Purine and pyrimidine phosphoribosyltransferases: A versatile tool for enzymatic synthesis of nucleoside-5′-monophosphates

dc.contributor.authorDel Arco, Jon
dc.contributor.authorFernández Lucas, Jesús
dc.date.accessioned2024-11-20T09:04:34Z
dc.date.available2024-11-20T09:04:34Z
dc.date.issued2017
dc.description.abstractBackground: In recent years, enzymatic methods have shown to be an efficient and sustainable alternative for the synthesis of nucleosides and nucleoside-5'-monophosphates (NMPs) to the traditional multistep chemical methods, since chemical glycosylation reactions include several protection–deprotection steps and the use of chemical reagents and organic solvents that are expensive and environmentally harmful. Results: In this mini-review, we want to illustrate the application of phosphoribosyltransferases (PRTs) in enzymatic synthesis of NMPs. In this sense, many different examples about the use of PRTs as biocatalysts, as whole cells or enzymes, are described. In addition, it also includes detailed comments about structure and catalytic mechanism of described PRTs, as well as their possible biological role and therapeutic use, substrate specificity and advances in detection of new enzyme specificities towards different substrates. In addition, several examples about the use of PRTs in mono or multi-enzymatic synthesis of NMP analogues are shown. Finally, a brief discussion about advantages and drawbacks of the use of PRTs as industrial biocatalyst of NMPs has been commented. Conclusion: Despite the great potential of PRTs as biocatalysts for industrial synthesis of NMPs, several drawbacks must be overcome before reaching a suitable industrial application. In this sense, multi-enzyme systems provide an appropriate framework for this purpose. Moreover, future advances in different disciplines as protein engineering, bioinformatics and -omics will help to reach this goal.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipFundación Santander
dc.description.sponsorshipUniversidad Europea de Madrid
dc.description.statuspub
dc.identifier.citationDel Arco, & Fernandez-Lucas. (2017). Purine and pyrimidine phosphoribosyltransferases: A versatile tool for enzymatic synthesis of nucleoside-5′-monophosphates [Review of Purine and pyrimidine phosphoribosyltransferases: A versatile tool for enzymatic synthesis of nucleoside-5′-monophosphates]. Current Pharmaceutical Design, 23(45), 6898-6912. Bentham Science Publishers B.V. https://doi.org/10.2174/1381612823666171017165707
dc.identifier.doi10.2174/1381612823666171017165707
dc.identifier.essn1873-4286
dc.identifier.issn1381-6128
dc.identifier.officialurlhttps://www.eurekaselect.com/article/86419
dc.identifier.urihttps://hdl.handle.net/20.500.14352/110830
dc.issue.number45
dc.journal.titleCurrent Pharmaceutical Design
dc.language.isoeng
dc.page.final6912
dc.page.initial6898
dc.publisherBentham Science
dc.relation.projectIDinfo:eu-repo/grantAgreement/Fundación Santander//SAN151610/ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/Universidad Europea de Madrid//2016%2FUEM8/ES
dc.rights.accessRightsrestricted access
dc.subject.cdu577.113.3
dc.subject.cdu577.15
dc.subject.cdu577.123.3
dc.subject.cdu60
dc.subject.cdu66.0
dc.subject.keywordBiocatalysis
dc.subject.keywordNucleic acid derivatives
dc.subject.keywordPhosphoribosyltransferas
dc.subject.keywordNucleosides
dc.subject.keywordNucleoside-5'-monophosphates (NMPs)
dc.subject.ucmBioquímica (Biología)
dc.subject.ucmBiología molecular (Biología)
dc.subject.ucmBiotecnología
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2302.09 Enzimología
dc.subject.unesco2302.23 Ácidos Nucleicos
dc.subject.unesco3303.11 Química Industrial
dc.titlePurine and pyrimidine phosphoribosyltransferases: A versatile tool for enzymatic synthesis of nucleoside-5′-monophosphates
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number23
dspace.entity.typePublication
relation.isAuthorOfPublicationf99cf5b4-0f0d-424c-afd9-77bdedffd366
relation.isAuthorOfPublication.latestForDiscoveryf99cf5b4-0f0d-424c-afd9-77bdedffd366

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