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Pyrophosphate formation as the most efficient condensation reaction of activated nucleotides
Authors:Libaniel Rodriguez  Leslie E. Orgel
Affiliation:(1) The Salk Institute for Biological Studies, P.O. Box 85800, 92122 San Diego, CA, USA
Abstract:Summary When an oligonucleotide primer pG10 is incubated with the nucleotide analogue 9-[3-hydroxy-2-(hydroxymethyl)prop-1-yl] guanine diphosphate ( 
$$poverline{overline G} p$$
, I) in the presence of poly(C), addition of the monomer occurs almost exclusively at the 5′-terminal phosphate rather than the 3′-terminalcis-glycol. The implications of this finding in the context of prebiotic condensation reactions are discussed.
Keywords:Pyrophosphate formation  Template-directed synthesis  Nucleotide analogues
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