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Updated: Mar 23, 2026

High Throughput Screening of Fungal Endoglucanase Activity in Escherichia coli
Published on: August 13, 2011
A novel automatable enzyme-coupled colorimetric assay for endo-1,4-β-glucanase (cellulase)
David Mangan1, Claudio Cornaggia2, Vincent McKie2
1Megazyme International Ireland, Bray Business Park, Southern Cross Road, Bray, County Wicklow, A98 YV29, Ireland. david@megazyme.com.
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.

