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

Anal Bioanal Chem. 2016 Jun;408(15):4159-68. doi: 10.1007/s00216-016-9507-y. Epub 2016 Apr 6.

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.

Keywords: Assay; Automation; CELLG5; Cellulase; Colorimetric; endo-1,4-β-Glucanase.

Publication types

  • Evaluation Study

MeSH terms

  • Automation / methods*
  • Cellulase / analysis*
  • Colorimetry / methods*
  • Enzyme Assays / methods*

Substances

  • Cellulase