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dc.date.accessioned2023-08-11T17:03:00Z
dc.date.available2023-08-11T17:03:00Z
dc.date.created2023-03-15T15:42:48Z
dc.date.issued2023
dc.identifier.citationKommedal, Eirik Angeltveit, Camilla Fløien Klau, Leesa Jane Ayuso-Fernandez, Ivan Arstad, Bjørnar Antonsen, Simen Stenstrøm, Yngve Ekeberg, Dag Gírio, Francisco Carvalheiro, Florbela Horn, Svein Jarle Aachmann, Finn Lillelund Eijsink, Vincent . Visible light-exposed lignin facilitates cellulose solubilization by lytic polysaccharide monooxygenases. Nature Communications. 2023, 14(1)
dc.identifier.urihttp://hdl.handle.net/10852/103176
dc.description.abstractAbstract Lytic polysaccharide monooxygenases (LPMOs) catalyze oxidative cleavage of crystalline polysaccharides such as cellulose and are crucial for the conversion of plant biomass in Nature and in industrial applications. Sunlight promotes microbial conversion of plant litter; this effect has been attributed to photochemical degradation of lignin, a major redox-active component of secondary plant cell walls that limits enzyme access to the cell wall carbohydrates. Here, we show that exposing lignin to visible light facilitates cellulose solubilization by promoting formation of H 2 O 2 that fuels LPMO catalysis. Light-driven H 2 O 2 formation is accompanied by oxidation of ring-conjugated olefins in the lignin, while LPMO-catalyzed oxidation of phenolic hydroxyls leads to the required priming reduction of the enzyme. The discovery that light-driven abiotic reactions in Nature can fuel H 2 O 2 -dependent redox enzymes involved in deconstructing lignocellulose may offer opportunities for bioprocessing and provides an enzymatic explanation for the known effect of visible light on biomass conversion.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleVisible light-exposed lignin facilitates cellulose solubilization by lytic polysaccharide monooxygenases
dc.title.alternativeENEngelskEnglishVisible light-exposed lignin facilitates cellulose solubilization by lytic polysaccharide monooxygenases
dc.typeJournal article
dc.creator.authorKommedal, Eirik
dc.creator.authorAngeltveit, Camilla Fløien
dc.creator.authorKlau, Leesa Jane
dc.creator.authorAyuso-Fernandez, Ivan
dc.creator.authorArstad, Bjørnar
dc.creator.authorAntonsen, Simen
dc.creator.authorStenstrøm, Yngve
dc.creator.authorEkeberg, Dag
dc.creator.authorGírio, Francisco
dc.creator.authorCarvalheiro, Florbela
dc.creator.authorHorn, Svein Jarle
dc.creator.authorAachmann, Finn Lillelund
dc.creator.authorEijsink, Vincent
cristin.unitcode185,15,23,30
cristin.unitnameSeksjon for farmakologi og farmasøytisk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2134206
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Nature Communications&rft.volume=14&rft.spage=&rft.date=2023
dc.identifier.jtitleNature Communications
dc.identifier.volume14
dc.identifier.issue1
dc.identifier.doihttps://doi.org/10.1038/s41467-023-36660-4
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2041-1723
dc.type.versionPublishedVersion
cristin.articleid1063
dc.relation.projectNFR/269408
dc.relation.projectNFR/268002
dc.relation.projectEC/HEU/ERC-856446
dc.relation.projectNFR/315385
dc.relation.projectNFR/262853
dc.relation.projectNFR/257622


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