2'-Deoxyribosyltransferase from Leishmania mexicana, an efficient biocatalyst for one-pot, one-step synthesis of nucleosides from poorly soluble purine bases

dc.contributor.authorCrespo, Noé
dc.contributor.authorSánchez Murcia, Pedro Alejandro
dc.contributor.authorGago, Federico
dc.contributor.authorCejudo Sanches, Janaina
dc.contributor.authorGalmes, Miguel Angel
dc.contributor.authorFernández Lucas, Jesús
dc.contributor.authorMancheño, José Miguel
dc.date.accessioned2017-09-04T09:47:18Z
dc.date.available2017-09-04T09:47:18Z
dc.date.issued2017
dc.description.abstractProcesses catalyzed by enzymes offer numerous advantages over chemical methods although in many occasions the stability of the biocatalysts becomes a serious concern. Traditionally, synthesis of nucleosides using poorly water-soluble purine bases, such as guanine, xanthine, or hypoxanthine, requires alkaline pH and/or high temperatures in order to solubilize the substrate. In this work, we demonstrate that the 2′-deoxyribosyltransferase from Leishmania mexicana (LmPDT) exhibits an unusually high activity and stability under alkaline conditions (pH 8–10) across a broad range of temperatures (30–70 °C) and ionic strengths (0–500 mM NaCl). Conversely, analysis of the crystal structure of LmPDT together with comparisons with hexameric, bacterial homologues revealed the importance of the relationships between the oligomeric state and the active site architecture within this family of enzymes. Moreover, molecular dynamics and docking approaches provided structural insights into the substrate-binding mode. Biochemical characterization of LmPDT identifies the enzyme as a type I NDT (PDT), exhibiting excellent activity, with specific activity values 100- and 4000-fold higher than the ones reported for other PDTs. Interestingly, LmPDT remained stable during 36 h at different pH values at 40 °C. In order to explore the potential of LmPDT as an industrial biocatalyst, enzymatic production of several natural and non-natural therapeutic nucleosides, such as vidarabine (ara A), didanosine (ddI), ddG, or 2′-fluoro-2′-deoxyguanosine, was carried out using poorly water-soluble purines. Noteworthy, this is the first time that the enzymatic synthesis of 2′-fluoro-2′-deoxyguanosine, ara G, and ara H by a 2′-deoxyribosyltransferase is reported 2'-Deoxyribosyltransferase from Leishmania mexicana, an efficient biocatalyst for one-pot, one-step synthesis of nucleosides from poorly soluble purine bases.spa
dc.description.filiationUEMspa
dc.description.impact3.340 JCR (2017) Q2, 46/160 Biotechnology and Applied Microbiologyspa
dc.description.sponsorshipFundación Santander, Universidad Europeaspa
dc.identifier.citationCrespo, N., Sánchez-Murcia, P. A., Gago, F., Cejudo-Sanches, J., Galmes, M. A., Fernández-Lucas, J., & Mancheño, J. M. (2017). 2′-Deoxyribosyltransferase from Leishmania mexicana, an efficient biocatalyst for one-pot, one-step synthesis of nucleosides from poorly soluble purine bases. Applied Microbiology and Biotechnology,101(19), 7187-7200.spa
dc.identifier.doi10.1007/s00253-017-8450-y
dc.identifier.issn01757598
dc.identifier.urihttp://hdl.handle.net/11268/6579
dc.language.isoengspa
dc.peerreviewedSispa
dc.rights.accessRightsrestricted accessspa
dc.subject.uemEnzimasspa
dc.subject.uemLeishmaniosisspa
dc.subject.unescoEnzimaspa
dc.subject.unescoProteínaspa
dc.title2'-Deoxyribosyltransferase from Leishmania mexicana, an efficient biocatalyst for one-pot, one-step synthesis of nucleosides from poorly soluble purine basesspa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublication65bdb4fa-7adf-42ce-b40e-421a62e05239
relation.isAuthorOfPublication.latestForDiscovery65bdb4fa-7adf-42ce-b40e-421a62e05239

Files