Salvage pathway for NAD biosynthesis in Brevibacterium ammoniagenes: Regulatory properties of triphosphate-dependent nicotinate phosphoribosyltransferase

Natalia Dulianinova, Elena M. Podlepa, Larisa V. Toulokhonova, Vladimir Ya Bykhovsky

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

As the rate-limiting enzyme, catalyzing the first reaction in NAD salvage synthesis, nicotinate phosphoribosyltransferase (NAPRTase, EC 2.4.2.11) is of important interest for studies of intracellular pyridine nucleotide pool regulation. We have purified NAPRTase 520-fold from Brevibacterium ammoniagenes ATCC 6872 without using an over-expression system by applying acid treatment, salt fractionation, Ca-phosphate gel treatment, anion exchange column chromatography and size-exclusion gel filtration. Unlike this enzyme from other sources, B. ammoniagenes NAPRTase was found to be controlled by the feedback inhibition by the end product NAD with K(i)=0.7±0.1 mM. The reaction products, pyrophosphate and nicotinate mononucleotide, also decreased the enzyme activity, as did other intermediates of NAD synthesis, such as AMP, ADP and a NAD direct precursor, nicotinate adenine dinucleotide or deamido NAD. The enzyme was observed to require a nucleoside triphosphate for its activity and showed the maximum affinity for ATP. The specificity, however, turned out to be poor, and ATP could be substituted by other nucleoside triphosphates as well as by sodium triphosphate. The kinetic characteristics of the enzyme are reported. For the first time, our data have experimentally revealed such complicated stimulatory and inhibitory effects by the intermediates of NAD biosynthesis on one of its salvage enzymes, NAPRTase. On the basis of these data, the key role of NAPRTase is discussed in light of the regulation of NAD metabolism in B. ammoniagenes. Copyright (C) 1998 Elsevier Science B.V.

Original languageEnglish (US)
Pages (from-to)211-220
Number of pages10
JournalBiochimica et Biophysica Acta - Protein Structure and Molecular Enzymology
Volume1478
Issue number2
DOIs
StatePublished - May 23 2000
Externally publishedYes

Fingerprint

Brevibacterium
Salvaging
Biosynthesis
NAD
Enzymes
Nucleosides
Gel Chromatography
Adenosine Triphosphate
Gels
Column chromatography
Niacin
Enzyme activity
Adenine
Adenosine Monophosphate
Fractionation
Reaction products
Metabolism
Adenosine Diphosphate
Anions
triphosphoric acid

Keywords

  • Brevibacterium ammoniagenes
  • Enzyme kinetics
  • Feed-back inhibition
  • NAD metabolism
  • Nicotinate phosphoribosyltransferase
  • Salvage pathway

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Structural Biology
  • Biophysics

Cite this

Salvage pathway for NAD biosynthesis in Brevibacterium ammoniagenes : Regulatory properties of triphosphate-dependent nicotinate phosphoribosyltransferase. / Dulianinova, Natalia; Podlepa, Elena M.; Toulokhonova, Larisa V.; Bykhovsky, Vladimir Ya.

In: Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology, Vol. 1478, No. 2, 23.05.2000, p. 211-220.

Research output: Contribution to journalArticle

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