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A novel automatable enzyme-coupled colorimetric assay for endo-1,4-β-glucanase (cellulase).

Authors :
Mangan D
Cornaggia C
McKie V
Kargelis T
McCleary BV
Source :
Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2016 Jun; Vol. 408 (15), pp. 4159-68. Date of Electronic Publication: 2016 Apr 06.
Publication Year :
2016

Abstract

endo-1,4-β-Glucanase (endo-cellulase, EC 3.2.1.4) is one of the most widely used enzymes in industry. Despite its importance, improved methods for the rapid, selective, quantitative assay of this enzyme have been slow to emerge. In 2014, a novel enzyme-coupled assay that addressed many of the limitations of the existing assay methodology was reported. This involved the use of a bifunctional substrate chemically derived from cellotriose. Reported herein is a much improved version of this assay employing a novel substrate, namely 4,6-O-(3-ketobutylidene)-4-nitrophenyl-β-D-cellopentaoside. Graphical Abstract Principle of the CELLG5 assay.

Details

Language :
English
ISSN :
1618-2650
Volume :
408
Issue :
15
Database :
MEDLINE
Journal :
Analytical and bioanalytical chemistry
Publication Type :
Academic Journal
Accession number :
27052773
Full Text :
https://doi.org/10.1007/s00216-016-9507-y