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Updated: May 6, 2026

High-throughput Saccharification Assay for Lignocellulosic Materials
Published on: July 3, 2011
Assessment of the enzymatic hydrolysis profile of cellulosic substrates based on reducing sugar release
Marcos Henrique Luciano Silveira1, Rodrigo Souza Aguiar, Matti Siika-aho
1Research Center in Applied Chemistry (CEPESQ), Department of Chemistry, Federal University of Paraná, P.O. Box 19081, Curitiba, Paraná 81531-970, Brazil; VTT Technical Research Centre of Finland, P.O. Box 1000, 02044 VTT Espoo, Finland.
Abstract:
The activity profile of a 1:0.30 mixture of Celluclast 1.5L FG and Novozym 188 (Novozymes) was investigated using Whatman #1 filter paper (W1FP) as a single substrate for hydrolysis. The procedure was based on the ability of the enzymes to release total (RS(Tot)), insoluble (RS(Insol)) and soluble (RS(Sol)) reducing sugars from W1FP. RS(Insol) was used to estimate endoglucanase (EnG) activity whereas exoglucanases (ExG) were assessed by measuring RSSol in the presence of δ-gluconolactone. Finally, the β-glucosidase (βG) activity was derived from the difference between RS(Sol) measurements in the presence and absence of δ-gluconolactone. When this analytical procedure was applied to W1FP using 9.64 mg mL(-1) of the enzyme mixture, the relative contributions of EnG, ExG and βG to the total cellulase activity were 63.28%, 12.02% and 24.70%, respectively. Also, this ratio changed with changes in the enzyme loading, giving a new insight into the synergy that exists among the enzymes.
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