dc.creatorFernández-Lucas, Jesús
dc.date2021-10-04T19:43:32Z
dc.date2021-10-04T19:43:32Z
dc.date2021-08-03
dc.date.accessioned2023-10-03T20:12:04Z
dc.date.available2023-10-03T20:12:04Z
dc.identifier2218-273X
dc.identifierhttps://hdl.handle.net/11323/8774
dc.identifierhttps://doi.org/10.3390/biom11081147
dc.identifierCorporación Universidad de la Costa
dc.identifierREDICUC - Repositorio CUC
dc.identifierhttps://repositorio.cuc.edu.co/
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/9174768
dc.descriptionNucleic acid derivatives are involved in cell growth and replication, but they are also particularly important as building blocks for RNA and DNA synthesis. In nature, purine and pyrimidine nucleotides are synthesized through two distinct pathways, de novo and salvage pathways, both depending on 5-phospho-α-D-ribose 1-diphosphate (PRPP) as a key element [1,2]. In the de novo pathway, purine and pyrimidine nucleotides are synthesized from simple molecules such as glycine, glutamine, or aspartate. In contrast, the salvage pathway employs scavenged preformed endogenous or exogenous nucleobases to generate the corresponding nucleoside-50 -monophosphates (NMPs) [3]. Both metabolic routes, de novo and salvage pathways, lead to the synthesis of NMPs, which are subsequently phosphorylated to obtain the corresponding nucleoside-50 -di (NDPs) and triphosphates (NTPs). Moreover, all organisms also generate (20 -deoxy)nucleoside-50 -diphosphates (dNDPs) from NDPs [4], which will be converted to 20 -deoxyribonucleotides (dNTPs), as precursors for DNA synthesis. Additionally, nucleotide derivatives are involved in cell signaling (cyclic nucleotides, cNMPs or c-di-NMPs) [5] and a multitude of different biochemical processes, acting as cofactors (NADP+ ) or energy sources (ATP).
dc.formatapplication/pdf
dc.formatapplication/pdf
dc.languageeng
dc.publisherCorporación Universidad de la Costa
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dc.relation6. Parker, W.B. Enzymology of purine and pyrimidine antimetabolites used in the treatment of cancer. Chem. Rev. 2009, 109, 2880–2893. [CrossRef] [PubMed]
dc.relation7. Fernández-Lucas, J.; Camarasa, M.J. (Eds.) Enzymatic and Chemical Synthesis of Nucleic Acid Derivatives; John Wiley & Sons: Hoboken, NJ, USA, 2019. [CrossRef]
dc.relation8. Kayushin, A.L.; Tokunova, J.A.; Fateev, I.V.; Arnautova, A.O.; Berzina, M.Y.; Paramonov, A.S.; Lutonina, O.I.; Dorofeeva, E.V.; Antonov, K.V.; Esipov, R.S.; et al. Radical dehalogenation and purine nucleoside phosphorylase E. coli: How does an admixture of 20, 30 -anhydroinosine hinder 2-fluoro-cordycepin synthesis. Biomolecules 2021, 11, 539. [CrossRef] [PubMed]
dc.relation9. Rivero, C.W.; García, N.S.; Fernández-Lucas, J.; Betancor, L.; Romanelli, G.P.; Trelles, J.A. Green production of cladribine by using immobilized 20 -deoxyribosyltransferase from Lactobacillus delbrueckii stabilized through a double covalent/entrapment technology. Biomolecules 2021, 11, 657. [CrossRef] [PubMed]
dc.relation10. Sverkeli, L.J.; Hayat, F.; Migaud, M.E.; Ziegler, M. Enzymatic and chemical syntheses of vacor analogs of nicotinamide riboside, NMN and NAD. Biomolecules 2021, 11, 1044. [CrossRef]
dc.relation11. Fateev, I.V.; Kostromina, M.A.; Abramchik, Y.A.; Eletskaya, B.Z.; Mikheeva, O.O.; Lukoshin, D.D.; Zayats, E.A.; Berzina, M.Y.; Dorofeeva, E.V.; Paramonov, A.S.; et al. Multi-enzymatic cascades in the synthesis of modified nucleosides: Comparison of the thermophilic and mesophilic pathways. Biomolecules 2021, 11, 586. [CrossRef] [PubMed]
dc.relation12. Frisch, J.; Marši´c, T.; Loderer, C.A. Novel one-pot enzyme cascade for the biosynthesis of cladribine triphosphate. Biomolecules 2021, 11, 346. [CrossRef] [PubMed]
dc.relation13. Becker, M.; Nikel, P.; Andexer, J.N.; Lütz, S.; Rosenthal, K.A. Multi-enzyme cascade reaction for the production of 2’3’-cGAMP. Biomolecules 2021, 11, 590. [CrossRef] [PubMed]
dc.relation14. Acosta, J.; Pérez, E.; Sánchez-Murcia, P.A.; Fillat, C.; Fernández-Lucas, J. Molecular basis of ndt-mediated activation of nucleosidebased prodrugs and application in suicide gene therapy. Biomolecules 2021, 11, 120. [CrossRef] [PubMed]
dc.rightsCC0 1.0 Universal
dc.rightshttp://creativecommons.org/publicdomain/zero/1.0/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.sourceBiomolecules
dc.sourcehttps://www.mdpi.com/2218-273X/11/8/1147
dc.subjectBiotechnological applications
dc.subjectBiomedical applications
dc.subjectNucleosides
dc.subjectNucleotides
dc.titleBiotechnological and biomedical applications of enzymes involved in the synthesis of nucleosides and nucleotides
dc.typeArtículo de revista
dc.typehttp://purl.org/coar/resource_type/c_6501
dc.typeText
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typehttp://purl.org/redcol/resource_type/ART
dc.typeinfo:eu-repo/semantics/acceptedVersion
dc.typehttp://purl.org/coar/version/c_ab4af688f83e57aa


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