Literature DB >> 1667457

High-performance liquid chromatographic determination of pyrophosphate in the presence of a 20,000-fold excess of orthophosphate.

N Yoza1, I Akazaki, T Nakazato, N Ueda, H Kodama, A Tateda.   

Abstract

An HPLC method was based on anion-exchange separation of pyrophosphate (diphosphate) and orthophosphate and postcolumn spectrophotometric detection at 140 degrees C with a molybdenum(V)-molybdenum(VI) reagent. The reagent was easy to prepare, stable for at least 6 months at room temperature, and ready for the determination of pyrophosphate and orthophosphate by the so-called heteropoly blue method without use of any reducing agent. A photodiode-array detector for HPLC indicated the spectral characteristics of the heteropoply blue complex that was detectable at 330-800 nm. The HPLC method had a wide dynamic range from 3 x 10(-7) to 5 x 10(-4) M for both pyrophosphate and orthophosphate with a relative standard deviation of measurement of 10 approximately 2%. Pyrophosphate of 5 x 10(-7) and 5 x 10(-6) M, respectively, could be determined in the presence of a 20,000-fold excess of orthophosphate; 0.01 and 0.1 M.

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Year:  1991        PMID: 1667457     DOI: 10.1016/0003-2697(91)90102-y

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  2 in total

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Authors:  Taisiya A Telegina; Michael P Kolesnikov; Yulia L Vechtomova; Andrey A Buglak; Mikhail S Kritsky
Journal:  J Mol Evol       Date:  2013-05-21       Impact factor: 2.395

2.  Metabolic profiling of alternative NAD biosynthetic routes in mouse tissues.

Authors:  Valerio Mori; Adolfo Amici; Francesca Mazzola; Michele Di Stefano; Laura Conforti; Giulio Magni; Silverio Ruggieri; Nadia Raffaelli; Giuseppe Orsomando
Journal:  PLoS One       Date:  2014-11-25       Impact factor: 3.240

  2 in total

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