Abstract

High costs and low production efficiency are a serious constraint to bio-based xylitol production. For industrial-scale production of xylitol, a plasmid-free Escherichia coli for arabitol-free xylitol production from corncob hemicellulosic hydrolysate has been constructed. Instead of being plasmid and inducer dependent, this strain relied on multiple-copy integration of xylose reductase (XR) genes into the chromosome, where their expression was controlled by the constitutive promoter P43. In addition, to minimize the flux from L-arabinose to arabitol, two strategies including low XR total activity and high selectivity of XR has been adopted. Arabitol was significantly decreased using plasmid-free strain which had lower XR total activity and an eight point-mutations of XR with a 27-fold lower enzyme activity toward L-arabinose was achieved. The plasmid-free strain in conjunction with this mutant XR can completely eliminate arabitol formation in xylitol production. In fed-batch fermentation, this plasmid-free strain produced 143.8 g L−1 xylitol at 1.84 g L−1 h−1 from corncob hemicellulosic hydrolysate. From these results, we conclude that this route by plasmid-free E. coli has potential to become a commercially viable process for xylitol production.

Highlights

  • High costs and low production efficiency are a serious constraint to bio-based xylitol production

  • For industrial-scale production of xylitol, a plasmid-free Escherichia coli for arabitol-free xylitol production from corncob hemicellulosic hydrolysate has been constructed

  • Instead of being plasmid and inducer dependent, this strain relied on multiple-copy integration of xylose reductase (XR) genes into the chromosome, where their expression was controlled by the constitutive promoter P43

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Summary

Introduction

High costs and low production efficiency are a serious constraint to bio-based xylitol production. For industrial-scale production of xylitol, a plasmid-free Escherichia coli for arabitol-free xylitol production from corncob hemicellulosic hydrolysate has been constructed. In fed-batch fermentation, this plasmidfree strain produced 143.8 g L−1 xylitol at 1.84 g L−1 h−1 from corncob hemicellulosic hydrolysate From these results, we conclude that this route by plasmid-free E. coli has potential to become a commercially viable process for xylitol production. We used plasmid-based VMCQI in E. coli, almost all the L-arabinose in the corncob hemicellulosic hydrolysate has been reduced to L-arabitol in 5L-scale fermentation[2]. To engineer E. coli for more economical production of arabitol-free xylitol from corncob hemicellulosic hydrolysate, the aim of this study is to perform multi-copy chromosomal integration of N. crassa XR genes controlled by constitutive promoter in order to achieve stable xylitol production. The synergy manifested as increased selectivity such that L-arabitol formation was completely eliminated in xylitol production from corncob hemicellulosic hydrolysate

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