/fbioe.2021.812403
Descripción
Sumario:Magnetic α-Fe(2)O(3)/Fe(3)O(4) heterostructure nanosheets were fabricated via hydrothermal calcination. The activity of penicillin G acylase (PGA), which was covalently immobilized onto silica-decorated heterostructure nanosheets, achieved the highest activity of 387.03 IU/g after 18 h of incubation with 0.1 ml of PGA. In contrast, the activity of free PGA reached the highest level when the temperature was 45°C with a pH of 8.0. However, the activity of free PGA changed more dramatically than immobilized PGA as the relative conditions changed. Moreover, the Michaelis–Menten constant (K(m)) and reusability of immobilized PGA were also explored. The results showed that free PGA K(m) and maximum rate (V(max)) were 0.0274 M and 1.167 μl/min, respectively. K(m) and V(max) values of immobilized PGA were 0.1082 M and 1.294 μl/min, respectively. After 12 cycles of repetitive use, immobilized PGA remained approximately 66% of its initial activity, indicating that the PGA immobilized onto the heterostructure nanosheets showed better stability and reusability than free PGA.