Cargando…

Fragmented α-Amylase into Microporous Metal-Organic Frameworks as Bioreactors

This work presents an efficient and facile strategy to prepare an α-amylase bioreactor. As enzymes are quite large to be immobilized inside metal-organic frameworks (MOFs), the tertiary and quaternary structures of α-amylase were first disrupted using a combination of urea, dithiothreitol (DTT), and...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Li-Hao, Chiu, Ru-Yin, So, Pamela Berilyn, Lirio, Stephen, Huang, Hsi-Ya, Liu, Wan-Ling, Lin, Chia-Her
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918099/
https://www.ncbi.nlm.nih.gov/pubmed/33670380
http://dx.doi.org/10.3390/ma14040870
Descripción
Sumario:This work presents an efficient and facile strategy to prepare an α-amylase bioreactor. As enzymes are quite large to be immobilized inside metal-organic frameworks (MOFs), the tertiary and quaternary structures of α-amylase were first disrupted using a combination of urea, dithiothreitol (DTT), and iodoacetamide (IAA). After losing its tertiary structure, the unfolded proteins can now penetrate into the microporous MOFs, affording fragmented α-amylase@MOF bioreactors. Among the different MOFs evaluated, UiO-66 gave the most promising potential due to the size-matching effect of the α-helix of the fragmented α-amylase with the pore size of UiO-66. The prepared bioreactor exhibited high yields of small carbohydrate (maltose) even when reused up to 15 times (>80% conversion).