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Synthesis and enzymatic evaluation of the guanosine analogue 2-amino-6-mercapto-7-methylpurine ribonucleoside (MESG): insights into the phosphorolysis reaction mechanism based on the blueprint transition state: SN1 or SN2?

By Brenno A.D. Neto, Alexandre A.M. Lapis, Paulo A. Netz, John Spencer, Silvio L.P. Dias, Silvia M. Tamborim, Luiz A. Basso, Diógenes S. Santos and Jairton Dupont

Abstract

A modified experimental procedure for the synthesis of MESG (2-amino-6-mercapto-7-methylpurine ribonucleoside) 1 has been successfully performed and its full characterization is presented. High resolution ESI(+)-MSMS indicates both the nucleoside bond cleavage as the main fragmentation in the gas phase and a possible SN1 mechanism. Ab initio transition state calculations based on the blue print transition state support this mechanistic rationale and discard an alternative SN2 mechanism. Assays using purine nucleoside phosphorylase (PNP) enzyme (human and M. tuberculosis sources) indicate its efficiency in the phosphorolysis of MESG and allow the quantitative determination of inorganic phosphate in real time assay

Topics: QD
Publisher: Sociedade Brasileira de Quimica
Year: 2010
OAI identifier: oai:gala.gre.ac.uk:2084

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