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The Laccase-Lig Multienzymatic Multistep System in Lignin Valorization.
Vignali, Elisa; Gigli, Matteo; Cailotto, Simone; Pollegioni, Loredano; Rosini, Elena; Crestini, Claudia.
Afiliación
  • Vignali E; Department of Biotechnology and Life Sciences, University of Insubria, via J. H. Dunant 3, 21100, Varese, Italy.
  • Gigli M; Department of Molecular Sciences and Nanosystems, Ca'Foscari University of Venice, Via Torino 155, 30172, Venezia Mestre, Italy.
  • Cailotto S; CSGI/- Center for Colloid and Surface Science, Via della Lastruccia 3, 50019, Sesto Fiorentino, Italy.
  • Pollegioni L; Department of Molecular Sciences and Nanosystems, Ca'Foscari University of Venice, Via Torino 155, 30172, Venezia Mestre, Italy.
  • Rosini E; Department of Biotechnology and Life Sciences, University of Insubria, via J. H. Dunant 3, 21100, Varese, Italy.
  • Crestini C; Department of Biotechnology and Life Sciences, University of Insubria, via J. H. Dunant 3, 21100, Varese, Italy.
ChemSusChem ; 15(20): e202201147, 2022 Oct 21.
Article en En | MEDLINE | ID: mdl-35917230
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 (ß-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 ß-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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Lignina / Liasas Idioma: En Revista: ChemSusChem Asunto de la revista: QUIMICA / TOXICOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Lignina / Liasas Idioma: En Revista: ChemSusChem Asunto de la revista: QUIMICA / TOXICOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Italia