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• W2045409118 abstract "The identification of the nucleoside liberated by the action of spleen or snake venom phos‐phodiesterase on dephosphorylated dinucleosidemonophosphates directly reveals whether the nucleoside participates in the phosphodiester bond with its 3′‐ or 5′‐hydroxyl. We report a sensitive direct Spectrophotometric procedure for the detection and estimation of the liberated nucleoside, based on the following specific enzyme systems: guanosine phosphorylase, guanase and xanthine oxidase for guanosine at 290 nm, adenosine deaminase for adenosine at 265 run; cytidine deaminase for cytidine at 280 nm and uridine phosphorylase for uridine at 282 nm. The structure of dinucleotides is determined in single experiments: the liberated nucleoside bearing the free 3′‐ or 5′‐hydroxyl is identified and quantitatively measured by its response to one of the ancillary systems; the remaining 5′‐ or 3′‐mononucleotide is identified as nucleoside after addition of phosphomonoesterase. The use of T1 and pancreatic ribonucleases, along with the proposed principles and techniques, in studying the sequence of trinucleotides and tetranucleotides is discussed in the Appendix." @default.
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• W2045409118 date "1970-12-01" @default.
• W2045409118 modified "2023-10-02" @default.
• W2045409118 title "Direct Spectrophotometric Determination of the Structure of Dinucleoside Monophosphates" @default.
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• W2045409118 doi "https://doi.org/10.1111/j.1432-1033.1970.tb01197.x" @default.
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