Literature DB >> 18845122

Reduction of porphyrins to porphyrinogens with palladium on carbon.

Hector A Bergonia1, John D Phillips, James P Kushner.   

Abstract

Porphyrinogens serve as substrates for three heme biosynthetic enzymes. Porphyrinogens are highly unstable and must be generated as an integral part of enzyme assays. Methods commonly employed to generate porphyrinogens include chemical reduction using sodium amalgam or sodium borohydride and enzymatic generation from porphobilinogen. Chemical reduction yields porphyrinogens in highly alkaline solutions with high ionic strength, whereas enzymatic generation requires purified enzymes, deproteination, and complete buffer replacement. This article describes an improved method for reducing porphyrins to porphyrinogens using palladium on carbon as a catalyst under hydrogen at ambient temperature and pressure in the dark. The palladium catalyst is removed by filtration, the filtrate is blown dry with an inert gas, and the dried porphyrinogen can be dissolved in a buffer compatible with biological studies.

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Year:  2008        PMID: 18845122      PMCID: PMC2658817          DOI: 10.1016/j.ab.2008.09.027

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


  5 in total

1.  Crystal structure of human uroporphyrinogen III synthase.

Authors:  M A Mathews; H L Schubert; F G Whitby; K J Alexander; K Schadick; H A Bergonia; J D Phillips; C P Hill
Journal:  EMBO J       Date:  2001-11-01       Impact factor: 11.598

Review 2.  Palladium--a review of exposure and effects to human health.

Authors:  Janet Kielhorn; Christine Melber; Detlef Keller; Inge Mangelsdorf
Journal:  Int J Hyg Environ Health       Date:  2002-10       Impact factor: 5.840

3.  Structural basis for tetrapyrrole coordination by uroporphyrinogen decarboxylase.

Authors:  John D Phillips; Frank G Whitby; James P Kushner; Christopher P Hill
Journal:  EMBO J       Date:  2003-12-01       Impact factor: 11.598

4.  Uroporphyrinogen decarboxylase. A method for measuring enzyme activity.

Authors:  J G Straka; J P Kushner; M A Pryor
Journal:  Enzyme       Date:  1982

5.  A porphomethene inhibitor of uroporphyrinogen decarboxylase causes porphyria cutanea tarda.

Authors:  John D Phillips; Hector A Bergonia; Christopher A Reilly; Michael R Franklin; James P Kushner
Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-09       Impact factor: 11.205

  5 in total
  3 in total

1.  Heme biosynthesis is coupled to electron transport chains for energy generation.

Authors:  Kalle Möbius; Rodrigo Arias-Cartin; Daniela Breckau; Anna-Lena Hännig; Katrin Riedmann; Rebekka Biedendieck; Susanne Schröder; Dörte Becher; Axel Magalon; Jürgen Moser; Martina Jahn; Dieter Jahn
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-19       Impact factor: 11.205

2.  Substrate shuttling between active sites of uroporphyrinogen decarboxylase is not required to generate coproporphyrinogen.

Authors:  John D Phillips; Christy A Warby; Frank G Whitby; James P Kushner; Christopher P Hill
Journal:  J Mol Biol       Date:  2009-04-10       Impact factor: 5.469

3.  From porphyrin benzylphosphoramidate conjugates to the catalytic hydrogenation of 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin.

Authors:  Marcos C de Souza; Leandro F Pedrosa; Géssica S Cazagrande; Vitor F Ferreira; Maria G P M S Neves; José A S Cavaleiro
Journal:  Beilstein J Org Chem       Date:  2014-03-10       Impact factor: 2.883

  3 in total

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