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Characterization of an atypical, thermostable, organic solvent- and acid-tolerant 2′-deoxyribosyltransferase from Chroococcidiopsis thermalis

dc.contributor.authorDel Arco, Jon
dc.contributor.authorSánchez-Murcia, Pedro Alejandro
dc.contributor.authorMancheño Gómez, José Miguel
dc.contributor.authorGago, Federico
dc.contributor.authorFernández Lucas, Jesús
dc.date.accessioned2024-11-04T16:41:35Z
dc.date.available2024-11-04T16:41:35Z
dc.date.issued2018
dc.description.abstractIn our search for thermophilic and acid-tolerant nucleoside 2′-deoxyribosyltransferases (NDTs), we found a good candidate in an enzyme encoded by Chroococcidiopsis thermalis PCC 7203 (CtNDT). Biophysical and biochemical characterization revealed CtNDT as a homotetramer endowed with good activity and stability at both high temperatures (50–100 °C) and a wide range of pH values (from 3 to 7). CtNDT recognizes purine bases and their corresponding 2′-deoxynucleosides but is also proficient using cytosine and 2′-deoxycytidine as substrates. These unusual features preclude the strict classification of CtNDT as either a type I or a type II NDT and further suggest that this simple subdivision may need to be updated in the future. Our findings also hint at a possible link between oligomeric state and NDT’s substrate specificity. Interestingly from a practical perspective, CtNDT displays high activity (80–100%) in the presence of several water-miscible co-solvents in a proportion of up to 20% and was successfully employed in the enzymatic production of several therapeutic nucleosides such as didanosine, vidarabine, and cytarabine.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (España)
dc.description.sponsorshipMinisterio de Ciencia e Innovación (España)
dc.description.sponsorshipUniversidad Europea de Madrid
dc.description.sponsorshipFundación Santander
dc.description.statuspub
dc.identifier.citationDel Arco, J., Sánchez-Murcia, P. A., Mancheño, J. M., Gago, F., & Fernández-Lucas, J. (2018). Characterization of an atypical, thermostable, organic solvent- and acid-tolerant 2′-deoxyribosyltransferase from Chroococcidiopsis thermalis. Applied Microbiology and Biotechnology, 102(16), 6947-6957. https://doi.org/10.1007/S00253-018-9134-Y
dc.identifier.doi10.1007/s00253-018-9134-y
dc.identifier.essn1432-0614
dc.identifier.issn0175-7598
dc.identifier.officialurlhttps://doi.org/10.1007/s00253-018-9134-y
dc.identifier.relatedurlhttps://link.springer.com/article/10.1007/s00253-018-9134-y
dc.identifier.urihttps://hdl.handle.net/20.500.14352/109960
dc.journal.titleApplied Microbiology and Biotechnology
dc.language.isoeng
dc.page.final6957
dc.page.initial6947
dc.publisherSpringer Nature
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2015-64629-C2-2-R/CARACTERIZACION Y BLOQUEO MEDIANTE PEPTIDOS Y MOLECULAS PEQUEÑAS DE PROTEINAS DIANA IMPLICADAS EN LA PROLIFERACION DE MICROORGANISMOS PATOGENOS Y CELUAS CANCEROSAS
dc.relation.projectIDinfo:eu-repo/grantAgreement/Universidad Europea de Madrid//2017%2FUEM23/ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/Fundación Santander//SAN151610/ES
dc.rights.accessRightsrestricted access
dc.subject.cdu577.15
dc.subject.cdu579.8
dc.subject.cdu579.22.08
dc.subject.keywordEnzymatic synthesis
dc.subject.keywordNucleoside analogues
dc.subject.keywordNucleoside 2′-deoxyribosyltransferase
dc.subject.keywordExtremophiles
dc.subject.keywordHomology modeling
dc.subject.ucmBioquímica (Biología)
dc.subject.ucmMicrobiología (Biología)
dc.subject.ucmBiotecnología
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2414 Microbiología
dc.subject.unesco2302.09 Enzimología
dc.subject.unesco2302.23 Ácidos Nucleicos
dc.titleCharacterization of an atypical, thermostable, organic solvent- and acid-tolerant 2′-deoxyribosyltransferase from Chroococcidiopsis thermalis
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number102
dspace.entity.typePublication
relation.isAuthorOfPublication90df27fb-817a-478c-9b45-61baa88a66bb
relation.isAuthorOfPublicationf99cf5b4-0f0d-424c-afd9-77bdedffd366
relation.isAuthorOfPublication.latestForDiscovery90df27fb-817a-478c-9b45-61baa88a66bb

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