Lignin depolymerization from softwood biomass using integrated protic ionic liquid–enzyme pretreatment

Sharib Khan, Daniel Rauber, Luyao Wang, Udayakumar Veerabagu, Christopher W. M. Kay, Chunlin Xu, Sabarathinam Shanmugam, Timo Kikas

Research output: Contribution to journalArticleScientificpeer-review

1 Citation (Scopus)

Abstract

Lignin, a vital component of plant biomass, offers significant potential for advanced biorefineries seeking to produce high-value chemicals and materials. However, maximizing lignin yield while ensuring its efficient valorization remains a substantial challenge in biorefineries. In this study, an integrated approach to producing lignin-derived oligomers and monomers was developed from softwood biomass. Pinus sylvestris was processed using a protic ionic liquid (PIL), triethylammonium methane sulfonate ([N222H][OMS]), to extract lignin, followed by its targeted depolymerization using bacterial laccases. Advanced analytical techniques were employed to investigate the qualitative and quantitative changes in lignin during the optimization and depolymerization stages. The findings highlight the effectiveness of [N222H][OMS] in removing 87.90% of lignin from pine wood at 180 °C. Furthermore, engineered bacterial laccases demonstrated significant catalytic activity, converting 9.2% of aliphatic hydroxyl groups and 73.8% of phenolic hydroxyl groups in lignin into carboxylic acids. Similarly, benchmarked against commercially available kraft lignin, the same depolymerization approach achieved lower conversion rates, transforming 12.4% aliphatic and 44.5% phenolic hydroxyl groups in lignin into carboxylic acids. Thus, this integrated strategy, combining ionic liquid delignification with enzymatic upgrading, presents a scalable and efficient route for maximizing lignin valorization.

Original languageEnglish
Pages (from-to)4466-4477
JournalRSC Sustainability
Volume3
Issue number10
DOIs
Publication statusPublished - 1 Oct 2025
MoE publication typeA1 Journal article-refereed

Funding

This work was supported by the Estonian Research Council Grant PRG2730 and the EEA Grant of Iceland, Liechtenstein, and Norway (Agreement No. EEZ/BPP/VIAA/2021/7). S. K. would like to acknowledge the Erasmus+ mobility grant “Co-funded by the Erasmus+ Programme of the European Union” and S. S. would also like to acknowledge the Short-Term Scientific Mission (STSM) grant funded by the COST Action (E-COST-GRANT-CA17128-6ca97f20). The authors would like to acknowledge the team at the NMR Service Center at Saaraland University for their support in instrumentation and technical assistance for NMR. They also thank Antoine Mialon (Neste), Petri Ihalainen (VTT), and Anu Suonpää (MetGen) for their valuable discussions about lignin depolymerization and MetGen Oy for sending commercially available and lab-engineered laccases as a gift.

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