The Laccase‐Lig Multienzymatic Multistep System in Lignin Valorization. Issue 20 (2nd September 2022)
- Record Type:
- Journal Article
- Title:
- The Laccase‐Lig Multienzymatic Multistep System in Lignin Valorization. Issue 20 (2nd September 2022)
- Main Title:
- The Laccase‐Lig Multienzymatic Multistep System in Lignin Valorization
- Authors:
- Vignali, Elisa
Gigli, Matteo
Cailotto, Simone
Pollegioni, Loredano
Rosini, Elena
Crestini, Claudia - Abstract:
- Abstract: A laccase‐Lig multienzymatic multistep system for lignin depolymerization was designed and developed. Studies were performed on pristine and fractionated lignins (Kraft and Organosolv) using a specific cascade of enzymes, that is, laccases from Bacillus licheniformis and from Funalia trogii, respectively for Kraft and Organosolv lignin, followed by the Lig system from Sphingobium sp. SYK‐6 (β‐etherases Lig E and Lig F, glutathione lyase Lig G). Careful elucidation of the structural modifications occurring in the residual lignins associated with the identification and quantification of the generated low‐molecular‐weight compounds showed that (i) the laccase‐Lig system cleaves non‐phenolic aryl glycerol β‐O‐4 aryl ether bonds, and (ii) the overall reactivity is heavily dependent on the individual lignin structure. More specifically, samples with low phenolic/aliphatic OH groups ratio undergo net depolymerization, while an increased phenolic/aliphatic OH ratio results in the polymerization of the residual lignin irrespective of its botanical origin and isolation process. Abstract : Multistep catalysis : The ratio between phenolic and aliphatic OH groups plays a crucial role in determining the overall reactivity towards the cleavage of non‐phenolic aryl glycerol β‐O‐4 aryl ether bonds of lignin by the Laccase‐Lig multistep catalytic system. Lignin samples showing low phenolic/aliphatic OH ratio undergo net depolymerization, while a higher phenolic/aliphatic OH ratioAbstract: A laccase‐Lig multienzymatic multistep system for lignin depolymerization was designed and developed. Studies were performed on pristine and fractionated lignins (Kraft and Organosolv) using a specific cascade of enzymes, that is, laccases from Bacillus licheniformis and from Funalia trogii, respectively for Kraft and Organosolv lignin, followed by the Lig system from Sphingobium sp. SYK‐6 (β‐etherases Lig E and Lig F, glutathione lyase Lig G). Careful elucidation of the structural modifications occurring in the residual lignins associated with the identification and quantification of the generated low‐molecular‐weight compounds showed that (i) the laccase‐Lig system cleaves non‐phenolic aryl glycerol β‐O‐4 aryl ether bonds, and (ii) the overall reactivity is heavily dependent on the individual lignin structure. More specifically, samples with low phenolic/aliphatic OH groups ratio undergo net depolymerization, while an increased phenolic/aliphatic OH ratio results in the polymerization of the residual lignin irrespective of its botanical origin and isolation process. Abstract : Multistep catalysis : The ratio between phenolic and aliphatic OH groups plays a crucial role in determining the overall reactivity towards the cleavage of non‐phenolic aryl glycerol β‐O‐4 aryl ether bonds of lignin by the Laccase‐Lig multistep catalytic system. Lignin samples showing low phenolic/aliphatic OH ratio undergo net depolymerization, while a higher phenolic/aliphatic OH ratio results in the polymerization of the residual lignin irrespective of its origin. … (more)
- Is Part Of:
- ChemSusChem. Volume 15:Issue 20(2022)
- Journal:
- ChemSusChem
- Issue:
- Volume 15:Issue 20(2022)
- Issue Display:
- Volume 15, Issue 20 (2022)
- Year:
- 2022
- Volume:
- 15
- Issue:
- 20
- Issue Sort Value:
- 2022-0015-0020-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-09-02
- Subjects:
- biomass conversion -- laccase -- lignin -- ligninolytic enzymes -- recombinant enzymes
Green chemistry -- Periodicals
Sustainable engineering -- Periodicals
Chemistry -- Periodicals
Chemical engineering -- Periodicals
660 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291864-564X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cssc.202201147 ↗
- Languages:
- English
- ISSNs:
- 1864-5631
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3133.482500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24153.xml