Issue 6, 1999

1H and 31P NMR study of ADP and GDP spontaneous synthesis from 2-methylimidazole-activated AMP and GMP nucleotides and inorganic phosphate

Abstract

1 H and 31P NMR data show that adenosine 5′-(2-methylimidazol-1-ylphosphonate) (2-MeImpA) and guanosine 5′-(2-methylimidazol-1-ylphosphonate) (2-MeImpG), known as possible prebiotic precursors of polynucleotides, produce the corresponding diphosphonucleotides in sodium phosphate solution at pD 7.6. Phosphate ions also enhance the hydrolysis of these molecules by activating a water molecular associated as a weak complex with the phosphoryl moiety of 2-MeImpA and 2-MeImpG. A kinetic study was done by quantitative 1H NMR spectroscopy and mechanistic hypotheses were tested by semiempirical PM3 modelling.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1999, 1143-1148

1 H and 31P NMR study of ADP and GDP spontaneous synthesis from 2-methylimidazole-activated AMP and GMP nucleotides and inorganic phosphate

J. Pereira and A. Cadete, J. Chem. Soc., Perkin Trans. 2, 1999, 1143 DOI: 10.1039/A900884E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements