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Research Article | Open Access

Cellulose saccharification to alleviate CCR of xylose for enhanced 1, 2, 4-butanetriol production

Shengji Li, Lisha Qin, Mengyue Ge, Yao Zuo, Mengyang Li, Sheng Xu, Xin Wang( ), Kequan Chen
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, Jiangsu, 211816, China
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Abstract

1,2,4-Butanetriol (BT) is a valuable polyol with applications in pharmaceuticals, materials, and military sectors. BT biosynthesis primarily uses xylose as substrate, with glucose supporting cell growth. However, glucose-mediated carbon catabolite repression (CCR) suppresses xylose assimilation, limiting BT production. This study aimed to investigate the impact of glucose on xylose-driven BT production in dual-carbon-source utilization and to develop a cellulose-based simultaneous saccharification and fermentation (SSF) strategy for enhanced glucose management, thereby alleviating CCR and improving BT yields. Heterologous BT biosynthesis pathways were introduced into Escherichia coli, with catabolic genes xylAB and yiaE/ycdW knocked out and xylose transporter xylE overexpressed, the BT synthesis pathway was constructed. Optimized fermentation conditions yielded 2.85 g/L BT. Next, the glucose-xylose ratio was optimized by adding xylose at early exponential phase, while low initial glucose with fed-batch feeding significantly reduced CCR, resulting in a BT titer of 3.59 g/L. To further alleviate CCR, an SSF strategy with continuous low-concentration glucose supply from cellulose was implemented, achieving 4.48 g/L BT. Finally, cellulose-xylan co-utilization strategy yielded 1.35 g/L BT. This study provides a reference for alleviating the CCR effect caused by the utilization of dual-carbon-source in biosynthesizing BT, and offers insights for producing BT from lignocellulose.

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Cite this article:
Li S, Qin L, Ge M, et al. Cellulose saccharification to alleviate CCR of xylose for enhanced 1, 2, 4-butanetriol production. BioDesign Research, 2026, 8(3). https://doi.org/10.1016/j.bidere.2026.100103

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Received: 07 April 2026
Revised: 06 June 2026
Accepted: 23 June 2026
Published: 08 July 2026
© 2026 The Authors.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).