Biomolecules (Mar 2020)

Hydroxylamine Analogue of Agmatine: Magic Bullet for Arginine Decarboxylase

  • Mervi T. Hyvönen,
  • Tuomo A. Keinänen,
  • Gulgina K. Nuraeva,
  • Dmitry V. Yanvarev,
  • Maxim Khomutov,
  • Elena N. Khurs,
  • Sergey N. Kochetkov,
  • Jouko Vepsäläinen,
  • Alexander A. Zhgun,
  • Alex R. Khomutov

DOI
https://doi.org/10.3390/biom10030406
Journal volume & issue
Vol. 10, no. 3
p. 406

Abstract

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The biogenic polyamines, spermine, spermidine (Spd) and putrescine (Put) are present at micro-millimolar concentrations in eukaryotic and prokaryotic cells (many prokaryotes have no spermine), participating in the regulation of cellular proliferation and differentiation. In mammalian cells Put is formed exclusively from L-ornithine by ornithine decarboxylase (ODC) and many potent ODC inhibitors are known. In bacteria, plants, and fungi Put is synthesized also from agmatine, which is formed from L-arginine by arginine decarboxylase (ADC). Here we demonstrate that the isosteric hydroxylamine analogue of agmatine (AO-Agm) is a new and very potent (IC50 3•10-8 M) inhibitor of E. coli ADC. It was almost two orders of magnitude less potent towards E. coli ODC. AO-Agm decreased polyamine pools and inhibited the growth of DU145 prostate cancer cells only at high concentration (1 mM). Growth inhibitory analysis of the Acremonium chrysogenum demonstrated that the wild type (WT) strain synthesized Put only from L-ornithine, while the cephalosporin C high-yielding strain, in which the polyamine pool is increased, could use both ODC and ADC to produce Put. Thus, AO-Agm is an important addition to the set of existing inhibitors of the enzymes of polyamine biosynthesis, and an important instrument for investigating polyamine biochemistry.

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