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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...

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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
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author Ni, Yun
Lv, Zhixiang
Wang, Zhou
Kang, Shouyu
He, Dawei
Liu, Ruijiang
author_facet Ni, Yun
Lv, Zhixiang
Wang, Zhou
Kang, Shouyu
He, Dawei
Liu, Ruijiang
author_sort Ni, Yun
collection PubMed
description 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.
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spelling pubmed-88318382022-02-12 Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets Ni, Yun Lv, Zhixiang Wang, Zhou Kang, Shouyu He, Dawei Liu, Ruijiang Front Bioeng Biotechnol Bioengineering and Biotechnology 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. Frontiers Media S.A. 2022-01-28 /pmc/articles/PMC8831838/ /pubmed/35155412 http://dx.doi.org/10.3389/fbioe.2021.812403 Text en Copyright © 2022 Ni, Lv, Wang, Kang, He and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Ni, Yun
Lv, Zhixiang
Wang, Zhou
Kang, Shouyu
He, Dawei
Liu, Ruijiang
Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets
title Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets
title_full Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets
title_fullStr Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets
title_full_unstemmed Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets
title_short Immobilization and Evaluation of Penicillin G Acylase on Hydroxy and Aldehyde Functionalized Magnetic α-Fe(2)O(3)/Fe(3)O(4) Heterostructure Nanosheets
title_sort immobilization and evaluation of penicillin g acylase on hydroxy and aldehyde functionalized magnetic α-fe(2)o(3)/fe(3)o(4) heterostructure nanosheets
topic Bioengineering and Biotechnology
url 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
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