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Genome mining and characterisation of a novel transaminase with remote stereoselectivity

dc.contributor.authorGavin, Declan
dc.contributor.authorReen, Jerry
dc.contributor.authorRocha Martín, Javier
dc.contributor.authorAbreu-Castilla, Ignacio
dc.contributor.authorWoods, David
dc.contributor.authorFoley, Aoife
dc.contributor.authorSánchez-Murcia, Pedro
dc.contributor.authorSchwarz, Maria
dc.contributor.authorO’Neill, Pat
dc.contributor.authorMaguire, Anita
dc.contributor.authorO’Gara, Fergal
dc.date.accessioned2024-01-19T15:23:08Z
dc.date.available2024-01-19T15:23:08Z
dc.date.issued2019
dc.descriptionFunding Esta investigación fue financiada en parte por financiación de Enterprise Ireland (CF-2017-0757-P; IP-2015-0390), el Health Research Board (HRB-ILP-POR-2019-004), el Health Research Board/Irish Thoracic Sociedad (MRCG-2018-16; MRCG-2014-6), Comisión Europea (EU2020-634486-2015), Science Foundation Ireland (SSPC-3, 12/RC/2275_2; SSPC-2, 12/RC/2275; 15/TIDA/2977; SFI09/RFP/BMT2350), el Consejo Irlandés de Investigación en Ciencia, Ingeniería y Tecnología (GOIPG/2014/647), Fundación de Fibrosis Quística, EE. UU. (OG1710). PAS-M. agradece al FWF austriaco (Proyecto M 2260) por su apoyo financiero.
dc.description.abstractMicrobial enzymes from pristine niches can potentially deliver disruptive opportunities in synthetic routes to Active Pharmaceutical Ingredients and intermediates in the Pharmaceutical Industry. Advances in green chemistry technologies and the importance of stereochemical control, further underscores the application of enzyme-based solutions in chemical synthesis. The rich tapestry of microbial diversity in the oceanic ecosystem encodes a capacity for novel biotransformations arising from the chemical complexity of this largely unexplored bioactive reservoir. Here we report a novel ω-transaminase discovered in a marine sponge Pseudovibrio sp. isolate. Remote stereoselection using a transaminase has been demonstrated for the first time using this novel protein. Application to the resolution of an intermediate in the synthesis of sertraline highlights the synthetic potential of this novel biocatalyst discovered through genomic mining. Integrated chemico-genomics revealed a unique substrate profile, while molecular modelling provided structural insights into this ‘first in class’ selectivity at a remote chiral centre.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipEnterprise Ireland
dc.description.sponsorshipHealth Research Board (Ireland)
dc.description.sponsorshipIrish Toracic Society
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipScience Foundation Ireland
dc.description.sponsorshipIrish Research Council for Science, Engineering and Technology
dc.description.sponsorshipCystic Fibrosis Foundation (USA)
dc.description.sponsorshipAustrian Science Fund
dc.description.statuspub
dc.identifier.citationGavin, D.P., Reen, F.J., Rocha-Martin, J. et al. Genome mining and characterisation of a novel transaminase with remote stereoselectivity. Sci Rep 9, 20285 (2019). https://doi.org/10.1038/s41598-019-56612-7
dc.identifier.doi10.1038/s41598-019-56612-7
dc.identifier.issn2045-2322
dc.identifier.officialurlhttps://doi.org/10.1038/s41598-019-56612-7
dc.identifier.urihttps://hdl.handle.net/20.500.14352/94110
dc.journal.titleScientific Reports
dc.language.isoeng
dc.page.initial20285
dc.publisherSpringer Nature
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu577.1
dc.subject.cdu577.2
dc.subject.ucmBioquímica (Química)
dc.subject.ucmBiología molecular (Química)
dc.subject.unesco2302 Bioquímica
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2415 Biología Molecular
dc.titleGenome mining and characterisation of a novel transaminase with remote stereoselectivity
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number9
dspace.entity.typePublication
relation.isAuthorOfPublication9d7ac6de-a596-4647-a7fa-3a1c143055e4
relation.isAuthorOfPublication.latestForDiscovery9d7ac6de-a596-4647-a7fa-3a1c143055e4

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