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One-step immobilization-purification of enzymes by carbohydrate-binding module family 56 tag fusion.
- Source :
-
Food chemistry [Food Chem] 2019 Nov 30; Vol. 299, pp. 125037. Date of Electronic Publication: 2019 Jun 18. - Publication Year :
- 2019
-
Abstract
- Immobilization of enzymes is an essential strategy with outstanding prospects in biocatalytic processes. Nontoxic, inexpensive immobilized enzyme approach is especially important for food enzymes. We here demonstrate that a carbohydrate-binding module family 56 domain (CBM56-Tag) mediates the immobilization of fusion enzymes with the curdlan (β-1,3-glucan) particle support, thereby enabling the one-step immobilization-purification of target enzymes. CBM56-Tag exhibits an immunoglobulin-like β-sandwich fold, which can be adsorbed by curdlan via hydrogen bond-mediated binding. The maximum adsorption capacity of a fusion chitosanase (CBM56-GsCsn46A) on curdlan is 50.72 mg/g. The immobilized enzyme could be directly used in the packed-bed reactor. This immobilization strategy utilizes a natural polysaccharide without any treatment, avoiding the negative environmental effects. Moreover, the one step immobilization-purification simplifies the purification step, which reduces the use of chemicals. Our study provides a nontoxic and inexpensive immobilization strategy for the biocatalytic reaction in food industry.<br /> (Copyright © 2019 Elsevier Ltd. All rights reserved.)
- Subjects :
- Biocatalysis
Enzymes, Immobilized metabolism
Glycoside Hydrolases metabolism
Hydrogen Bonding
beta-Glucans chemistry
Enzymes, Immobilized chemistry
Enzymes, Immobilized isolation & purification
Glycoside Hydrolases chemistry
Glycoside Hydrolases isolation & purification
Receptors, Cell Surface metabolism
Recombinant Fusion Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-7072
- Volume :
- 299
- Database :
- MEDLINE
- Journal :
- Food chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 31279128
- Full Text :
- https://doi.org/10.1016/j.foodchem.2019.125037