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Constructing Biopolymer-Inorganic Nanocomposite through a Biomimetic Mineralization Process for Enzyme Immobilization

Inspired by biosilicification, biomimetic polymer-silica nanocomposite has aroused a lot of interest from the viewpoints of both scientific research and technological applications. In this study, a novel dual functional polymer, NH(2)-Alginate, is synthesized through an oxidation-amination-reduction...

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Detalles Bibliográficos
Autores principales: Li, Jian, Ma, Jun, Jiang, Tao, Wang, Yanhuan, Wen, Xuemei, Li, Guozhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512666/
https://www.ncbi.nlm.nih.gov/pubmed/28793547
http://dx.doi.org/10.3390/ma8095286
Descripción
Sumario:Inspired by biosilicification, biomimetic polymer-silica nanocomposite has aroused a lot of interest from the viewpoints of both scientific research and technological applications. In this study, a novel dual functional polymer, NH(2)-Alginate, is synthesized through an oxidation-amination-reduction process. The “catalysis function” ensures the as-prepared NH(2)-Alginate inducing biomimetic mineralization of silica from low concentration precursor (Na(2)SiO(3)), and the “template function” cause microscopic phase separation in aqueous solution. The diameter of resultant NH(2)-Alginate micelles in aqueous solution distributed from 100 nm to 1.5 μm, and is influenced by the synthetic process of NH(2)-Alginate. The size and morphology of obtained NH(2)-Alginate/silica nanocomposite are correlated with the micelles. NH(2)-Alginate/silica nanocomposite was subsequently utilized to immobilize β-Glucuronidase (GUS). The harsh condition tolerance and long-term storage stability of the immobilized GUS are notably improved due to the buffering effect of NH(2)-Alginate and cage effect of silica matrix.