Functional screening pipeline to uncover laccase-like multicopper oxidase enzymes that transform industrial lignins

dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorSharan, Anupama A.en_US
dc.contributor.authorBellemare, Annieen_US
dc.contributor.authorDiFalco, Marcosen_US
dc.contributor.authorTsang, Adrianen_US
dc.contributor.authorVuong, Thu V.en_US
dc.contributor.authorEdwards, Elizabeth A.en_US
dc.contributor.authorMaster, Emma R.en_US
dc.contributor.departmentDepartment of Bioproducts and Biosystemsen
dc.contributor.groupauthorProtein Technologyen
dc.contributor.organizationUniversity of Torontoen_US
dc.contributor.organizationConcordia Universityen_US
dc.date.accessioned2024-01-04T08:50:12Z
dc.date.available2024-01-04T08:50:12Z
dc.date.issued2024-02en_US
dc.descriptionFunding Information: The authors would like to acknowledge Mathieu Lavallee from Concordia University for support with heterologous production of multicopper oxidase enzymes presented in the study and Matthew Mascioni from the University of Toronto for development of R scripts used in ToF-SIMS data analysis. This work was supported by Genome Canada for the LSARP project “SYNBIOMICS – Functional genomics and techno-economic models for advanced biopolymer synthesis” (grant number 10405) and the NSERC CREATE for BioZone (grant number 528163). Publisher Copyright: © 2023
dc.description.abstractLaccase-like multicopper oxidases are recognized for their potential to alter the reactivity of lignins for application in value-added products. Typically, model compounds are employed to discover such enzymes; however, they do not represent the complexity of industrial lignin substrates. In this work, a screening pipeline was developed to test enzymes simultaneously on model compounds and industrial lignins. A total of 12 lignin-active fungal multicopper oxidases were discovered, including 9 enzymes active under alkaline conditions (pH 11.0). Principal component analysis revealed the poor ability of model compounds to predict enzyme performance on industrial lignins. Additionally, sequence similarity analyses grouped these enzymes with Auxiliary Activity-1 sub-families with few previously characterized members, underscoring their taxonomic novelty. Correlation between the lignin-activity of these enzymes and their taxonomic origin, however, was not observed. These are critical insights to bridge the gap between enzyme discovery and application for industrial lignin valorization.en
dc.description.versionPeer revieweden
dc.format.extent10
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationSharan, A A, Bellemare, A, DiFalco, M, Tsang, A, Vuong, T V, Edwards, E A & Master, E R 2024, ' Functional screening pipeline to uncover laccase-like multicopper oxidase enzymes that transform industrial lignins ', Bioresource Technology, vol. 393, 130084 . https://doi.org/10.1016/j.biortech.2023.130084en
dc.identifier.doi10.1016/j.biortech.2023.130084en_US
dc.identifier.issn0960-8524
dc.identifier.issn1873-2976
dc.identifier.otherPURE UUID: 4040cf13-cf8d-44e5-a53e-75b02f99cf34en_US
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/4040cf13-cf8d-44e5-a53e-75b02f99cf34en_US
dc.identifier.otherPURE LINK: http://www.scopus.com/inward/record.url?scp=85178102479&partnerID=8YFLogxK
dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/131011845/CHEM_Sharan_et_al_Functional_Screening_2023_Bioresource_Technology.pdfen_US
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/125397
dc.identifier.urnURN:NBN:fi:aalto-202401041086
dc.language.isoenen
dc.publisherElsevier
dc.relation.ispartofseriesBioresource Technologyen
dc.relation.ispartofseriesVolume 393en
dc.rightsopenAccessen
dc.subject.keywordKraft ligninen_US
dc.subject.keywordLaccaseen_US
dc.subject.keywordLignin-active enzymesen_US
dc.subject.keywordOrganosolv ligninen_US
dc.subject.keywordToF-SIMSen_US
dc.titleFunctional screening pipeline to uncover laccase-like multicopper oxidase enzymes that transform industrial ligninsen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi
dc.type.versionpublishedVersion

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