Abstract

Various types of lignocellulosic wastes extensively used in biofuel production were provided to assess the potential of EXLX1 as a cellulase synergist. Enzymatic hydrolysis of natural wheat straw showed that all the treatments using mixtures of cellulase and an optimized amount of EXLX1, released greater quantities of sugars than those using cellulase alone, regardless of cellulase dosage and incubation time. EXLX1 exhibited different synergism and binding characteristics for different wastes, but this can be related to their lignocellulosic components. The cellulose proportion could be one of the important factors. However, when the cellulose proportion of different biomass samples exhibited no remarkable differences, a higher synergism of EXLX1 is prone to occur on these materials, with a high proportion of hemicellulose and a low proportion of lignin. The information could be favorable to assess whether EXLX1 is effective as a cellulase synergist for the hydrolysis of the used materials. Binding assay experiments further suggested that EXLX1 bound preferentially to alkali pretreated materials, as opposed to acid pretreated materials under the assay condition and the binding preference would be affected by incubation temperature.

Highlights

  • Lignocellulosic waste is a promising resource for producing fuels and chemicals, both natural and man-made [1]

  • EXLX1 was purified using a 6-His tag located at the carboxyl-terminus of the protein (Fig.1a) and approximately 35 mg of purified EXLX1 was obtained from 1 L of culture broth

  • Determination of the synergistic activity of the purified EXLX1 with cellulase was performed with bovine serum albumin (BSA) used instead of EXLX1 in the negative control experiments

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Summary

Introduction

Lignocellulosic waste is a promising resource for producing fuels and chemicals, both natural and man-made [1]. As the most abundant and renewable source on earth, lignocellulose consists of three major components: cellulose, hemicellulose and lignin [2]. Deconstruction of lignocellulose into fermentable sugars is a key process in its conversion to high-value chemicals and an array of glycoside hydrolases is required. Design of glycoside hydrolase mixtures that function synergistically to release sugars from biomass has been known to be an effective strategy [3,4]. Combined utilization of proteins lacking glycoside hydrolase activity (non-GH) with glycoside hydrolases such as cellulase has been suggested as another effective option to facilitate the release of sugars from lignocellulosic biomass [5,6]

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